Item | Value |
---|---|
geneid | 256714 |
ensemblid | ENSG00000184368.16 |
hgncid | 25899 |
symbol | MAP7D2 |
name | MAP7 domain containing 2 |
refseq_nuc | NM_001168465.2 |
refseq_prot | NP_001161937.1 |
ensembl_nuc | ENST00000379643.10 |
ensembl_prot | ENSP00000368964.5 |
mane_status | MANE Select |
chr | chrX |
start | 20006713 |
end | 20116907 |
strand | - |
ver | v1.2 |
region | chrX:20006713-20116907 |
region5000 | chrX:20001713-20121907 |
regionname0 | MAP7D2_chrX_20006713_20116907 |
regionname5000 | MAP7D2_chrX_20001713_20121907 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 773 | 104 | 2 | 23 | 60 | 4 | 13 | 45 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002 | 0/0 | 773 | 97 | 62 | 19 | 8 | 3 | 5 | 7 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0003 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0004 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0005 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0006 | 0/0 | 689 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0007 | 0/0 | 689 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0008 | 0/0 | 773 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0009 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0010 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0011 | 0/0 | 773 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2322 | 103 | 1 | 23 | 60 | 4 | 13 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0002 | 0/0 | 2322 | 79 | 51 | 15 | 7 | 3 | 3 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0003 | 0/0 | 2322 | 9 | 6 | 0 | 1 | 0 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0004 | 0/0 | 2322 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0005 | 0/0 | 2322 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0006 | 0/0 | 2322 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0007 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0008 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0009 | 0/0 | 2327 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0010 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0011 | 0/0 | 2326 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0012 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0013 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0014 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0015 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
c0016 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1741 | 194 | 59 | 40 | 70 | 7 | 16 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0002 | 0/0 | 1741 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0003 | 0/0 | 1741 | 4 | 0 | 0 | 1 | 0 | 3 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0004 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0005 | 0/0 | 1741 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0006 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0007 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0008 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0009 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
t0010 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2322 | 103 | 1 | 23 | 60 | 4 | 13 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0001c0013 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0002 | 0/0 | 2322 | 79 | 51 | 15 | 7 | 3 | 3 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0003 | 0/0 | 2322 | 9 | 6 | 0 | 1 | 0 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0004 | 0/0 | 2322 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0005 | 0/0 | 2322 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0014 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0003c0016 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0004c0011 | 0/0 | 2326 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0005c0010 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0006c0008 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0007c0007 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0008c0006 | 0/0 | 2322 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0009c0009 | 0/0 | 2327 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0010c0015 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0011c0012 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4062 | 101 | 1 | 21 | 60 | 4 | 13 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0001c0001t0004 | 0/0 | 4064 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0001c0001t0005 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0001c0013t0001 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0002t0001 | 0/0 | 4062 | 72 | 46 | 14 | 7 | 3 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0002t0002 | 0/0 | 4062 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0002t0003 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0002t0010 | 0/0 | 4085 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0003t0001 | 0/0 | 4062 | 5 | 5 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0003t0003 | 0/0 | 4062 | 3 | 0 | 0 | 1 | 0 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0003t0007 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0004t0001 | 0/0 | 4062 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0005t0001 | 0/0 | 4062 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0002c0014t0001 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0003c0016t0009 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0004c0011t0006 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0005c0010t0001 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0006c0008t0001 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0007c0007t0001 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0008c0006t0001 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0009c0009t0001 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0010c0015t0008 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
a0011c0012t0001 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | copy fasta | chrX | 20001713 | 20121907 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0001c0013t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0002t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0003t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0002c0014t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0003c0016t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0004c0011t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0005c0010t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0006c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0007c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0008c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0009c0009t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0010c0015t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
a0011c0012t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00735 | hp1 | a0011 | c0012 | t0001 | g0120 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01106 | hp1 | a0002 | c0004 | t0001 | g0174 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01256 | hp1 | a0002 | c0005 | t0001 | g0121 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01346 | hp2 | a0002 | c0014 | t0001 | g0161 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01496 | hp2 | a0002 | c0005 | t0001 | g0122 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0159 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0160 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01891 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02015 | hp1 | a0002 | c0003 | t0003 | g0095 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02145 | hp1 | a0002 | c0003 | t0007 | g0103 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02257 | hp1 | a0001 | c0013 | t0001 | g0190 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0206 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0186 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0113 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02897 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0202 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03017 | hp1 | a0002 | c0003 | t0003 | g0094 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03195 | hp2 | a0002 | c0004 | t0001 | g0172 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0173 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03486 | hp1 | a0005 | c0010 | t0001 | g0107 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03490 | hp1 | a0002 | c0003 | t0003 | g0096 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03654 | hp1 | a0008 | c0006 | t0001 | g0060 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0156 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18974 | hp1 | a0007 | c0007 | t0001 | g0104 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18989 | hp1 | a0009 | c0009 | t0001 | g0020 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19030 | hp2 | a0002 | c0002 | t0010 | g0209 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19060 | hp1 | a0006 | c0008 | t0001 | g0061 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19067 | hp1 | a0010 | c0015 | t0008 | g0165 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19076 | hp1 | a0004 | c0011 | t0006 | g0004 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | ASW | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ASW | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0157 | EUR | TSI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0070 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02109 | hp1 | a0002 | c0005 | t0001 | g0123 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
HG06807 | hp2 | a0003 | c0016 | t0009 | g0208 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:20010951 | CG | C | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.2173delC | p.Arg725fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/17 | 2201/4062 | 2173/2322 | 725/773 | chrX | 20010951 | ||
chrX:20012429 | TC | T | 1 | a0006 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.1991delG | p.Gly664fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/17 | 2019/4062 | 1991/2322 | 664/773 | chrX | 20012429 | ||
chrX:20012480 | TG | T | 1 | a0007 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.1940delC | p.Pro647fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/17 | 1968/4062 | 1940/2322 | 647/773 | chrX | 20012480 | ||
chrX:20012488 | C | T | 1 | a0008 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1933G>A | p.Ala645Thr | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/17 | 1961/4062 | 1933/2322 | 645/773 | chrX | 20012488 | ||
chrX:20016118 | T | TTG | 1 | a0009 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.1618_1619dupCA | p.Gln540fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1647/4062 | 1619/2322 | 540/773 | chrX | 20016118 | ||
chrX:20016137 | T | TC | 1 | a0009 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.1600_1601insG | p.Lys534fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1628/4062 | 1600/2322 | 534/773 | chrX | 20016137 | ||
chrX:20016203 | T | TC | 1 | a0009 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.1534dupG | p.Glu512fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1562/4062 | 1534/2322 | 512/773 | chrX | 20016203 | ||
chrX:20016217 | T | TC | 1 | a0009 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.1520_1521insG | p.Gln509fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1548/4062 | 1520/2322 | 507/773 | chrX | 20016217 | ||
chrX:20016221 | T | C | 1 | a0009 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.1517A>G | p.Lys506Arg | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1545/4062 | 1517/2322 | 506/773 | chrX | 20016221 | ||
chrX:20025005 | C | CG | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1357dupC | p.Arg453fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/17 | 1385/4062 | 1357/2322 | 453/773 | chrX | 20025005 | ||
chrX:20025699 | T | TC | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1260dupG | p.Lys421fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1288/4062 | 1260/2322 | 420/773 | chrX | 20025699 | ||
chrX:20025854 | T | TC | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1105dupG | p.Asp369fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1133/4062 | 1105/2322 | 369/773 | chrX | 20025854 | ||
chrX:20025866 | A | AG | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1093dupC | p.Leu365fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1121/4062 | 1093/2322 | 365/773 | chrX | 20025866 | ||
chrX:20025950 | G | A | 1 | a0005 | 1 | HG03486.hp1 | missense_variant&splice_region_variant | MODERATE | c.1010C>T | p.Thr337Ile | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1038/4062 | 1010/2322 | 337/773 | chrX | 20025950 | ||
chrX:20025951 | T | TC | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant&splice_region_variant | HIGH | c.1008dupG | p.Thr337fs | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1036/4062 | 1008/2322 | 336/773 | chrX | 20025951 | ||
chrX:20042517 | G | A | 1 | a0010 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.992C>T | p.Ser331Phe | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/17 | 1020/4062 | 992/2322 | 331/773 | chrX | 20042517 | ||
chrX:20052928 | T | C | 3 | a0002a0003a0010 | 99 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(96): Show |
missense_variant | MODERATE | c.545A>G | p.Asn182Ser | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/17 | 573/4062 | 545/2322 | 182/773 | chrX | 20052928 | ||
chrX:20116759 | G | A | 1 | a0011 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.121C>T | p.Arg41Trp | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 149/4062 | 121/2322 | 41/773 | chrX | 20116759 | ||
chrX:20116839 | G | A | 1 | a0003 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.41C>T | p.Pro14Leu | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 69/4062 | 41/2322 | 14/773 | chrX | 20116839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:20016220 | C | T | 1 | a0009c0009 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1518G>A | p.Lys506Lys | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1546/4062 | 1518/2322 | 506/773 | chrX | 20016220 | ||
chrX:20044412 | A | T | 1 | a0002c0014 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.831T>A | p.Gly277Gly | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/17 | 859/4062 | 831/2322 | 277/773 | chrX | 20044412 | ||
chrX:20056693 | G | A | 2 | a0002c0004a0003c0016 | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.471C>T | p.Pro157Pro | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/17 | 499/4062 | 471/2322 | 157/773 | chrX | 20056693 | ||
chrX:20116784 | C | G | 1 | a0002c0005 | 3 | HG01256.hp1 HG01496.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.96G>C | p.Ala32Ala | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 124/4062 | 96/2322 | 32/773 | chrX | 20116784 | ||
chrX:20116862 | G | A | 7 | a0001c0013a0002c0002a0002c0004others(4): Show | 91 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(88): Show |
synonymous_variant | LOW | c.18C>T | p.Gly6Gly | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 46/4062 | 18/2322 | 6/773 | chrX | 20116862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:20006778 | T | C | 1 | a0001c0001t0005 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 4025 | chrX | 20006778 | |||||
chrX:20007484 | G | GC | 1 | a0001c0001t0004 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 3318 | chrX | 20007484 | |||||
chrX:20007527 | GT | G | 1 | a0004c0011t0006 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 3275 | chrX | 20007527 | |||||
chrX:20007876 | A | AT | 1 | a0001c0001t0004 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2926 | chrX | 20007876 | |||||
chrX:20007987 | T | C | 1 | a0002c0003t0007 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2816 | chrX | 20007987 | |||||
chrX:20008014 | T | TA | 1 | a0010c0015t0008 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2788 | chrX | 20008014 | |||||
chrX:20008153 | C | G | 1 | a0002c0002t0002 | 5 | HG01070.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*272G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2650 | chrX | 20008153 | |||||
chrX:20008166 | A | G | 2 | a0002c0002t0003a0002c0003t0003 | 4 | HG02015.hp1 HG03017.hp1 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*259T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2637 | chrX | 20008166 | |||||
chrX:20116881 | G | A | 1 | a0003c0016t0009 | 1 | HG06807.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-2C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | chrX | 20116881 | ||||||
chrX:20116886 | G | GCGCCGGC others(16): Show |
1 | a0002c0002t0010 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8_-7insGCAGTGCGCC others(13): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 8 | chrX | 20116886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:20008677 | G | GC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*27-280dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20008677 | ||||||
chrX:20009075 | A | AG | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.*27-678dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009075 | ||||||
chrX:20009174 | T | C | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*27-776A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009174 | ||||||
chrX:20009221 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.*27-823A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009221 | ||||||
chrX:20009287 | T | C | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.*27-889A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009287 | ||||||
chrX:20009346 | GC | G | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*27-949delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009346 | ||||||
chrX:20009383 | G | GC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*27-986dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009383 | ||||||
chrX:20009663 | C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0033others(19): Show | 23 | HG01071.hp1 HG01256.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.*26+1113dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | ||||||
chrX:20009663 | C | CAA | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.*26+1112_*26+1113d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | ||||||
chrX:20009663 | CA | C | 42 | a0001c0001t0001g0031a0001c0001t0001g0047a0002c0002t0001g0125others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.*26+1113delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | ||||||
chrX:20009663 | CAA | C | 1 | a0002c0002t0001g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*26+1112_*26+1113d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | ||||||
chrX:20009663 | CAAAAAAA others(5): Show |
C | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*26+1102_*26+1113d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | ||||||
chrX:20009753 | TG | T | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*26+1023delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009753 | ||||||
chrX:20009803 | C | CG | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.*26+973dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009803 | ||||||
chrX:20009838 | TA | T | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.*26+938delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009838 | ||||||
chrX:20009989 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*26+788G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009989 | ||||||
chrX:20010043 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.*26+734T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010043 | ||||||
chrX:20010166 | A | G | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.*26+611T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010166 | ||||||
chrX:20010318 | TG | T | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*26+458delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010318 | ||||||
chrX:20010475 | GC | G | 85 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(82): Show | 86 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.*26+301delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010475 | ||||||
chrX:20010647 | AC | A | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*26+129delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010647 | ||||||
chrX:20011067 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2073-15G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011067 | ||||||
chrX:20011275 | GA | G | 11 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2073-224delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011275 | ||||||
chrX:20011635 | G | GT | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2073-584dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011635 | ||||||
chrX:20011638 | A | AAGGT | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2073-590_2073-587d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011638 | ||||||
chrX:20011783 | C | G | 11 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2072+566G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011783 | ||||||
chrX:20011804 | TC | T | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2072+544delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011804 | ||||||
chrX:20011810 | G | GA | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2072+538dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011810 | ||||||
chrX:20011950 | C | CT | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2072+398dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011950 | ||||||
chrX:20012021 | C | A | 5 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(2): Show | 5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072+328G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012021 | ||||||
chrX:20012048 | TC | T | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2072+300delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012048 | ||||||
chrX:20012073 | T | A | 57 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0133others(54): Show | 57 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2072+276A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012073 | ||||||
chrX:20012097 | T | TC | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2072+251dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012097 | ||||||
chrX:20012117 | TC | T | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2072+231delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012117 | ||||||
chrX:20012202 | G | C | 1 | a0002c0002t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2072+147C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012202 | ||||||
chrX:20012206 | GT | G | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2072+142delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012206 | ||||||
chrX:20012215 | CTGAGAG | C | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2072+128_2072+133d others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012215 | ||||||
chrX:20012268 | TA | T | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2072+80delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012268 | ||||||
chrX:20012558 | T | C | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1886-23A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012558 | ||||||
chrX:20012664 | GC | G | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1886-130delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012664 | ||||||
chrX:20012858 | TA | T | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1885+195delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012858 | ||||||
chrX:20012860 | A | C | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1885+194T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012860 | ||||||
chrX:20012910 | A | AG | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1885+143dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012910 | ||||||
chrX:20012918 | TC | T | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1885+135delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012918 | ||||||
chrX:20013030 | CCAAGA | C | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1885+19_1885+23del others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20013030 | ||||||
chrX:20013275 | TC | T | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1807-144delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 13/16 | chrX | 20013275 | ||||||
chrX:20013461 | A | AT | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1806+107dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 13/16 | chrX | 20013461 | ||||||
chrX:20013633 | C | CA | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1750-9dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013633 | ||||||
chrX:20013739 | A | C | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-114T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013739 | ||||||
chrX:20013825 | C | T | 10 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(7): Show | 10 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1750-200G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013825 | ||||||
chrX:20013839 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1750-214A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013839 | ||||||
chrX:20013863 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1750-238G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013863 | ||||||
chrX:20014013 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750-388A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014013 | ||||||
chrX:20014253 | G | A | 2 | a0002c0002t0001g0154a0002c0002t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1750-628C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014253 | ||||||
chrX:20014523 | A | G | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1749+700T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014523 | ||||||
chrX:20014843 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1749+380G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014843 | ||||||
chrX:20015013 | C | G | 94 | a0001c0001t0001g0087a0002c0002t0001g0001a0002c0002t0001g0125others(91): Show | 95 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1749+210G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20015013 | ||||||
chrX:20015583 | G | C | 1 | a0002c0002t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1645-256C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20015583 | ||||||
chrX:20015613 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1645-286C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20015613 | ||||||
chrX:20016054 | T | C | 2 | a0002c0002t0001g0151a0002c0002t0001g0166 | 2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1644+40A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20016054 | ||||||
chrX:20016401 | C | CGA | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-78_1413-77dup others(2): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016401 | ||||||
chrX:20016553 | A | G | 15 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413-228T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016553 | ||||||
chrX:20016611 | A | AG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-287_1413-286i others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016611 | ||||||
chrX:20016626 | C | CT | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-302_1413-301i others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016626 | ||||||
chrX:20016849 | C | CA | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-525dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016849 | ||||||
chrX:20017335 | A | G | 15 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413-1010T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017335 | ||||||
chrX:20017446 | T | TA | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1122dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017446 | ||||||
chrX:20017502 | G | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1177C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017502 | ||||||
chrX:20017511 | T | TG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1187dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017511 | ||||||
chrX:20017701 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1413-1376A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017701 | ||||||
chrX:20017821 | T | TA | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1497_1413-149 others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017821 | ||||||
chrX:20017843 | G | A | 72 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0133others(69): Show | 72 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.1413-1518C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017843 | ||||||
chrX:20017934 | T | TCTTCATC others(4): Show |
1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1620_1413-161 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017934 | ||||||
chrX:20017965 | C | CT | 5 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0084others(2): Show | 5 | HG01981.hp1 NA18979.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413-1641dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | ||||||
chrX:20017965 | CT | C | 14 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0081others(11): Show | 14 | HG01069.hp1 HG01256.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1413-1641delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | ||||||
chrX:20017965 | CTT | C | 65 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0133others(62): Show | 65 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1413-1642_1413-164 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | ||||||
chrX:20017965 | CTTT | C | 2 | a0002c0002t0001g0166a0002c0004t0001g0174 | 2 | HG01106.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1413-1643_1413-164 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | ||||||
chrX:20017965 | CTTTT | C | 4 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0202others(1): Show | 4 | HG02630.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-1644_1413-164 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | ||||||
chrX:20018003 | G | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1678C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018003 | ||||||
chrX:20018171 | G | A | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413-1846C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018171 | ||||||
chrX:20018217 | CG | C | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1893delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018217 | ||||||
chrX:20018440 | C | CT | 10 | a0001c0001t0001g0078a0001c0001t0001g0119a0002c0002t0001g0001others(7): Show | 11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413-2116dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | ||||||
chrX:20018440 | C | CTT | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2117_1413-211 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | ||||||
chrX:20018440 | CT | C | 67 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0004g0016others(64): Show | 67 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1413-2116delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | ||||||
chrX:20018440 | CTT | C | 2 | a0002c0002t0001g0166a0002c0002t0002g0139 | 2 | HG01070.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1413-2117_1413-211 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | ||||||
chrX:20018579 | A | G | 3 | a0002c0002t0001g0125a0002c0002t0001g0145a0002c0002t0001g0170 | 3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1413-2254T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018579 | ||||||
chrX:20019000 | AAGTT | A | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2679_1413-267 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019000 | ||||||
chrX:20019025 | C | CT | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2701dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019025 | ||||||
chrX:20019025 | CT | C | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1413-2701delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019025 | ||||||
chrX:20019103 | T | TGCA | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2781_1413-277 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019103 | ||||||
chrX:20019129 | C | T | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1413-2804G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019129 | ||||||
chrX:20019215 | A | AG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2891dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019215 | ||||||
chrX:20019238 | A | AG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2914dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019238 | ||||||
chrX:20019256 | TG | T | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-2932delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019256 | ||||||
chrX:20019372 | AC | A | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-3048delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019372 | ||||||
chrX:20019379 | T | TC | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-3055dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019379 | ||||||
chrX:20019478 | T | TG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-3154dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019478 | ||||||
chrX:20019538 | G | GC | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-3214dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019538 | ||||||
chrX:20019694 | A | G | 13 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(10): Show | 13 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1413-3369T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019694 | ||||||
chrX:20019705 | T | TTGATC | 13 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(10): Show | 13 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1413-3385_1413-338 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019705 | ||||||
chrX:20019818 | G | A | 2 | a0002c0002t0001g0147a0002c0002t0001g0192 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1413-3493C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019818 | ||||||
chrX:20019851 | A | AG | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-3527dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019851 | ||||||
chrX:20020105 | G | T | 1 | a0002c0002t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1413-3780C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020105 | ||||||
chrX:20020193 | T | A | 1 | a0001c0001t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1413-3868A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020193 | ||||||
chrX:20020353 | C | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-4028G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020353 | ||||||
chrX:20020453 | T | G | 5 | a0002c0002t0001g0194a0002c0002t0001g0195a0002c0002t0001g0196others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413-4128A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020453 | ||||||
chrX:20020477 | TC | T | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-4153delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020477 | ||||||
chrX:20020585 | C | A | 1 | a0002c0002t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1413-4260G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020585 | ||||||
chrX:20020614 | TC | T | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-4290delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020614 | ||||||
chrX:20020808 | C | G | 87 | a0001c0001t0001g0087a0002c0002t0001g0001a0002c0002t0001g0125others(84): Show | 88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1412+4143G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020808 | ||||||
chrX:20020812 | C | T | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412+4139G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020812 | ||||||
chrX:20020932 | T | TC | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1412+4018dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020932 | ||||||
chrX:20020962 | T | C | 2 | a0002c0002t0001g0154a0002c0002t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1412+3989A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020962 | ||||||
chrX:20021841 | G | A | 7 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412+3110C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20021841 | ||||||
chrX:20022640 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1412+2311T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022640 | ||||||
chrX:20022793 | A | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+2158T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022793 | ||||||
chrX:20022914 | A | G | 1 | a0002c0003t0001g0017 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1412+2037T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022914 | ||||||
chrX:20023142 | C | A | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+1809G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023142 | ||||||
chrX:20023452 | G | A | 8 | a0002c0002t0001g0178a0002c0002t0001g0179a0002c0002t0001g0180others(5): Show | 8 | HG01081.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412+1499C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023452 | ||||||
chrX:20023527 | G | A | 4 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0122others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412+1424C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023527 | ||||||
chrX:20023578 | T | A | 95 | a0001c0001t0001g0087a0002c0002t0001g0001a0002c0002t0001g0125others(92): Show | 96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.1412+1373A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023578 | ||||||
chrX:20023601 | C | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+1350G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023601 | ||||||
chrX:20023937 | C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0067 | 2 | NA18948.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1412+1014G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023937 | ||||||
chrX:20024186 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1412+764dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024186 | ||||||
chrX:20024329 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1412+621dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024329 | ||||||
chrX:20024344 | C | T | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412+607G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024344 | ||||||
chrX:20024367 | A | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412+584T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024367 | ||||||
chrX:20024481 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1412+470C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024481 | ||||||
chrX:20024729 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1412+221dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024729 | ||||||
chrX:20024842 | A | G | 3 | a0001c0001t0001g0065a0006c0008t0001g0061a0009c0009t0001g0020 | 3 | HG02074.hp1 NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1412+109T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024842 | ||||||
chrX:20025171 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280-89dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025171 | ||||||
chrX:20025201 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280-119dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025201 | ||||||
chrX:20025295 | T | C | 5 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-212A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025295 | ||||||
chrX:20025349 | T | A | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-266A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025349 | ||||||
chrX:20025389 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1279+292T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025389 | ||||||
chrX:20025423 | A | G | 12 | a0002c0002t0001g0176a0002c0002t0001g0189a0002c0002t0001g0205others(9): Show | 12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279+258T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025423 | ||||||
chrX:20025429 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1279+251dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025429 | ||||||
chrX:20025581 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1279+99dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025581 | ||||||
chrX:20025644 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1279+37G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025644 | ||||||
chrX:20025961 | C | A | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1008-9G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20025961 | ||||||
chrX:20025990 | G | GC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-39dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20025990 | ||||||
chrX:20026075 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1008-123G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026075 | ||||||
chrX:20026186 | T | C | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1008-234A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026186 | ||||||
chrX:20026609 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-658dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026609 | ||||||
chrX:20026635 | A | AG | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-684dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026635 | ||||||
chrX:20026674 | A | AG | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-723dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026674 | ||||||
chrX:20026689 | G | A | 26 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(23): Show | 26 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1008-737C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026689 | ||||||
chrX:20026697 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1008-745T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026697 | ||||||
chrX:20026747 | A | AG | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-796dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026747 | ||||||
chrX:20026760 | C | CT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-809dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026760 | ||||||
chrX:20026888 | T | C | 2 | a0002c0002t0001g0154a0002c0002t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1008-936A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026888 | ||||||
chrX:20027058 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1008-1106A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027058 | ||||||
chrX:20027064 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-1113dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027064 | ||||||
chrX:20027196 | C | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-1244G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027196 | ||||||
chrX:20027242 | C | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0089 | 2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1008-1290G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027242 | ||||||
chrX:20027329 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-1378dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027329 | ||||||
chrX:20027473 | T | TG | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-1522dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027473 | ||||||
chrX:20027752 | C | CG | 1 | a0001c0001t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1008-1801dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027752 | ||||||
chrX:20027757 | G | GGA | 12 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0036others(9): Show | 12 | HG02615.hp1 HG02630.hp2 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.1008-1807_1008-180 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027757 | G | GGAGA | 3 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0005g0070 | 3 | HG01123.hp2 NA18943.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1008-1809_1008-180 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027757 | G | GGAGAGA | 1 | a0001c0001t0001g0011 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1008-1811_1008-180 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027757 | GGA | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0114others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008-1807_1008-180 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027757 | GGAGA | G | 9 | a0001c0001t0001g0087a0002c0002t0001g0125a0002c0002t0001g0145others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008-1809_1008-180 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027757 | GGAGAGA | G | 56 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(53): Show | 56 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1008-1811_1008-180 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | ||||||
chrX:20027758 | GAGA | G | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1008-1809_1008-180 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027758 | ||||||
chrX:20027758 | GAGAGA | G | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-1811_1008-180 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027758 | ||||||
chrX:20027763 | A | G | 4 | a0002c0002t0001g0176a0002c0005t0001g0121a0002c0005t0001g0122others(1): Show | 4 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-1811T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027763 | ||||||
chrX:20027765 | A | G | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-1813T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027765 | ||||||
chrX:20027786 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1008-1834C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027786 | ||||||
chrX:20027790 | GAC | G | 4 | a0002c0004t0001g0173a0002c0004t0001g0174a0002c0004t0001g0202others(1): Show | 4 | HG01106.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-1840_1008-183 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027790 | ||||||
chrX:20027792 | C | G | 3 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0206 | 3 | HG02630.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-1840G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027792 | ||||||
chrX:20027882 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-1931dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027882 | ||||||
chrX:20028183 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-2232dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20028183 | ||||||
chrX:20028777 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-2826dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20028777 | ||||||
chrX:20028845 | A | AG | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-2894dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20028845 | ||||||
chrX:20028936 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-2984A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20028936 | ||||||
chrX:20029005 | C | T | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008-3053G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029005 | ||||||
chrX:20029185 | G | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-3233C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029185 | ||||||
chrX:20029197 | A | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-3245T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029197 | ||||||
chrX:20029250 | G | T | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-3298C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029250 | ||||||
chrX:20029669 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-3718dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029669 | ||||||
chrX:20029680 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-3729dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029680 | ||||||
chrX:20029684 | C | T | 2 | a0001c0001t0001g0043a0002c0002t0001g0205 | 2 | HG02886.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1008-3732G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029684 | ||||||
chrX:20029786 | T | C | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-3834A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029786 | ||||||
chrX:20029789 | A | AT | 102 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(99): Show | 103 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.1008-3838dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029789 | ||||||
chrX:20029789 | A | ATT | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-3839_1008-383 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029789 | ||||||
chrX:20029789 | AT | A | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1008-3838delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029789 | ||||||
chrX:20029829 | T | TA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-3878dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029829 | ||||||
chrX:20029960 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-4009dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029960 | ||||||
chrX:20030050 | C | T | 8 | a0002c0002t0001g0178a0002c0002t0001g0179a0002c0002t0001g0180others(5): Show | 8 | HG01081.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-4098G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030050 | ||||||
chrX:20030252 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-4301dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030252 | ||||||
chrX:20030541 | G | GT | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-4590dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030541 | ||||||
chrX:20030829 | T | C | 90 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(87): Show | 91 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.1008-4877A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030829 | ||||||
chrX:20030847 | T | C | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-4895A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030847 | ||||||
chrX:20031062 | G | A | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-5110C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031062 | ||||||
chrX:20031118 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1008-5166C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031118 | ||||||
chrX:20031134 | C | CA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-5183dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031134 | ||||||
chrX:20031214 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1008-5262G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031214 | ||||||
chrX:20031215 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1008-5263C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031215 | ||||||
chrX:20031291 | A | AAAAAT | 2 | a0002c0002t0001g0126a0002c0002t0001g0177 | 2 | HG00733.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1008-5344_1008-534 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | A | AAAAATAA others(3): Show |
1 | a0002c0002t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1008-5349_1008-534 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0106 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1008-5354_1008-534 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | AAAAAT | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1008-5344_1008-534 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | AAAAATAA others(3): Show |
A | 8 | a0002c0002t0001g0189a0002c0002t0002g0186a0002c0002t0002g0204others(5): Show | 8 | HG01106.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-5349_1008-534 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | AAAAATAA others(8): Show |
A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-5354_1008-534 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031291 | AAAAATAA others(13): Show |
A | 2 | a0001c0001t0001g0076a0002c0002t0001g0149 | 2 | HG01258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1008-5359_1008-534 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | ||||||
chrX:20031453 | G | GA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-5502dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031453 | ||||||
chrX:20031526 | A | G | 12 | a0002c0002t0001g0176a0002c0002t0001g0189a0002c0002t0001g0205others(9): Show | 12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1008-5574T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031526 | ||||||
chrX:20031533 | G | A | 84 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(81): Show | 85 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1008-5581C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031533 | ||||||
chrX:20031766 | C | CA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-5815dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031766 | ||||||
chrX:20032357 | G | C | 11 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0004t0001g0172others(8): Show | 11 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008-6405C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20032357 | ||||||
chrX:20032843 | T | TC | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1008-6892dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20032843 | ||||||
chrX:20033238 | TG | T | 1 | a0002c0002t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1008-7287delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033238 | ||||||
chrX:20033502 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0042others(2): Show | 5 | HG00280.hp1 HG01496.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-7550G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033502 | ||||||
chrX:20033688 | C | T | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1008-7736G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033688 | ||||||
chrX:20033759 | G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | NA18979.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1008-7807C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033759 | ||||||
chrX:20034068 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1008-8116A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034068 | ||||||
chrX:20034225 | C | CA | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0098others(2): Show | 5 | HG01261.hp1 HG02257.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-8274dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | ||||||
chrX:20034225 | CA | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1008-8274delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | ||||||
chrX:20034225 | CAA | C | 61 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(58): Show | 62 | HG00609.hp1 HG00735.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.1007+8275_1008-827 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | ||||||
chrX:20034225 | CAAA | C | 12 | a0002c0002t0001g0166a0002c0002t0001g0168a0002c0002t0001g0177others(9): Show | 12 | HG00733.hp1 HG01081.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1007+8274_1008-827 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | ||||||
chrX:20034372 | G | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1007+8130C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034372 | ||||||
chrX:20034457 | C | T | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1007+8045G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034457 | ||||||
chrX:20034564 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1007+7938A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034564 | ||||||
chrX:20034586 | G | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+7916C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034586 | ||||||
chrX:20034934 | C | T | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+7568G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034934 | ||||||
chrX:20034969 | A | G | 7 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+7533T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034969 | ||||||
chrX:20035162 | G | A | 1 | a0002c0002t0001g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1007+7340C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035162 | ||||||
chrX:20035492 | A | T | 2 | a0002c0002t0001g0154a0002c0002t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1007+7010T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035492 | ||||||
chrX:20035861 | C | T | 71 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007+6641G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035861 | ||||||
chrX:20035887 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1007+6615A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035887 | ||||||
chrX:20035912 | CAA | C | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1007+6588_1007+658 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035912 | ||||||
chrX:20035926 | A | ATG | 2 | a0002c0002t0001g0132a0003c0016t0009g0208 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1007+6574_1007+657 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | ||||||
chrX:20035926 | ATG | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(98): Show | 101 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.1007+6574_1007+657 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | ||||||
chrX:20035926 | ATGTG | A | 9 | a0002c0002t0001g0152a0002c0002t0001g0178a0002c0002t0001g0179others(6): Show | 9 | HG01081.hp1 HG01361.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007+6572_1007+657 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | ||||||
chrX:20035926 | ATGTGTG | A | 64 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(61): Show | 64 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1007+6570_1007+657 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | ||||||
chrX:20035928 | G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0054others(2): Show | 5 | HG03486.hp1 NA18943.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+6574C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035928 | ||||||
chrX:20036144 | C | T | 8 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(5): Show | 8 | HG01070.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+6358G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036144 | ||||||
chrX:20036178 | C | T | 76 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(73): Show | 76 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1007+6324G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036178 | ||||||
chrX:20036306 | G | A | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007+6196C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036306 | ||||||
chrX:20036418 | A | AT | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1007+6083dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036418 | ||||||
chrX:20036532 | G | A | 71 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(68): Show | 71 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007+5970C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036532 | ||||||
chrX:20036609 | TA | T | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1007+5892delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036609 | ||||||
chrX:20036740 | C | T | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+5762G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036740 | ||||||
chrX:20036866 | T | G | 1 | a0001c0001t0001g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1007+5636A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036866 | ||||||
chrX:20036903 | C | CA | 2 | a0001c0001t0001g0073a0001c0001t0001g0099 | 2 | HG02027.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1007+5598dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | ||||||
chrX:20036903 | CA | C | 76 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0053others(73): Show | 77 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1007+5598delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | ||||||
chrX:20036903 | CAA | C | 3 | a0002c0002t0001g0130a0002c0002t0001g0168a0003c0016t0009g0208 | 3 | HG01070.hp1 HG06807.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1007+5597_1007+559 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | ||||||
chrX:20036903 | CAAA | C | 1 | a0002c0005t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1007+5596_1007+559 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | ||||||
chrX:20036903 | CAAAA | C | 2 | a0002c0002t0001g0176a0002c0005t0001g0122 | 2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1007+5595_1007+559 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | ||||||
chrX:20037295 | G | A | 91 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(88): Show | 92 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1007+5207C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037295 | ||||||
chrX:20037805 | G | A | 1 | a0002c0004t0001g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1007+4697C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037805 | ||||||
chrX:20037807 | C | T | 89 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(86): Show | 90 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1007+4695G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037807 | ||||||
chrX:20038221 | C | G | 3 | a0002c0002t0001g0158a0002c0002t0001g0167a0002c0002t0001g0193 | 3 | HG01123.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1007+4281G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038221 | ||||||
chrX:20038399 | T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0013t0001g0190 | 3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1007+4103A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038399 | ||||||
chrX:20038559 | C | T | 89 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(86): Show | 90 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1007+3943G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038559 | ||||||
chrX:20038573 | G | A | 1 | a0002c0014t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1007+3929C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038573 | ||||||
chrX:20038991 | C | T | 5 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(2): Show | 5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+3511G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038991 | ||||||
chrX:20038999 | G | A | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+3503C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038999 | ||||||
chrX:20039001 | G | T | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+3501C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039001 | ||||||
chrX:20039204 | C | A | 92 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(89): Show | 93 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1007+3298G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039204 | ||||||
chrX:20039236 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1007+3266T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039236 | ||||||
chrX:20039249 | G | A | 1 | a0002c0002t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1007+3253C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039249 | ||||||
chrX:20039979 | C | A | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1007+2523G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039979 | ||||||
chrX:20039997 | C | CA | 40 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0024others(37): Show | 40 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1007+2504dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039997 | ||||||
chrX:20039997 | C | CAA | 2 | a0002c0002t0001g0145a0002c0002t0001g0164 | 2 | HG02055.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1007+2503_1007+250 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039997 | ||||||
chrX:20039997 | CA | C | 3 | a0002c0002t0001g0175a0002c0002t0001g0179a0002c0002t0002g0139 | 3 | HG01070.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1007+2504delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039997 | ||||||
chrX:20040108 | C | T | 97 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(94): Show | 98 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.1007+2394G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040108 | ||||||
chrX:20040496 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1007+2006G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040496 | ||||||
chrX:20040549 | C | T | 3 | a0002c0002t0001g0125a0002c0002t0001g0145a0002c0002t0001g0170 | 3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1007+1953G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040549 | ||||||
chrX:20040577 | C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1007+1925G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040577 | ||||||
chrX:20040641 | A | G | 99 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(96): Show | 100 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.1007+1861T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040641 | ||||||
chrX:20040719 | G | A | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1007+1783C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040719 | ||||||
chrX:20040864 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1007+1638G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040864 | ||||||
chrX:20040949 | C | A | 1 | a0002c0003t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1007+1553G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040949 | ||||||
chrX:20041189 | G | A | 1 | a0002c0002t0001g0182 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1007+1313C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041189 | ||||||
chrX:20041516 | A | C | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1007+986T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041516 | ||||||
chrX:20041900 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1007+602A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041900 | ||||||
chrX:20042307 | T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0056 | 2 | NA18953.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1007+195A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20042307 | ||||||
chrX:20042402 | G | A | 5 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(2): Show | 5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+100C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20042402 | ||||||
chrX:20042895 | G | A | 12 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(9): Show | 12 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-266C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042895 | ||||||
chrX:20042940 | C | G | 44 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(41): Show | 44 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.880-311G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042940 | ||||||
chrX:20042952 | A | G | 5 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-323T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042952 | ||||||
chrX:20043153 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.880-524T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043153 | ||||||
chrX:20043263 | G | A | 1 | a0002c0002t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.880-634C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043263 | ||||||
chrX:20043376 | CCTCTT | C | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-752_880-748del others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043376 | ||||||
chrX:20043464 | T | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-835A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043464 | ||||||
chrX:20043685 | T | A | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+679A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043685 | ||||||
chrX:20043696 | A | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+668T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043696 | ||||||
chrX:20043886 | T | C | 1 | a0002c0002t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.879+478A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043886 | ||||||
chrX:20044131 | T | G | 2 | a0002c0002t0001g0144a0002c0002t0001g0149 | 2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.879+233A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20044131 | ||||||
chrX:20044757 | T | C | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.719-233A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20044757 | ||||||
chrX:20045293 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.719-769C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045293 | ||||||
chrX:20045526 | C | CG | 5 | a0001c0001t0001g0053a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-1003dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045526 | ||||||
chrX:20045527 | G | GA | 8 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0056others(5): Show | 8 | HG02027.hp1 HG03098.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.719-1004dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | ||||||
chrX:20045527 | GA | G | 65 | a0001c0001t0001g0085a0002c0002t0001g0001a0002c0002t0001g0125others(62): Show | 66 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.719-1004delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | ||||||
chrX:20045527 | GAA | G | 10 | a0002c0002t0001g0126a0002c0002t0001g0169a0002c0002t0001g0179others(7): Show | 10 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.719-1005_719-1004d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | ||||||
chrX:20045528 | A | G | 1 | a0002c0002t0001g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.719-1004T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045528 | ||||||
chrX:20045574 | C | A | 2 | a0001c0001t0001g0086a0004c0011t0006g0004 | 2 | HG01928.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.719-1050G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045574 | ||||||
chrX:20046283 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.719-1759C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046283 | ||||||
chrX:20046504 | G | A | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1980C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046504 | ||||||
chrX:20046539 | T | C | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.719-2015A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046539 | ||||||
chrX:20047214 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.719-2690A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047214 | ||||||
chrX:20047239 | A | C | 1 | a0002c0002t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.719-2715T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047239 | ||||||
chrX:20047240 | C | G | 1 | a0002c0002t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.719-2716G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047240 | ||||||
chrX:20047449 | T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0046others(7): Show | 10 | HG00642.hp1 HG01261.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.719-2925A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047449 | ||||||
chrX:20047648 | C | CA | 2 | a0001c0001t0001g0035a0002c0005t0001g0121 | 2 | HG01256.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.719-3125dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047648 | ||||||
chrX:20047648 | CA | C | 65 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0127others(62): Show | 66 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.719-3125delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047648 | ||||||
chrX:20047649 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.719-3125T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047649 | ||||||
chrX:20047873 | G | A | 6 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+2951C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047873 | ||||||
chrX:20047875 | GA | G | 82 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(79): Show | 83 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.718+2948delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047875 | ||||||
chrX:20047932 | A | G | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+2892T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047932 | ||||||
chrX:20048138 | G | T | 88 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(85): Show | 89 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.718+2686C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048138 | ||||||
chrX:20048459 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.718+2365C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048459 | ||||||
chrX:20048521 | C | T | 1 | a0002c0002t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.718+2303G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048521 | ||||||
chrX:20048884 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.718+1940A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048884 | ||||||
chrX:20048929 | ATATACAT others(15): Show |
A | 1 | a0002c0002t0001g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+1873_718+1894d others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048929 | ||||||
chrX:20048934 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.718+1866_718+1889d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048934 | ||||||
chrX:20048945 | A | ATATATGT others(5): Show |
1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718+1867_718+1878d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048945 | ||||||
chrX:20049270 | A | AT | 2 | a0001c0001t0001g0002a0001c0001t0001g0102 | 2 | NA18940.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.718+1553dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049270 | ||||||
chrX:20049270 | AT | A | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.718+1553delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049270 | ||||||
chrX:20049270 | ATT | A | 94 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(91): Show | 95 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.718+1552_718+1553d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049270 | ||||||
chrX:20049270 | ATTT | A | 1 | a0002c0002t0002g0124 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718+1551_718+1553d others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049270 | ||||||
chrX:20049640 | G | C | 1 | a0002c0002t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.718+1184C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049640 | ||||||
chrX:20049761 | T | C | 95 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(92): Show | 96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.718+1063A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049761 | ||||||
chrX:20049871 | A | C | 5 | a0002c0002t0001g0185a0002c0002t0002g0124a0002c0002t0002g0139others(2): Show | 5 | HG01070.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+953T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049871 | ||||||
chrX:20049916 | T | A | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+908A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049916 | ||||||
chrX:20050691 | G | A | 2 | a0002c0002t0001g0147a0002c0002t0001g0192 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.718+133C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20050691 | ||||||
chrX:20051556 | C | CA | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-611dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20051556 | ||||||
chrX:20051560 | C | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-614G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20051560 | ||||||
chrX:20051560 | C | CA | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.596-615dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20051560 | ||||||
chrX:20052706 | G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0013t0001g0190 | 3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.595+172C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20052706 | ||||||
chrX:20053200 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485-212T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053200 | ||||||
chrX:20053277 | C | T | 9 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0136others(6): Show | 9 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-289G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053277 | ||||||
chrX:20053309 | T | A | 18 | a0002c0002t0001g0143a0002c0002t0001g0177a0002c0002t0001g0178others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-321A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053309 | ||||||
chrX:20053809 | G | A | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485-821C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053809 | ||||||
chrX:20053902 | G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0100 | 2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.485-914C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053902 | ||||||
chrX:20053912 | C | T | 2 | a0002c0002t0001g0154a0002c0002t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485-924G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053912 | ||||||
chrX:20054093 | C | T | 2 | a0002c0002t0001g0184a0002c0003t0001g0014 | 2 | HG01361.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.485-1105G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054093 | ||||||
chrX:20054210 | A | C | 1 | a0002c0004t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.485-1222T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054210 | ||||||
chrX:20054228 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.485-1240C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054228 | ||||||
chrX:20054281 | T | A | 95 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(92): Show | 96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.485-1293A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054281 | ||||||
chrX:20054286 | C | T | 78 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(75): Show | 79 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.485-1298G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054286 | ||||||
chrX:20054325 | T | A | 2 | a0002c0002t0001g0151a0002c0002t0001g0166 | 2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.485-1337A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054325 | ||||||
chrX:20054499 | T | C | 7 | a0002c0002t0001g0171a0002c0002t0001g0184a0002c0002t0001g0188others(4): Show | 7 | HG01361.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-1511A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054499 | ||||||
chrX:20054594 | C | CT | 1 | a0002c0002t0001g0164 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.485-1607dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054594 | ||||||
chrX:20054771 | G | A | 3 | a0002c0002t0001g0125a0002c0002t0001g0145a0002c0002t0001g0170 | 3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.485-1783C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054771 | ||||||
chrX:20055076 | C | CT | 1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.484+1603dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055076 | ||||||
chrX:20055076 | CT | C | 69 | a0001c0001t0001g0053a0002c0002t0001g0125a0002c0002t0001g0126others(66): Show | 69 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.484+1603delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055076 | ||||||
chrX:20055436 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.484+1244C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055436 | ||||||
chrX:20055623 | G | C | 1 | a0002c0003t0001g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.484+1057C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055623 | ||||||
chrX:20056167 | C | T | 92 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(89): Show | 93 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.484+513G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056167 | ||||||
chrX:20056323 | C | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(76): Show | 80 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.484+357G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056323 | ||||||
chrX:20056343 | C | A | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.484+337G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056343 | ||||||
chrX:20056416 | A | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+264T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056416 | ||||||
chrX:20056482 | A | T | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+198T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056482 | ||||||
chrX:20056626 | T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0054 | 2 | NA18960.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.484+54A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056626 | ||||||
chrX:20057010 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.373-219G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057010 | ||||||
chrX:20057392 | C | T | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-601G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057392 | ||||||
chrX:20057500 | G | C | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.373-709C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057500 | ||||||
chrX:20057590 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.373-799C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057590 | ||||||
chrX:20057612 | C | T | 40 | a0002c0002t0001g0127a0002c0002t0001g0142a0002c0002t0001g0144others(37): Show | 40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-821G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057612 | ||||||
chrX:20058171 | G | A | 11 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(8): Show | 11 | HG00733.hp1 HG01081.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.373-1380C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058171 | ||||||
chrX:20058668 | C | A | 1 | a0002c0002t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373-1877G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058668 | ||||||
chrX:20058913 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.373-2122G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058913 | ||||||
chrX:20058953 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.373-2162T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058953 | ||||||
chrX:20059199 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.373-2408A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059199 | ||||||
chrX:20059308 | T | C | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2517A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059308 | ||||||
chrX:20059522 | T | TG | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.373-2732dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059522 | ||||||
chrX:20059572 | A | AG | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.373-2782dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059572 | ||||||
chrX:20059589 | T | TGGAA | 20 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0032others(17): Show | 20 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.373-2802_373-2799d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | T | TGGAAGGA others(1): Show |
5 | a0002c0002t0001g0125a0002c0002t0001g0143a0002c0002t0001g0145others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2806_373-2799d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | T | TGGAAGGA others(5): Show |
29 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(26): Show | 29 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.373-2810_373-2799d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | T | TGGAAGGA others(9): Show |
9 | a0002c0002t0001g0127a0002c0002t0001g0141a0002c0002t0001g0142others(6): Show | 9 | HG00733.hp1 HG01081.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-2814_373-2799d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | T | TGGAAGGA others(13): Show |
4 | a0002c0002t0001g0152a0002c0002t0001g0159a0002c0002t0001g0160others(1): Show | 4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2818_373-2799d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | TGGAA | T | 6 | a0001c0001t0001g0047a0001c0001t0001g0091a0001c0001t0001g0119others(3): Show | 6 | HG03041.hp1 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-2802_373-2799d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059589 | TGGAAGGA others(1): Show |
T | 14 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0059others(11): Show | 14 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-2806_373-2799d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | ||||||
chrX:20059620 | A | G | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2829T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059620 | ||||||
chrX:20059621 | A | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2830T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059621 | ||||||
chrX:20059625 | AGGGT | A | 4 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0122others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2838_373-2835d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059625 | ||||||
chrX:20059628 | G | A | 6 | a0002c0002t0001g0163a0002c0002t0001g0164a0002c0002t0001g0167others(3): Show | 6 | HG01192.hp1 HG01256.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-2837C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059628 | ||||||
chrX:20059629 | T | A | 6 | a0002c0002t0001g0163a0002c0002t0001g0164a0002c0002t0001g0167others(3): Show | 6 | HG01192.hp1 HG01256.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-2838A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | ||||||
chrX:20059629 | T | TGGAA | 3 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0088 | 3 | NA18943.hp1 NA18944.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.373-2842_373-2839d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | ||||||
chrX:20059629 | TGGAA | T | 1 | a0002c0002t0001g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.373-2842_373-2839d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | ||||||
chrX:20059629 | TGGAAGGA others(5): Show |
T | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-2850_373-2839d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | ||||||
chrX:20059633 | A | AGGAAGGG others(1): Show |
1 | a0002c0002t0001g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.373-2843_373-2842i others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059633 | ||||||
chrX:20059637 | A | AGGGT | 4 | a0002c0002t0001g0163a0002c0002t0001g0164a0002c0002t0001g0168others(1): Show | 4 | NA18965.hp1 NA18979.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2847_373-2846i others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059637 | ||||||
chrX:20059677 | AAGAC | A | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.373-2890_373-2887d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059677 | ||||||
chrX:20059681 | C | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2890G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059681 | ||||||
chrX:20059736 | AGAAGGAA others(10): Show |
A | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-2962_373-2946d others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059736 | ||||||
chrX:20059950 | C | T | 1 | a0002c0003t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.373-3159G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059950 | ||||||
chrX:20059995 | T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0032others(2): Show | 5 | NA18971.hp1 NA18984.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-3204A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059995 | ||||||
chrX:20060012 | T | C | 1 | a0002c0002t0001g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.373-3221A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060012 | ||||||
chrX:20060023 | C | CT | 1 | a0002c0003t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.373-3233dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060023 | ||||||
chrX:20060378 | G | A | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.372+3036C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060378 | ||||||
chrX:20060411 | AAGAAAAG | A | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.372+2996_372+3002d others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060411 | ||||||
chrX:20060414 | AAAAGAG | A | 1 | a0002c0004t0001g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.372+2994_372+2999d others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060414 | ||||||
chrX:20060415 | AAAG | A | 1 | a0001c0001t0001g0119 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.372+2996_372+2998d others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060415 | ||||||
chrX:20060416 | AAGAG | A | 13 | a0001c0001t0001g0114a0002c0002t0001g0129a0002c0002t0001g0136others(10): Show | 13 | HG01070.hp2 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.372+2994_372+2997d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060416 | ||||||
chrX:20060428 | G | GAGA | 1 | a0002c0002t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.372+2983_372+2985d others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | G | GAGAA | 6 | a0002c0002t0001g0134a0002c0002t0001g0141a0002c0002t0001g0142others(3): Show | 6 | HG01081.hp2 HG02572.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+2985_372+2986i others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | G | GAGAAAGA others(1): Show |
2 | a0002c0002t0001g0137a0003c0016t0009g0208 | 2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.372+2985_372+2986i others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | GAGAGAGA others(1): Show |
G | 24 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0127others(21): Show | 25 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.372+2978_372+2985d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | GAGAGAGA others(5): Show |
G | 11 | a0002c0002t0001g0126a0002c0002t0001g0155a0002c0002t0001g0158others(8): Show | 11 | HG01167.hp1 HG01192.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.372+2974_372+2985d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | GAGAGAGA others(9): Show |
G | 5 | a0002c0002t0001g0146a0002c0002t0001g0154a0002c0002t0001g0169others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+2970_372+2985d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | GAGAGAGA others(13): Show |
G | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.372+2966_372+2985d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060428 | GAGAGAGA others(17): Show |
G | 5 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0148others(2): Show | 5 | HG02257.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+2962_372+2985d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | ||||||
chrX:20060431 | AG | A | 1 | a0002c0003t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.372+2982delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060431 | ||||||
chrX:20060432 | G | A | 25 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0137others(22): Show | 25 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.372+2982C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | G | GAGAA | 3 | a0001c0001t0001g0065a0001c0001t0001g0076a0002c0003t0001g0015 | 3 | HG01258.hp1 HG02074.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.372+2978_372+2981d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAA | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(31): Show | 34 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.372+2978_372+2981d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAAAGA others(1): Show |
G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(48): Show | 51 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.372+2974_372+2981d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAAAGA others(5): Show |
G | 20 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0025others(17): Show | 20 | HG00609.hp1 HG00673.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.372+2970_372+2981d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAAAGA others(9): Show |
G | 3 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0115 | 3 | HG01433.hp1 HG03239.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.372+2966_372+2981d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAAAGA others(13): Show |
G | 2 | a0001c0001t0001g0048a0001c0001t0001g0084 | 2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.372+2962_372+2981d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060432 | GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.372+2958_372+2981d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | ||||||
chrX:20060434 | GAAAGAA | G | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.372+2974_372+2979d others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060434 | ||||||
chrX:20060436 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.372+2978T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060436 | ||||||
chrX:20060448 | A | G | 3 | a0002c0003t0003g0094a0002c0003t0003g0095a0002c0003t0003g0096 | 3 | HG02015.hp1 HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.372+2966T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060448 | ||||||
chrX:20060482 | GAAAGAA | G | 1 | a0002c0002t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372+2926_372+2931d others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060482 | ||||||
chrX:20061118 | C | CA | 9 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0025others(6): Show | 9 | HG01361.hp2 HG02135.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+2295dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | ||||||
chrX:20061118 | CA | C | 60 | a0001c0001t0001g0005a0002c0002t0001g0125a0002c0002t0001g0127others(57): Show | 60 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.372+2295delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | ||||||
chrX:20061118 | CAA | C | 26 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(23): Show | 27 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.372+2294_372+2295d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | ||||||
chrX:20061312 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.372+2102C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061312 | ||||||
chrX:20061709 | C | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1705G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061709 | ||||||
chrX:20061774 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.372+1640A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061774 | ||||||
chrX:20062147 | A | G | 45 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0142others(42): Show | 45 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.372+1267T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062147 | ||||||
chrX:20062404 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.372+1010C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062404 | ||||||
chrX:20062481 | TA | T | 1 | a0002c0002t0001g0164 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.372+932delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062481 | ||||||
chrX:20062746 | A | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+668T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062746 | ||||||
chrX:20063010 | C | T | 93 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(90): Show | 94 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.372+404G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063010 | ||||||
chrX:20063029 | C | CT | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.372+384dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063029 | ||||||
chrX:20063111 | T | C | 1 | a0002c0003t0001g0017 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.372+303A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063111 | ||||||
chrX:20063295 | CCAAG | C | 2 | a0002c0002t0001g0147a0002c0002t0001g0192 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.372+115_372+118del others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063295 | ||||||
chrX:20063649 | A | C | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-72T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063649 | ||||||
chrX:20063786 | T | TC | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.209-210dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063786 | ||||||
chrX:20063809 | G | T | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-232C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063809 | ||||||
chrX:20063946 | A | G | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-369T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063946 | ||||||
chrX:20064039 | CA | C | 15 | a0002c0002t0001g0143a0002c0002t0001g0177a0002c0002t0001g0178others(12): Show | 15 | HG00733.hp1 HG01081.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-463delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064039 | ||||||
chrX:20064344 | T | C | 24 | a0002c0002t0001g0143a0002c0002t0001g0171a0002c0002t0001g0177others(21): Show | 24 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.208+384A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064344 | ||||||
chrX:20064363 | C | A | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.208+365G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064363 | ||||||
chrX:20064436 | G | A | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+292C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064436 | ||||||
chrX:20064471 | T | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+257A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064471 | ||||||
chrX:20064659 | G | A | 9 | a0002c0002t0001g0144a0002c0002t0001g0148a0002c0002t0001g0149others(6): Show | 9 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+69C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064659 | ||||||
chrX:20064887 | A | AC | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.131-83dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20064887 | ||||||
chrX:20064905 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.131-100C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20064905 | ||||||
chrX:20064993 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.131-188G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20064993 | ||||||
chrX:20065108 | T | C | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-303A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065108 | ||||||
chrX:20065163 | C | G | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-358G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065163 | ||||||
chrX:20065264 | C | CT | 4 | a0001c0001t0001g0031a0001c0001t0001g0079a0002c0002t0001g0199others(1): Show | 4 | HG03209.hp1 HG03486.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-460dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065264 | ||||||
chrX:20065264 | CT | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0071a0002c0002t0001g0166others(2): Show | 5 | HG03017.hp1 NA18957.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-460delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065264 | ||||||
chrX:20065264 | CTTT | C | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-462_131-460del others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065264 | ||||||
chrX:20065321 | CG | C | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.131-517delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065321 | ||||||
chrX:20065451 | G | T | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-646C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065451 | ||||||
chrX:20065621 | A | G | 2 | a0002c0002t0001g0189a0002c0003t0001g0017 | 2 | HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-816T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065621 | ||||||
chrX:20065648 | CA | C | 1 | a0001c0001t0001g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-844delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065648 | ||||||
chrX:20065720 | T | C | 1 | a0002c0005t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.131-915A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065720 | ||||||
chrX:20065913 | C | A | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1108G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065913 | ||||||
chrX:20065917 | CT | C | 86 | a0001c0001t0001g0027a0002c0002t0001g0001a0002c0002t0001g0125others(83): Show | 87 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.131-1113delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065917 | ||||||
chrX:20065921 | T | TG | 1 | a0001c0001t0001g0117 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.131-1117_131-1116i others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065921 | ||||||
chrX:20066076 | C | CA | 1 | a0001c0001t0001g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-1272_131-1271i others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066076 | ||||||
chrX:20066282 | G | A | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1477C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066282 | ||||||
chrX:20066319 | T | G | 1 | a0002c0002t0001g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.131-1514A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066319 | ||||||
chrX:20066365 | G | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0141 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.131-1560C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066365 | ||||||
chrX:20066507 | A | AG | 1 | a0001c0001t0001g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-1703_131-1702i others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066507 | ||||||
chrX:20066578 | T | C | 2 | a0002c0002t0001g0189a0002c0003t0001g0017 | 2 | HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-1773A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066578 | ||||||
chrX:20066625 | G | A | 73 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(70): Show | 74 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.131-1820C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066625 | ||||||
chrX:20066973 | C | G | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-2168G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066973 | ||||||
chrX:20067350 | A | G | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-2545T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067350 | ||||||
chrX:20067397 | C | T | 3 | a0002c0002t0001g0158a0002c0002t0001g0167a0002c0002t0001g0193 | 3 | HG01123.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.131-2592G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067397 | ||||||
chrX:20067466 | A | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0041 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-2661T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067466 | ||||||
chrX:20067554 | G | C | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.131-2749C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067554 | ||||||
chrX:20067646 | A | AT | 2 | a0001c0001t0001g0051a0001c0001t0001g0097 | 2 | NA18747.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.131-2842dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067646 | ||||||
chrX:20067646 | AT | A | 1 | a0001c0001t0001g0009 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.131-2842delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067646 | ||||||
chrX:20067663 | T | G | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-2858A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067663 | ||||||
chrX:20068264 | G | A | 86 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(83): Show | 87 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.131-3459C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20068264 | ||||||
chrX:20069039 | TC | T | 1 | a0001c0001t0001g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-4235delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069039 | ||||||
chrX:20069204 | C | CT | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-4400dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069204 | ||||||
chrX:20069493 | G | T | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-4688C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069493 | ||||||
chrX:20069513 | C | G | 1 | a0002c0002t0001g0177 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.131-4708G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069513 | ||||||
chrX:20069734 | T | TG | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-4930dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069734 | ||||||
chrX:20069745 | A | AG | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-4941dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069745 | ||||||
chrX:20069763 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.131-4958G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069763 | ||||||
chrX:20069774 | A | AT | 3 | a0001c0001t0001g0081a0002c0003t0007g0103a0004c0011t0006g0004 | 3 | HG01943.hp1 HG02145.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.131-4970dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069774 | ||||||
chrX:20069774 | AT | A | 75 | a0001c0001t0001g0115a0002c0002t0001g0125a0002c0002t0001g0126others(72): Show | 75 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.131-4970delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069774 | ||||||
chrX:20069774 | ATT | A | 6 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4971_131-4970d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069774 | ||||||
chrX:20069943 | C | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-5138G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069943 | ||||||
chrX:20070105 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.131-5300G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070105 | ||||||
chrX:20070261 | C | CTTAT | 10 | a0001c0001t0001g0040a0001c0001t0001g0067a0002c0002t0001g0167others(7): Show | 10 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-5460_131-5457d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | ||||||
chrX:20070261 | CTTAT | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0023others(20): Show | 23 | HG01123.hp2 HG01256.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-5460_131-5457d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | ||||||
chrX:20070261 | CTTATTTA others(1): Show |
C | 12 | a0001c0001t0001g0065a0002c0002t0001g0133a0002c0002t0001g0134others(9): Show | 12 | HG01070.hp2 HG02074.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-5464_131-5457d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | ||||||
chrX:20070261 | CTTATTTA others(5): Show |
C | 4 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-5468_131-5457d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | ||||||
chrX:20070261 | CTTATTTA others(9): Show |
C | 6 | a0002c0002t0001g0001a0002c0002t0001g0128a0002c0002t0001g0129others(3): Show | 7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-5472_131-5457d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | ||||||
chrX:20070328 | G | GC | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-5524dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070328 | ||||||
chrX:20070451 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131-5646A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070451 | ||||||
chrX:20070491 | A | T | 2 | a0002c0002t0001g0146a0002c0002t0002g0191 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.131-5686T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070491 | ||||||
chrX:20070870 | T | C | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-6065A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070870 | ||||||
chrX:20071007 | G | A | 2 | a0002c0002t0001g0147a0002c0002t0001g0192 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.131-6202C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071007 | ||||||
chrX:20071137 | G | GT | 1 | a0010c0015t0008g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-6333dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071137 | ||||||
chrX:20071241 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.131-6436G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071241 | ||||||
chrX:20071583 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.131-6778G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071583 | ||||||
chrX:20071784 | GTTTGTTT others(3): Show |
G | 1 | a0001c0001t0001g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.131-6989_131-6980d others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071784 | ||||||
chrX:20072341 | C | G | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-7536G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072341 | ||||||
chrX:20072897 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-8092A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072897 | ||||||
chrX:20072898 | TG | T | 1 | a0001c0001t0001g0012 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.131-8094delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072898 | ||||||
chrX:20072903 | G | A | 7 | a0002c0002t0001g0178a0002c0002t0001g0179a0002c0002t0001g0180others(4): Show | 7 | HG01081.hp1 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-8098C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072903 | ||||||
chrX:20072953 | T | A | 1 | a0002c0002t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.131-8148A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072953 | ||||||
chrX:20073043 | T | TC | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-8239dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073043 | ||||||
chrX:20073388 | G | A | 4 | a0002c0002t0001g0127a0002c0002t0001g0142a0002c0002t0001g0153others(1): Show | 4 | HG00735.hp2 HG01081.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-8583C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073388 | ||||||
chrX:20073532 | C | CT | 6 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-8728dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073532 | ||||||
chrX:20073532 | CT | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0054others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-8728delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073532 | ||||||
chrX:20073768 | C | T | 1 | a0002c0002t0001g0203 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.131-8963G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073768 | ||||||
chrX:20073863 | G | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-9058C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073863 | ||||||
chrX:20074131 | G | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-9326C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074131 | ||||||
chrX:20074135 | C | CA | 4 | a0002c0002t0001g0144a0002c0002t0001g0148a0002c0002t0001g0149others(1): Show | 4 | HG02257.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-9331dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074135 | ||||||
chrX:20074135 | CA | C | 5 | a0002c0002t0001g0159a0002c0002t0001g0175a0002c0002t0002g0124others(2): Show | 5 | HG01515.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-9331delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074135 | ||||||
chrX:20074201 | C | T | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-9396G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074201 | ||||||
chrX:20074778 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.131-9973G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074778 | ||||||
chrX:20074908 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.131-10103G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074908 | ||||||
chrX:20075053 | AAAAC | A | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-10252_131-1024 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075053 | ||||||
chrX:20075195 | G | A | 12 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(9): Show | 13 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-10390C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075195 | ||||||
chrX:20075311 | A | G | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-10506T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075311 | ||||||
chrX:20075701 | C | T | 92 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(89): Show | 93 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.131-10896G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075701 | ||||||
chrX:20075813 | T | C | 1 | a0001c0001t0005g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.131-11008A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075813 | ||||||
chrX:20075961 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.131-11156G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075961 | ||||||
chrX:20076204 | C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0041 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-11399G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076204 | ||||||
chrX:20076701 | C | CA | 2 | a0002c0002t0001g0143a0007c0007t0001g0104 | 2 | NA18974.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.131-11897dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076701 | ||||||
chrX:20076701 | CA | C | 5 | a0002c0002t0001g0152a0002c0002t0001g0176a0002c0002t0001g0205others(2): Show | 5 | HG01256.hp1 HG01981.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-11897delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076701 | ||||||
chrX:20076701 | CAA | C | 2 | a0002c0005t0001g0122a0002c0005t0001g0123 | 2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.131-11898_131-1189 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076701 | ||||||
chrX:20076814 | T | C | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-12009A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076814 | ||||||
chrX:20076997 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.131-12192A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076997 | ||||||
chrX:20077137 | C | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0141a0002c0002t0001g0199others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-12332G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077137 | ||||||
chrX:20077192 | C | T | 88 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(85): Show | 89 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.131-12387G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077192 | ||||||
chrX:20077523 | A | G | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-12718T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077523 | ||||||
chrX:20077533 | G | A | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-12728C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077533 | ||||||
chrX:20077859 | G | T | 8 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-13054C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077859 | ||||||
chrX:20077868 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.131-13063T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077868 | ||||||
chrX:20078187 | G | A | 93 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(90): Show | 94 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.131-13382C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20078187 | ||||||
chrX:20078273 | T | C | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-13468A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20078273 | ||||||
chrX:20079980 | G | A | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131-15175C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20079980 | ||||||
chrX:20080051 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.131-15246G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080051 | ||||||
chrX:20080152 | C | G | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-15347G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080152 | ||||||
chrX:20080187 | T | A | 6 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-15382A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080187 | ||||||
chrX:20080268 | C | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-15463G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080268 | ||||||
chrX:20080540 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.131-15735C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080540 | ||||||
chrX:20080583 | T | A | 1 | a0002c0002t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131-15778A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080583 | ||||||
chrX:20080647 | C | T | 1 | a0002c0002t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.131-15842G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080647 | ||||||
chrX:20081140 | T | C | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-16335A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081140 | ||||||
chrX:20081392 | T | C | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-16587A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081392 | ||||||
chrX:20081639 | T | C | 20 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(17): Show | 21 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-16834A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081639 | ||||||
chrX:20081654 | A | AT | 10 | a0002c0002t0001g0138a0002c0002t0001g0140a0002c0002t0001g0171others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-16850dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081654 | ||||||
chrX:20081654 | A | ATT | 1 | a0002c0003t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.131-16851_131-1685 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081654 | ||||||
chrX:20081654 | AT | A | 1 | a0001c0001t0001g0054 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.131-16850delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081654 | ||||||
chrX:20081871 | A | G | 1 | a0002c0002t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.131-17066T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081871 | ||||||
chrX:20082183 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.131-17378G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082183 | ||||||
chrX:20082288 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.131-17483C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082288 | ||||||
chrX:20082398 | G | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17593C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082398 | ||||||
chrX:20082445 | G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0042others(2): Show | 5 | HG00280.hp1 HG01496.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17640C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082445 | ||||||
chrX:20082501 | C | T | 46 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0142others(43): Show | 46 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.131-17696G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082501 | ||||||
chrX:20082629 | T | C | 6 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-17824A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082629 | ||||||
chrX:20082671 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.131-17866C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082671 | ||||||
chrX:20082697 | C | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17892G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082697 | ||||||
chrX:20082931 | G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 203 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(200): Show |
intron_variant | MODIFIER | c.131-18126C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082931 | ||||||
chrX:20083652 | A | T | 12 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(9): Show | 13 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-18847T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083652 | ||||||
chrX:20083724 | C | T | 68 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0133others(65): Show | 68 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.131-18919G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083724 | ||||||
chrX:20083744 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-18939T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083744 | ||||||
chrX:20083833 | G | A | 4 | a0002c0002t0001g0127a0002c0002t0001g0142a0002c0002t0001g0153others(1): Show | 4 | HG00735.hp2 HG01081.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-19028C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083833 | ||||||
chrX:20083976 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.131-19171C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083976 | ||||||
chrX:20084196 | C | CA | 3 | a0001c0001t0001g0025a0001c0001t0001g0111a0001c0001t0001g0119 | 3 | HG03927.hp1 NA18994.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.131-19392dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084196 | ||||||
chrX:20084196 | CA | C | 83 | a0001c0001t0001g0012a0001c0001t0001g0027a0002c0002t0001g0001others(80): Show | 84 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-19392delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084196 | ||||||
chrX:20084199 | A | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0185a0002c0002t0002g0186 | 3 | HG02717.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.131-19394T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084199 | ||||||
chrX:20084331 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.131-19526G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084331 | ||||||
chrX:20084545 | T | TTCCCTCC others(1): Show |
75 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(72): Show | 76 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.131-19748_131-1974 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084545 | T | TTCCCTCC others(5): Show |
12 | a0001c0001t0001g0018a0001c0001t0001g0068a0002c0002t0001g0176others(9): Show | 12 | HG01106.hp1 HG01256.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-19752_131-1974 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084545 | T | TTCCCTCC others(18): Show |
1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.131-19741_131-1974 others(29): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084545 | T | TTCCCTCC others(9): Show |
95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.131-19756_131-1974 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084545 | T | TTCCCTCC others(13): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(8): Show | 11 | HG01099.hp1 HG01255.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-19741_131-1974 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084545 | T | TTCCCTCC others(17): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0100a0002c0003t0007g0103 | 3 | HG02135.hp1 HG02145.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.131-19741_131-1974 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | ||||||
chrX:20084550 | T | TCCCTCCC others(10): Show |
1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.131-19746_131-1974 others(21): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084550 | ||||||
chrX:20084564 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.131-19759A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084564 | ||||||
chrX:20084788 | C | T | 40 | a0002c0002t0001g0127a0002c0002t0001g0142a0002c0002t0001g0144others(37): Show | 40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.131-19983G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084788 | ||||||
chrX:20084895 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.131-20090A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084895 | ||||||
chrX:20085028 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.131-20223C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085028 | ||||||
chrX:20085057 | C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0073 | 2 | NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.131-20252G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085057 | ||||||
chrX:20085641 | C | T | 87 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(84): Show | 88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.131-20836G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085641 | ||||||
chrX:20085660 | T | C | 15 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.131-20855A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085660 | ||||||
chrX:20085689 | G | C | 2 | a0002c0002t0001g0001a0002c0002t0001g0130 | 3 | HG01070.hp1 HG01071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.131-20884C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085689 | ||||||
chrX:20085948 | G | C | 18 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0171others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-21143C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085948 | ||||||
chrX:20086582 | A | T | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131-21777T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20086582 | ||||||
chrX:20086903 | C | T | 2 | a0002c0002t0001g0185a0002c0002t0002g0186 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.131-22098G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20086903 | ||||||
chrX:20087170 | C | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0041 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-22365G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087170 | ||||||
chrX:20087221 | G | A | 7 | a0002c0002t0001g0189a0002c0004t0001g0172a0002c0004t0001g0173others(4): Show | 7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-22416C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087221 | ||||||
chrX:20087240 | G | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-22435C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087240 | ||||||
chrX:20087277 | T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0084 | 2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.131-22472A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087277 | ||||||
chrX:20087297 | C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0100 | 2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.131-22492G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087297 | ||||||
chrX:20087297 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-22492G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087297 | ||||||
chrX:20087641 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131-22836G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087641 | ||||||
chrX:20087879 | C | CT | 23 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0032others(20): Show | 23 | HG01255.hp1 HG01258.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-23075dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | C | CTT | 3 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0087 | 3 | HG04228.hp1 NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.131-23076_131-2307 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CT | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0069others(10): Show | 13 | HG00733.hp1 HG01081.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-23075delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTT | C | 6 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(3): Show | 7 | HG01071.hp1 HG01891.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-23077_131-2307 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTTT | C | 1 | a0002c0002t0001g0130 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-23078_131-2307 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTTTTT | C | 17 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(14): Show | 17 | HG01070.hp2 HG01496.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.131-23080_131-2307 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTTTTTT | C | 2 | a0001c0001t0001g0054a0002c0002t0003g0156 | 2 | HG04199.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.131-23081_131-2307 others(11): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTTTTTT others(1): Show |
C | 43 | a0001c0001t0001g0018a0002c0002t0001g0125a0002c0002t0001g0127others(40): Show | 43 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.131-23082_131-2307 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20087879 | CTTTTTTT others(2): Show |
C | 2 | a0002c0002t0001g0145a0002c0002t0001g0175 | 2 | HG02055.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-23083_131-2307 others(13): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | ||||||
chrX:20088056 | A | AT | 4 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0079others(1): Show | 4 | HG02071.hp1 HG03688.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-23252dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088056 | ||||||
chrX:20088056 | AT | A | 2 | a0002c0002t0002g0139a0002c0003t0001g0013 | 2 | HG01070.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.131-23252delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088056 | ||||||
chrX:20088260 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131-23455T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088260 | ||||||
chrX:20088295 | C | CT | 2 | a0001c0001t0001g0029a0001c0001t0001g0101 | 2 | HG00673.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.131-23491dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088295 | ||||||
chrX:20088295 | CT | C | 75 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(72): Show | 76 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.131-23491delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088295 | ||||||
chrX:20088364 | A | G | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-23559T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088364 | ||||||
chrX:20088468 | G | GT | 40 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(37): Show | 41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.131-23664dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTT | 23 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0035others(20): Show | 23 | HG00140.hp1 HG01358.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-23665_131-2366 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTT | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(7): Show | 10 | HG01255.hp1 HG02165.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-23666_131-2366 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG02040.hp1 HG02056.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-23667_131-2366 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTT | 2 | a0002c0003t0007g0103a0005c0010t0001g0107 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.131-23668_131-2366 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTTT | 2 | a0001c0001t0001g0109a0002c0002t0001g0128 | 2 | NA18970.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-23669_131-2366 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTTTT | 1 | a0002c0002t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131-23670_131-2366 others(11): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTTTT others(2): Show |
1 | a0002c0003t0001g0017 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.131-23672_131-2366 others(13): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-23674_131-2366 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | G | GTTTTTTT others(8): Show |
1 | a0002c0002t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.131-23678_131-2366 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GT | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0085 | 2 | HG01074.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.131-23664delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0106 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.131-23674_131-2366 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.131-23678_131-2366 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.131-23679_131-2366 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.131-23680_131-2366 others(21): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(11): Show |
G | 6 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(3): Show | 6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23681_131-2366 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088468 | GTTTTTTT others(15): Show |
G | 75 | a0001c0001t0001g0018a0001c0001t0001g0087a0002c0002t0001g0125others(72): Show | 75 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.131-23685_131-2366 others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | ||||||
chrX:20088480 | T | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0083 | 2 | HG01952.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.131-23675A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088480 | ||||||
chrX:20088588 | G | C | 1 | a0002c0002t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131-23783C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088588 | ||||||
chrX:20088655 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131-23850A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088655 | ||||||
chrX:20088732 | A | G | 1 | a0002c0002t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-23927T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088732 | ||||||
chrX:20088986 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.131-24181A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088986 | ||||||
chrX:20089296 | G | T | 87 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(84): Show | 88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.131-24491C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089296 | ||||||
chrX:20089755 | T | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0141a0002c0002t0001g0199others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-24950A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089755 | ||||||
chrX:20089822 | C | A | 1 | a0008c0006t0001g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131-25017G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089822 | ||||||
chrX:20089931 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.131-25126A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089931 | ||||||
chrX:20090278 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.131-25473C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090278 | ||||||
chrX:20090342 | C | T | 7 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-25537G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090342 | ||||||
chrX:20090363 | C | CA | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.131-25559dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | ||||||
chrX:20090363 | CA | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.131-25559delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | ||||||
chrX:20090363 | CAA | C | 12 | a0001c0001t0001g0007a0002c0002t0001g0141a0002c0002t0001g0146others(9): Show | 12 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-25560_131-2555 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | ||||||
chrX:20090363 | CAAA | C | 65 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(62): Show | 66 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.131-25561_131-2555 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | ||||||
chrX:20090363 | CAAAA | C | 11 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(8): Show | 11 | HG01106.hp1 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-25562_131-2555 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | ||||||
chrX:20090954 | G | A | 82 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(79): Show | 83 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.130+25796C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090954 | ||||||
chrX:20090972 | C | CA | 1 | a0002c0004t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+25777dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090972 | ||||||
chrX:20091052 | C | CT | 13 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG01496.hp2 HG01981.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+25697dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091052 | ||||||
chrX:20091052 | CT | C | 1 | a0001c0001t0001g0054 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.130+25697delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091052 | ||||||
chrX:20091199 | G | C | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+25551C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091199 | ||||||
chrX:20091919 | T | C | 14 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+24831A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091919 | ||||||
chrX:20092012 | G | T | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+24738C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092012 | ||||||
chrX:20092118 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+24632A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092118 | ||||||
chrX:20092173 | C | T | 1 | a0001c0001t0005g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130+24577G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092173 | ||||||
chrX:20092222 | C | T | 86 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(83): Show | 87 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.130+24528G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092222 | ||||||
chrX:20092368 | TC | T | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130+24381delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092368 | ||||||
chrX:20092514 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+24236T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092514 | ||||||
chrX:20093419 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.130+23331C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093419 | ||||||
chrX:20093614 | G | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0140 | 2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.130+23136C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093614 | ||||||
chrX:20093619 | T | C | 1 | a0002c0002t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130+23131A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093619 | ||||||
chrX:20093667 | A | G | 4 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0122others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+23083T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093667 | ||||||
chrX:20094073 | C | A | 4 | a0002c0002t0001g0152a0002c0002t0001g0159a0002c0002t0001g0160others(1): Show | 4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+22677G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094073 | ||||||
chrX:20094144 | T | G | 12 | a0002c0002t0001g0176a0002c0002t0001g0189a0002c0002t0001g0205others(9): Show | 12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+22606A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094144 | ||||||
chrX:20094269 | T | C | 4 | a0001c0001t0001g0018a0002c0002t0001g0158a0002c0002t0001g0167others(1): Show | 4 | HG01123.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22481A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094269 | ||||||
chrX:20094479 | AATAC | A | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.130+22267_130+2227 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094479 | ||||||
chrX:20094483 | CATACATA others(65): Show |
C | 2 | a0002c0002t0001g0001a0002c0002t0001g0130 | 3 | HG01070.hp1 HG01071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.130+22195_130+2226 others(76): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094483 | ||||||
chrX:20094487 | CAT | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 25 | HG00280.hp1 HG01243.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.130+22261_130+2226 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | ||||||
chrX:20094487 | CATAT | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0064a0001c0001t0001g0076 | 3 | HG01258.hp1 HG02132.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.130+22259_130+2226 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | ||||||
chrX:20094487 | CATATATA others(1): Show |
C | 1 | a0001c0001t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.130+22255_130+2226 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | ||||||
chrX:20094487 | CATATATA others(23): Show |
C | 1 | a0002c0002t0001g0198 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130+22233_130+2226 others(34): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | ||||||
chrX:20094487 | CATATATA others(87): Show |
C | 2 | a0002c0002t0001g0147a0002c0002t0001g0192 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.130+22169_130+2226 others(98): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | ||||||
chrX:20094488 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0011 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+22234_130+2226 others(32): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094488 | ||||||
chrX:20094490 | A | ATATATAT others(17): Show |
1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130+22259_130+2226 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094490 | ||||||
chrX:20094490 | ATATATAT others(45): Show |
A | 1 | a0002c0002t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+22208_130+2225 others(56): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094490 | ||||||
chrX:20094492 | A | ATATATAT others(15): Show |
1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+22257_130+2225 others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094492 | ||||||
chrX:20094492 | ATATATAT others(43): Show |
A | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+22208_130+2225 others(54): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094492 | ||||||
chrX:20094493 | TATATATA others(69): Show |
T | 1 | a0006c0008t0001g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.130+22181_130+2225 others(80): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094493 | ||||||
chrX:20094494 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0035 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130+22255_130+2225 others(44): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094494 | ||||||
chrX:20094494 | ATATATAT others(41): Show |
A | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+22208_130+2225 others(52): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094494 | ||||||
chrX:20094496 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0086 | 2 | HG01928.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.130+22253_130+2225 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | ||||||
chrX:20094496 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130+22253_130+2225 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | ||||||
chrX:20094496 | ATATATAT others(39): Show |
A | 4 | a0002c0002t0001g0143a0002c0002t0001g0162a0002c0002t0001g0166others(1): Show | 4 | HG01192.hp1 NA19005.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2225 others(50): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | ||||||
chrX:20094498 | ATATATAT others(37): Show |
A | 1 | a0002c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+22208_130+2225 others(48): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094498 | ||||||
chrX:20094500 | ATATATAT others(9): Show |
A | 2 | a0002c0002t0001g0136a0002c0002t0001g0141 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+22234_130+2224 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094500 | ||||||
chrX:20094501 | T | C | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+22249A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094501 | ||||||
chrX:20094502 | ATATATAT others(7): Show |
A | 9 | a0001c0001t0001g0010a0002c0002t0001g0134a0002c0002t0001g0135others(6): Show | 9 | HG01070.hp2 HG02615.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+22234_130+2224 others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094502 | ||||||
chrX:20094502 | ATATATAT others(33): Show |
A | 1 | a0002c0002t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.130+22208_130+2224 others(44): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094502 | ||||||
chrX:20094503 | T | C | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG02165.hp1 HG02165.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+22247A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094503 | ||||||
chrX:20094503 | TATATATA others(59): Show |
T | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+22181_130+2224 others(70): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094503 | ||||||
chrX:20094504 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0137 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+22234_130+2224 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094504 | ||||||
chrX:20094504 | ATATATAT others(31): Show |
A | 7 | a0001c0001t0001g0018a0002c0002t0001g0142a0002c0002t0001g0157others(4): Show | 7 | HG01081.hp2 HG01496.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(42): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094504 | ||||||
chrX:20094505 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.130+22245A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094505 | ||||||
chrX:20094505 | TATATATA others(57): Show |
T | 4 | a0002c0002t0001g0126a0002c0002t0001g0128a0002c0002t0001g0129others(1): Show | 4 | HG01891.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(68): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094505 | ||||||
chrX:20094506 | ATATATAT others(3): Show |
A | 2 | a0002c0002t0001g0133a0002c0002t0002g0204 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.130+22234_130+2224 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094506 | ||||||
chrX:20094506 | ATATATAT others(29): Show |
A | 4 | a0002c0002t0001g0158a0002c0002t0001g0169a0002c0002t0001g0207others(1): Show | 4 | HG01167.hp1 HG03239.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(40): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094506 | ||||||
chrX:20094507 | TATATATA others(55): Show |
T | 5 | a0002c0002t0001g0125a0002c0003t0001g0017a0002c0004t0001g0173others(2): Show | 5 | HG01106.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(66): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094507 | ||||||
chrX:20094508 | ATATATAT others(1): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+22234_130+2224 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094508 | ||||||
chrX:20094508 | ATATATAT others(27): Show |
A | 5 | a0002c0002t0001g0151a0002c0002t0001g0163a0002c0002t0001g0193others(2): Show | 5 | HG01123.hp1 HG02015.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(38): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094508 | ||||||
chrX:20094509 | T | C | 1 | a0008c0006t0001g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+22241A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094509 | ||||||
chrX:20094509 | TATATATG others(53): Show |
T | 23 | a0002c0002t0001g0145a0002c0002t0001g0155a0002c0002t0001g0170others(20): Show | 23 | HG00733.hp1 HG01081.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(64): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094509 | ||||||
chrX:20094510 | A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG02165.hp1 HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.130+22240T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | ||||||
chrX:20094510 | ATATATG | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0032others(8): Show | 11 | HG01099.hp1 HG01346.hp1 NA18971.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | ||||||
chrX:20094510 | ATATATGT others(25): Show |
A | 2 | a0002c0002t0010g0209a0010c0015t0008g0165 | 2 | NA19030.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.130+22208_130+2223 others(36): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | ||||||
chrX:20094511 | T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0119 | 2 | NA18966.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.130+22239A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094511 | ||||||
chrX:20094511 | TATATGTA others(51): Show |
T | 2 | a0002c0002t0001g0184a0002c0002t0001g0188 | 2 | HG01361.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.130+22181_130+2223 others(62): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094511 | ||||||
chrX:20094512 | A | ATG | 4 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0116others(1): Show | 4 | HG01981.hp2 HG02074.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22237_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | ||||||
chrX:20094512 | A | ATGTATAT others(19): Show |
1 | a0001c0013t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130+22237_130+2223 others(30): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | ||||||
chrX:20094512 | A | G | 10 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0050others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+22238T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | ||||||
chrX:20094512 | ATATG | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0037others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | ||||||
chrX:20094513 | T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG01255.hp1 HG02698.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+22237A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094513 | ||||||
chrX:20094513 | TATGTATA others(49): Show |
T | 3 | a0002c0002t0001g0176a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.130+22181_130+2223 others(60): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094513 | ||||||
chrX:20094514 | A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0027others(26): Show | 29 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.130+22236T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094514 | ||||||
chrX:20094514 | ATG | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0050others(8): Show | 11 | HG00609.hp1 HG01517.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094514 | ||||||
chrX:20094515 | T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0068others(1): Show | 4 | HG02135.hp1 NA18962.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22235A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094515 | ||||||
chrX:20094516 | G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0027others(34): Show | 37 | HG00642.hp1 HG00673.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.130+22234C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | ||||||
chrX:20094516 | GTA | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0115 | 2 | NA18957.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.130+22232_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | ||||||
chrX:20094516 | GTATA | G | 3 | a0001c0001t0001g0114a0002c0002t0001g0203a0005c0010t0001g0107 | 3 | HG03486.hp1 NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.130+22230_130+2223 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | ||||||
chrX:20094517 | T | C | 8 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0138others(5): Show | 8 | HG01070.hp2 HG02615.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+22233A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094517 | ||||||
chrX:20094518 | A | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0023others(7): Show | 10 | HG00738.hp1 HG01981.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+22232T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094518 | ||||||
chrX:20094518 | ATATATAT others(17): Show |
A | 3 | a0002c0002t0001g0194a0002c0002t0001g0196a0002c0002t0001g0197 | 3 | HG01243.hp1 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.130+22208_130+2223 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094518 | ||||||
chrX:20094519 | T | C | 2 | a0002c0002t0001g0136a0002c0002t0001g0141 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+22231A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094519 | ||||||
chrX:20094520 | A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0032others(11): Show | 14 | HG01099.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+22230T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094520 | ||||||
chrX:20094522 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130+22228T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094522 | ||||||
chrX:20094524 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130+22226T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094524 | ||||||
chrX:20094528 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.130+22222T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094528 | ||||||
chrX:20094530 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+22208_130+2221 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094530 | ||||||
chrX:20094532 | A | ATATATG | 1 | a0008c0006t0001g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+22217_130+2221 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094532 | ||||||
chrX:20094535 | TATATATG others(27): Show |
T | 3 | a0002c0002t0001g0144a0002c0002t0001g0148a0002c0002t0001g0149 | 3 | HG02257.hp2 HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.130+22181_130+2221 others(38): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094535 | ||||||
chrX:20094536 | ATATATG | A | 1 | a0001c0001t0001g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.130+22208_130+2221 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094536 | ||||||
chrX:20094538 | A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0082a0001c0001t0001g0102others(1): Show | 4 | HG02083.hp1 HG02293.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22212T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094538 | ||||||
chrX:20094540 | A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0005g0070others(1): Show | 4 | HG01123.hp2 HG01934.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22210T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | ||||||
chrX:20094540 | ATG | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0100others(1): Show | 4 | HG02135.hp1 NA18940.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2220 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | ||||||
chrX:20094540 | ATGTATAT others(30): Show |
A | 1 | a0002c0002t0001g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.130+22173_130+2220 others(41): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | ||||||
chrX:20094541 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130+22209A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094541 | ||||||
chrX:20094542 | G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0058others(12): Show | 15 | HG01346.hp2 HG01433.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+22208C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | ||||||
chrX:20094542 | G | GTA | 2 | a0001c0001t0001g0086a0001c0001t0005g0070 | 2 | HG01123.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.130+22206_130+2220 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | ||||||
chrX:20094542 | G | GTATATA | 1 | a0001c0001t0001g0059 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+22202_130+2220 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | ||||||
chrX:20094542 | G | GTATATAT others(1): Show |
1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.130+22200_130+2220 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | ||||||
chrX:20094542 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130+22207_130+2220 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | ||||||
chrX:20094544 | A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0032others(15): Show | 18 | HG01070.hp2 HG01981.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+22206T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094544 | ||||||
chrX:20094545 | T | TATAC | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130+22204_130+2220 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094545 | ||||||
chrX:20094546 | A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0046others(4): Show | 7 | HG01346.hp2 HG01433.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+22204T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094546 | ||||||
chrX:20094548 | A | G | 1 | a0001c0013t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130+22202T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094548 | ||||||
chrX:20094552 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.130+22197_130+2219 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | ||||||
chrX:20094552 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.130+22197_130+2219 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | ||||||
chrX:20094552 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+22197_130+2219 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | ||||||
chrX:20094555 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130+22181_130+2219 others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094555 | ||||||
chrX:20094557 | T | C | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+22193A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094557 | ||||||
chrX:20094559 | TATATATA others(3): Show |
T | 4 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0032others(1): Show | 4 | NA18971.hp1 NA18984.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22181_130+2219 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094559 | ||||||
chrX:20094561 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+22189A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094561 | ||||||
chrX:20094561 | TATATATA others(1): Show |
T | 5 | a0001c0001t0001g0034a0002c0002t0001g0136a0002c0002t0001g0199others(2): Show | 5 | HG02451.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094561 | ||||||
chrX:20094563 | TATATAC | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0074others(18): Show | 21 | HG01070.hp2 HG02145.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094563 | ||||||
chrX:20094565 | T | TATATAC | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.130+22184_130+2218 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094565 | ||||||
chrX:20094565 | TATAC | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(33): Show | 36 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094565 | ||||||
chrX:20094567 | TAC | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0024others(15): Show | 18 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094567 | ||||||
chrX:20094569 | C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 77 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.130+22181G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094569 | ||||||
chrX:20094577 | T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0064 | 2 | HG02132.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.130+22173A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094577 | ||||||
chrX:20094592 | A | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG01981.hp1 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22158T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094592 | ||||||
chrX:20095034 | C | T | 37 | a0001c0001t0001g0018a0002c0002t0001g0125a0002c0002t0001g0127others(34): Show | 37 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.130+21716G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095034 | ||||||
chrX:20095071 | TA | T | 2 | a0002c0002t0002g0139a0002c0003t0001g0017 | 2 | HG01070.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.130+21678delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095071 | ||||||
chrX:20095111 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+21639A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095111 | ||||||
chrX:20095124 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.130+21626T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095124 | ||||||
chrX:20095134 | C | T | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+21616G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095134 | ||||||
chrX:20095156 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130+21594A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095156 | ||||||
chrX:20095210 | T | TTTTG | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.130+21536_130+2153 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095210 | ||||||
chrX:20095210 | TTTTGTTT others(1): Show |
T | 2 | a0001c0001t0001g0085a0002c0002t0001g0205 | 2 | HG01074.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130+21532_130+2153 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095210 | ||||||
chrX:20095886 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.130+20864G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095886 | ||||||
chrX:20095972 | C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0087 | 3 | HG00673.hp1 NA18990.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.130+20778G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095972 | ||||||
chrX:20096006 | C | T | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+20744G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096006 | ||||||
chrX:20096013 | C | T | 69 | a0002c0002t0001g0125a0002c0002t0001g0127a0002c0002t0001g0133others(66): Show | 69 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.130+20737G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096013 | ||||||
chrX:20096081 | C | CA | 30 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(27): Show | 30 | HG01123.hp2 HG01255.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+20668dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | ||||||
chrX:20096081 | C | CAA | 3 | a0002c0002t0001g0205a0002c0003t0001g0014a0009c0009t0001g0020 | 3 | HG01891.hp1 HG02886.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.130+20667_130+2066 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | ||||||
chrX:20096081 | C | CAAA | 1 | a0002c0005t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130+20666_130+2066 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | ||||||
chrX:20096081 | CA | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0084others(3): Show | 6 | HG01069.hp1 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+20668delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | ||||||
chrX:20096118 | AAAAAG | A | 1 | a0002c0002t0001g0158 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.130+20627_130+2063 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096118 | ||||||
chrX:20096259 | C | CT | 2 | a0002c0005t0001g0121a0009c0009t0001g0020 | 2 | HG01256.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.130+20490dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096259 | ||||||
chrX:20096259 | CT | C | 6 | a0001c0001t0001g0071a0002c0002t0001g0140a0002c0002t0001g0158others(3): Show | 6 | HG01167.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+20490delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096259 | ||||||
chrX:20096397 | T | C | 5 | a0002c0002t0001g0176a0002c0002t0001g0205a0002c0005t0001g0121others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+20353A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096397 | ||||||
chrX:20096429 | C | CA | 7 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0072others(4): Show | 7 | HG01361.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+20320dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | ||||||
chrX:20096429 | CA | C | 40 | a0001c0001t0001g0085a0001c0001t0001g0098a0002c0002t0001g0125others(37): Show | 40 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.130+20320delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | ||||||
chrX:20096429 | CAA | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0176a0002c0002t0001g0205others(4): Show | 7 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+20319_130+2032 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | ||||||
chrX:20098036 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+18714T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098036 | ||||||
chrX:20098097 | G | A | 34 | a0002c0002t0001g0127a0002c0002t0001g0142a0002c0002t0001g0144others(31): Show | 34 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.130+18653C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098097 | ||||||
chrX:20098379 | CAGTT | C | 1 | a0001c0001t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.130+18367_130+1837 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098379 | ||||||
chrX:20098395 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.130+18355T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098395 | ||||||
chrX:20098446 | T | G | 3 | a0002c0002t0001g0125a0002c0002t0001g0145a0002c0002t0001g0170 | 3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.130+18304A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098446 | ||||||
chrX:20098506 | C | G | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+18244G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098506 | ||||||
chrX:20098557 | T | TG | 16 | a0001c0001t0001g0092a0001c0001t0001g0112a0002c0002t0001g0132others(13): Show | 16 | HG01070.hp2 HG01261.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+18192dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098557 | ||||||
chrX:20098557 | T | TGG | 1 | a0002c0002t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.130+18191_130+1819 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098557 | ||||||
chrX:20098560 | G | T | 2 | a0002c0002t0001g0125a0002c0002t0001g0170 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.130+18190C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098560 | ||||||
chrX:20098569 | C | CG | 2 | a0001c0001t0001g0024a0009c0009t0001g0020 | 2 | NA18953.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.130+18180dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098569 | ||||||
chrX:20098900 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.130+17850G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098900 | ||||||
chrX:20098948 | A | G | 1 | a0002c0003t0007g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+17802T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098948 | ||||||
chrX:20099225 | G | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0141a0002c0002t0001g0199others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+17525C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099225 | ||||||
chrX:20099235 | A | ACT | 2 | a0002c0002t0001g0185a0002c0002t0002g0186 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.130+17513_130+1751 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | ||||||
chrX:20099235 | ACT | A | 19 | a0001c0001t0001g0087a0002c0002t0001g0144a0002c0002t0001g0148others(16): Show | 19 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.130+17513_130+1751 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | ||||||
chrX:20099235 | ACTCT | A | 37 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0023others(34): Show | 37 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.130+17511_130+1751 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | ||||||
chrX:20099235 | ACTCTCT | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 142 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.130+17509_130+1751 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | ||||||
chrX:20099235 | ACTCTCTC others(1): Show |
A | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0141others(5): Show | 8 | HG01081.hp2 HG02300.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+17507_130+1751 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | ||||||
chrX:20099781 | C | A | 1 | a0011c0012t0001g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.130+16969G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099781 | ||||||
chrX:20100067 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+16683G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100067 | ||||||
chrX:20100394 | C | T | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+16356G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100394 | ||||||
chrX:20100683 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.130+16067G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100683 | ||||||
chrX:20100768 | T | G | 1 | a0005c0010t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+15982A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100768 | ||||||
chrX:20100793 | A | G | 18 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+15957T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100793 | ||||||
chrX:20100847 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130+15903G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100847 | ||||||
chrX:20101021 | C | CA | 10 | a0002c0002t0001g0134a0002c0002t0001g0151a0002c0002t0001g0166others(7): Show | 10 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+15728dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101021 | ||||||
chrX:20101021 | C | CAAA | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+15726_130+1572 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101021 | ||||||
chrX:20101021 | CA | C | 1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.130+15728delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101021 | ||||||
chrX:20101033 | A | C | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+15717T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101033 | ||||||
chrX:20101291 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.130+15459C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101291 | ||||||
chrX:20101816 | T | C | 8 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(5): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+14934A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101816 | ||||||
chrX:20102369 | C | T | 12 | a0002c0002t0001g0176a0002c0002t0001g0177a0002c0002t0001g0178others(9): Show | 12 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+14381G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102369 | ||||||
chrX:20102411 | T | G | 26 | a0001c0001t0001g0018a0002c0002t0001g0127a0002c0002t0001g0142others(23): Show | 26 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.130+14339A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102411 | ||||||
chrX:20102447 | T | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0013t0001g0190 | 3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.130+14303A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102447 | ||||||
chrX:20102821 | T | C | 98 | a0001c0001t0001g0018a0002c0002t0001g0001a0002c0002t0001g0125others(95): Show | 99 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.130+13929A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102821 | ||||||
chrX:20102935 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.130+13815A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102935 | ||||||
chrX:20103051 | C | T | 91 | a0001c0001t0001g0018a0002c0002t0001g0001a0002c0002t0001g0125others(88): Show | 92 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.130+13699G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103051 | ||||||
chrX:20103122 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.130+13628A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103122 | ||||||
chrX:20103290 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.130+13460G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103290 | ||||||
chrX:20103343 | G | C | 1 | a0002c0002t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+13407C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103343 | ||||||
chrX:20103408 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+13342G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103408 | ||||||
chrX:20103498 | T | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0141 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+13252A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103498 | ||||||
chrX:20103524 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+13226A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103524 | ||||||
chrX:20103623 | G | T | 83 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(80): Show | 84 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+13127C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103623 | ||||||
chrX:20103701 | C | T | 87 | a0002c0002t0001g0001a0002c0002t0001g0125a0002c0002t0001g0126others(84): Show | 88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.130+13049G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103701 | ||||||
chrX:20103914 | C | G | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+12836G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103914 | ||||||
chrX:20104013 | A | G | 2 | a0002c0005t0001g0122a0002c0005t0001g0123 | 2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.130+12737T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104013 | ||||||
chrX:20104332 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+12418C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104332 | ||||||
chrX:20104336 | T | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG01934.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+12414A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104336 | ||||||
chrX:20104445 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.130+12305G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104445 | ||||||
chrX:20104568 | TG | T | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+12181delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104568 | ||||||
chrX:20104752 | GGAAAGCT others(6): Show |
G | 1 | a0001c0001t0001g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.130+11985_130+1199 others(17): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104752 | ||||||
chrX:20104792 | C | T | 50 | a0001c0001t0001g0018a0002c0002t0001g0127a0002c0002t0001g0133others(47): Show | 50 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.130+11958G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104792 | ||||||
chrX:20105342 | A | C | 5 | a0002c0004t0001g0172a0002c0004t0001g0173a0002c0004t0001g0174others(2): Show | 5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11408T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20105342 | ||||||
chrX:20105421 | A | G | 1 | a0002c0002t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+11329T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20105421 | ||||||
chrX:20106366 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+10384C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106366 | ||||||
chrX:20106494 | T | C | 1 | a0002c0002t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+10256A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106494 | ||||||
chrX:20106859 | T | C | 1 | a0002c0002t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+9891A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106859 | ||||||
chrX:20106988 | GA | G | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.130+9761delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106988 | ||||||
chrX:20106990 | A | G | 1 | a0002c0002t0001g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+9760T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106990 | ||||||
chrX:20107076 | A | G | 1 | a0002c0002t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+9674T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107076 | ||||||
chrX:20107086 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.130+9664C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107086 | ||||||
chrX:20107495 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130+9255C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107495 | ||||||
chrX:20107573 | G | GC | 18 | a0001c0001t0001g0086a0001c0001t0001g0111a0002c0002t0001g0001others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+9176dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107573 | ||||||
chrX:20107617 | AT | A | 1 | a0002c0002t0001g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130+9132delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107617 | ||||||
chrX:20107772 | TA | T | 1 | a0002c0002t0001g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.130+8977delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107772 | ||||||
chrX:20107866 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+8884G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107866 | ||||||
chrX:20108032 | G | A | 5 | a0002c0002t0001g0205a0002c0005t0001g0121a0002c0005t0001g0122others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+8718C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108032 | ||||||
chrX:20108086 | G | GT | 1 | a0009c0009t0001g0020 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130+8663dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108086 | ||||||
chrX:20108239 | ATT | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 209 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(206): Show |
intron_variant | MODIFIER | c.130+8509_130+8510d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108239 | ||||||
chrX:20108720 | C | CA | 13 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0105others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+8029dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108720 | ||||||
chrX:20108720 | CA | C | 1 | a0002c0002t0001g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.130+8029delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108720 | ||||||
chrX:20108834 | GT | G | 5 | a0002c0002t0001g0205a0002c0005t0001g0121a0002c0005t0001g0122others(2): Show | 5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+7915delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108834 | ||||||
chrX:20108868 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+7882C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108868 | ||||||
chrX:20109169 | A | G | 13 | a0002c0002t0001g0001a0002c0002t0001g0126a0002c0002t0001g0128others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+7581T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109169 | ||||||
chrX:20109229 | T | G | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7521A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109229 | ||||||
chrX:20109248 | A | G | 91 | a0001c0001t0001g0018a0002c0002t0001g0001a0002c0002t0001g0125others(88): Show | 92 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.130+7502T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109248 | ||||||
chrX:20109357 | TA | T | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.130+7392delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109357 | ||||||
chrX:20109420 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130+7330A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109420 | ||||||
chrX:20109480 | A | ACT | 7 | a0002c0002t0001g0125a0002c0002t0001g0133a0002c0002t0001g0134others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+7268_130+7269d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109480 | ||||||
chrX:20109519 | C | CA | 10 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG00733.hp2 HG02027.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+7230dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | ||||||
chrX:20109519 | C | CAA | 1 | a0007c0007t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+7229_130+7230d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | ||||||
chrX:20109519 | CA | C | 46 | a0001c0001t0001g0105a0001c0001t0004g0016a0002c0002t0001g0001others(43): Show | 47 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.130+7230delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | ||||||
chrX:20109519 | CAA | C | 35 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0136others(32): Show | 35 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.130+7229_130+7230d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | ||||||
chrX:20109519 | CAAA | C | 4 | a0002c0002t0001g0144a0002c0002t0001g0148a0002c0002t0001g0149others(1): Show | 4 | HG02257.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7228_130+7230d others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | ||||||
chrX:20109634 | CT | C | 1 | a0004c0011t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+7115delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109634 | ||||||
chrX:20109811 | G | A | 3 | a0002c0003t0003g0094a0002c0003t0003g0095a0002c0003t0003g0096 | 3 | HG02015.hp1 HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.130+6939C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109811 | ||||||
chrX:20109989 | T | C | 1 | a0002c0002t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+6761A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109989 | ||||||
chrX:20110027 | C | T | 4 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0192others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6723G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110027 | ||||||
chrX:20110092 | C | CT | 4 | a0001c0001t0001g0012a0002c0002t0001g0144a0002c0002t0001g0145others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6657dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110092 | ||||||
chrX:20110092 | CT | C | 2 | a0002c0002t0002g0191a0002c0005t0001g0121 | 2 | HG01256.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.130+6657delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110092 | ||||||
chrX:20110605 | G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02027.hp1 NA18945.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6145C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110605 | ||||||
chrX:20110662 | C | CA | 13 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(10): Show | 13 | HG02109.hp1 HG02135.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+6087dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110662 | ||||||
chrX:20110662 | CA | C | 4 | a0001c0001t0001g0012a0002c0002t0001g0126a0002c0002t0001g0143others(1): Show | 4 | HG02630.hp1 HG03579.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6087delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110662 | ||||||
chrX:20110662 | CAA | C | 3 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02630.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.130+6086_130+6087d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110662 | ||||||
chrX:20110780 | T | C | 1 | a0002c0002t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.130+5970A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110780 | ||||||
chrX:20111127 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+5623G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111127 | ||||||
chrX:20111265 | A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | NA18979.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.130+5485T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111265 | ||||||
chrX:20111371 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.130+5379G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111371 | ||||||
chrX:20111426 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130+5324C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111426 | ||||||
chrX:20111517 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.130+5233G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111517 | ||||||
chrX:20111582 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+5168A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111582 | ||||||
chrX:20111629 | G | A | 1 | a0003c0016t0009g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+5121C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111629 | ||||||
chrX:20111645 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.130+5105C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111645 | ||||||
chrX:20112008 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.130+4742C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112008 | ||||||
chrX:20112009 | CG | C | 1 | a0002c0002t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.130+4740delC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112009 | ||||||
chrX:20112118 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.130+4632C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112118 | ||||||
chrX:20112327 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+4423G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112327 | ||||||
chrX:20113039 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.130+3711G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113039 | ||||||
chrX:20113244 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.130+3506T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113244 | ||||||
chrX:20113487 | G | A | 5 | a0002c0002t0001g0194a0002c0002t0001g0195a0002c0002t0001g0196others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+3263C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113487 | ||||||
chrX:20113579 | G | A | 4 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(1): Show | 4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3171C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113579 | ||||||
chrX:20113661 | C | CT | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+3088dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113661 | ||||||
chrX:20113929 | T | C | 1 | a0002c0004t0001g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130+2821A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113929 | ||||||
chrX:20113983 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.130+2767A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113983 | ||||||
chrX:20114223 | G | C | 1 | a0002c0002t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+2527C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114223 | ||||||
chrX:20114454 | GCAGATTG others(36): Show |
G | 1 | a0002c0002t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+2253_130+2295d others(45): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114454 | ||||||
chrX:20114459 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.130+2291A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114459 | ||||||
chrX:20114685 | C | T | 10 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(7): Show | 10 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+2065G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114685 | ||||||
chrX:20114756 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.130+1994A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114756 | ||||||
chrX:20114824 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+1926C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114824 | ||||||
chrX:20114985 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.130+1765C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114985 | ||||||
chrX:20115194 | T | TC | 1 | a0002c0003t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130+1555dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115194 | ||||||
chrX:20115239 | T | TA | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01496.hp2 HG02109.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+1510dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115239 | ||||||
chrX:20115239 | TA | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0005a0002c0002t0001g0001others(8): Show | 12 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+1510delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115239 | ||||||
chrX:20115253 | A | C | 1 | a0002c0002t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+1497T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115253 | ||||||
chrX:20115258 | AC | A | 2 | a0002c0002t0001g0205a0002c0005t0001g0121 | 2 | HG01256.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130+1491delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115258 | ||||||
chrX:20115259 | C | A | 3 | a0001c0001t0001g0118a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.130+1491G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115259 | ||||||
chrX:20115622 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.130+1128A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115622 | ||||||
chrX:20115666 | C | A | 3 | a0002c0002t0001g0205a0002c0005t0001g0122a0002c0005t0001g0123 | 3 | HG01496.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130+1084G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115666 | ||||||
chrX:20116221 | G | A | 1 | a0002c0004t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.130+529C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116221 | ||||||
chrX:20116546 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.130+204T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116546 | ||||||
chrX:20116595 | T | TC | 1 | a0002c0002t0010g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+154dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116595 | ||||||
chrX:20116694 | G | GC | 1 | a0001c0001t0001g0119 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.130+55dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116694 | ||||||
chrX:20116695 | C | T | 1 | a0002c0002t0002g0124 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.130+55G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116695 | ||||||
chrX:20116701 | C | A | 1 | a0002c0002t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130+49G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116701 |