geneid | 55344 |
---|---|
ensemblid | ENSG00000182378.15 |
hgncid | 23148 |
symbol | PLCXD1 |
name | phosphatidylinositol specific phospholipase C X domain containing 1 |
refseq_nuc | NM_018390.4 |
refseq_prot | NP_060860.1 |
ensembl_nuc | ENST00000381657.8 |
ensembl_prot | ENSP00000371073.2 |
mane_status | MANE Select |
chr | chrX |
start | 281381 |
end | 303356 |
strand | + |
ver | v1.2 |
region | chrX:281381-303356 |
region5000 | chrX:276381-308356 |
regionname0 | PLCXD1_chrX_281381_303356 |
regionname5000 | PLCXD1_chrX_276381_308356 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001 | 1/1 | 323 | 162 | 32 | 31 | 82 | 5 | 10 | 65 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002 | 0/0 | 323 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0003 | 0/0 | 323 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0004 | 0/0 | 202 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0005 | 0/0 | 202 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0006 | 0/0 | 61 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0007 | 0/0 | 214 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0008 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0009 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0010 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0011 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 972 | 90 | 14 | 9 | 58 | 4 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0002 | 1/1 | 972 | 33 | 1 | 12 | 13 | 0 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0003 | 0/0 | 972 | 31 | 16 | 9 | 5 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0004 | 0/0 | 972 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0005 | 0/0 | 972 | 2 | 1 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0006 | 0/0 | 972 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0007 | 0/0 | 972 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0008 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0009 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0010 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0011 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0012 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0013 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0014 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0015 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0016 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0017 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0018 | 0/0 | 971 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0019 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
c0020 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4349 | 13 | 0 | 5 | 6 | 2 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0002 | 0/0 | 4337 | 12 | 0 | 3 | 7 | 0 | 2 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0003 | 0/0 | 4349 | 6 | 0 | 0 | 6 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0004 | 0/0 | 4337 | 5 | 0 | 1 | 4 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0005 | 0/0 | 4349 | 5 | 0 | 0 | 5 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0006 | 0/0 | 4331 | 4 | 4 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0007 | 0/0 | 4335 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0008 | 0/0 | 4337 | 4 | 0 | 4 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0009 | 0/0 | 4349 | 3 | 0 | 2 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0010 | 0/0 | 4337 | 3 | 0 | 1 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0011 | 0/0 | 4340 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0012 | 0/0 | 4327 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0013 | 0/0 | 4346 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0014 | 0/0 | 4349 | 2 | 0 | 0 | 0 | 1 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0015 | 0/0 | 4340 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0016 | 0/0 | 4344 | 2 | 0 | 1 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0017 | 0/0 | 4331 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0018 | 0/0 | 4305 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0019 | 0/0 | 4335 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0020 | 0/0 | 4338 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0021 | 0/0 | 4338 | 2 | 0 | 0 | 1 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0022 | 0/0 | 4336 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0023 | 0/0 | 4334 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0024 | 0/0 | 4334 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0025 | 0/0 | 4334 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0026 | 0/0 | 4337 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0027 | 0/0 | 4329 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0028 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0029 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0030 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0031 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0032 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0033 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0034 | 0/0 | 4340 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0035 | 0/0 | 4337 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0036 | 0/0 | 4337 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0037 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0038 | 0/0 | 4334 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0039 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0040 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0041 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0042 | 0/0 | 4333 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0043 | 0/0 | 4344 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0044 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0045 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0046 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0047 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0048 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0049 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0050 | 0/0 | 4339 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0051 | 0/0 | 4333 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0052 | 0/0 | 4333 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0053 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0054 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0055 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0056 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0057 | 0/0 | 4352 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0058 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0059 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0060 | 0/0 | 4336 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0061 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0062 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0063 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0064 | 0/1 | 4349 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0065 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0066 | 0/0 | 4351 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0067 | 0/0 | 4351 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0068 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0069 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0070 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0071 | 0/0 | 4332 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0072 | 0/0 | 4348 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0073 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0074 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0075 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0076 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0077 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0078 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0079 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0080 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0081 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0082 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0083 | 0/0 | 4333 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0084 | 0/0 | 4344 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0085 | 0/0 | 4434 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0086 | 0/0 | 4332 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0087 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0088 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0089 | 0/0 | 4343 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0090 | 0/0 | 4343 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0091 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0092 | 0/0 | 4339 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0093 | 0/0 | 4339 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0094 | 0/0 | 4336 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0095 | 0/0 | 4334 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0096 | 1/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0097 | 0/0 | 4337 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0098 | 0/0 | 4337 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0099 | 0/0 | 4338 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0100 | 0/0 | 4337 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0101 | 0/0 | 4334 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0102 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0103 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0104 | 0/0 | 4333 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0105 | 0/0 | 4351 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0106 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0107 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0108 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0109 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0110 | 0/0 | 4338 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0111 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0112 | 0/0 | 4348 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0113 | 0/0 | 4339 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
t0114 | 0/0 | 4343 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018 | 0/0 | 971 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001 | 0/0 | 972 | 90 | 14 | 9 | 58 | 4 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002 | 1/1 | 972 | 33 | 1 | 12 | 13 | 0 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003 | 0/0 | 972 | 31 | 16 | 9 | 5 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0004 | 0/0 | 972 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0006 | 0/0 | 972 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0009 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0010 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0014 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002c0005 | 0/0 | 972 | 2 | 1 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002c0019 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0003c0007 | 0/0 | 972 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0004c0017 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0005c0015 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0006c0020 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0007c0012 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0008c0011 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0009c0013 | 0/0 | 972 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0010c0008 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0011c0016 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018t0101 | 0/0 | 5304 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0001 | 0/0 | 5320 | 10 | 0 | 3 | 5 | 2 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0002 | 0/0 | 5308 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0003 | 0/0 | 5320 | 5 | 0 | 0 | 5 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0004 | 0/0 | 5308 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0005 | 0/0 | 5320 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0007 | 0/0 | 5306 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0009 | 0/0 | 5320 | 3 | 0 | 2 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0010 | 0/0 | 5308 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0011 | 0/0 | 5311 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0012 | 0/0 | 5298 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0013 | 0/0 | 5317 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0014 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0015 | 0/0 | 5311 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0016 | 0/0 | 5315 | 2 | 0 | 1 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0017 | 0/0 | 5302 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0018 | 0/0 | 5276 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0024 | 0/0 | 5305 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0025 | 0/0 | 5305 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0026 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0027 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0028 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0029 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0030 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0031 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0032 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0033 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0034 | 0/0 | 5311 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0037 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0041 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0043 | 0/0 | 5315 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0045 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0048 | 0/0 | 5301 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0050 | 0/0 | 5310 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0052 | 0/0 | 5304 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0057 | 0/0 | 5323 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0059 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0061 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0066 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0067 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0068 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0069 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0070 | 0/0 | 5312 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0071 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0072 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0073 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0074 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0078 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0079 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0080 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0083 | 0/0 | 5304 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0084 | 0/0 | 5315 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0085 | 0/0 | 5405 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0086 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0087 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0092 | 0/0 | 5310 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0095 | 0/0 | 5305 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0099 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0103 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0111 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0113 | 0/0 | 5310 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0001t0114 | 0/0 | 5314 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0001 | 0/0 | 5320 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0002 | 0/0 | 5308 | 5 | 0 | 1 | 2 | 0 | 2 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0004 | 0/0 | 5308 | 3 | 0 | 1 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0008 | 0/0 | 5308 | 4 | 0 | 4 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0010 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0019 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0038 | 0/0 | 5305 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0039 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0046 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0047 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0049 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0064 | 0/1 | 5320 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0076 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0090 | 0/0 | 5314 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0091 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0093 | 0/0 | 5310 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0094 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0096 | 1/0 | 5318 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0097 | 0/0 | 5308 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0098 | 0/0 | 5308 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0100 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0105 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0002t0110 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0002 | 0/0 | 5308 | 5 | 0 | 2 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0006 | 0/0 | 5302 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0014 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0020 | 0/0 | 5309 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0023 | 0/0 | 5305 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0035 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0036 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0044 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0051 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0053 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0054 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0055 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0056 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0058 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0060 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0063 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0065 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0081 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0082 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0088 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0089 | 0/0 | 5314 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0104 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0003t0107 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0004t0007 | 0/0 | 5306 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0004t0112 | 0/0 | 5319 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0006t0003 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0006t0075 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0009t0102 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0010t0042 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0001c0014t0062 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002c0005t0022 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002c0005t0106 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0002c0019t0022 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0003c0007t0019 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0003c0007t0021 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0004c0017t0040 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0005c0015t0109 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0006c0020t0001 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0007c0012t0005 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0008c0011t0108 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0009c0013t0021 | 0/0 | 5309 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0010c0008t0077 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
a0011c0016t0006 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | copy fasta | chrX | 276381 | 308356 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018t0101g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0014g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0016g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0017g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0024g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0025g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0026g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0027g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0028g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0029g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0030g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0031g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0032g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0033g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0034g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0037g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0041g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0043g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0045g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0048g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0050g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0052g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0057g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0059g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0061g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0066g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0067g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0068g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0069g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0070g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0071g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0072g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0073g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0074g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0078g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0079g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0080g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0083g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0084g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0085g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0086g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0087g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0092g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0095g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0099g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0103g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0111g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0113g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0114g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0010g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0019g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0038g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0039g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0046g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0047g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0049g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0064g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0076g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0090g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0091g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0093g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0094g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0096g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0097g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0098g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0100g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0105g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0110g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0014g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0020g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0020g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0023g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0035g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0036g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0044g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0051g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0053g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0054g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0055g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0056g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0058g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0060g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0063g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0065g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0081g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0082g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0088g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0089g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0104g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0107g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0112g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0006t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0006t0075g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0009t0102g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0010t0042g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0014t0062g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0005t0022g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0005t0106g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0019t0022g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0003c0007t0019g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0003c0007t0021g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0004c0017t0040g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0005c0015t0109g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0006c0020t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0007c0012t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0008c0011t0108g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0009c0013t0021g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0010c0008t0077g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0011c0016t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00099 | hp2 | a0001 | c0003 | t0014 | g0048 | EUR | GBR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00280 | hp1 | a0001 | c0001 | t0095 | g0097 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00323 | hp2 | a0001 | c0001 | t0072 | g0001 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00408 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00408 | hp2 | a0001 | c0001 | t0066 | g0161 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00423 | hp1 | a0001 | c0001 | t0067 | g0039 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00423 | hp2 | a0001 | c0001 | t0010 | g0087 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00438 | hp1 | a0001 | c0001 | t0061 | g0033 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00438 | hp2 | a0001 | c0001 | t0041 | g0164 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00544 | hp1 | a0003 | c0007 | t0021 | g0009 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00544 | hp2 | a0001 | c0001 | t0083 | g0085 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00558 | hp1 | a0003 | c0007 | t0019 | g0009 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00609 | hp1 | a0001 | c0001 | t0048 | g0030 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00639 | hp1 | a0002 | c0019 | t0022 | g0138 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00639 | hp2 | a0001 | c0002 | t0008 | g0157 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00735 | hp1 | a0002 | c0005 | t0022 | g0035 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00735 | hp2 | a0001 | c0001 | t0026 | g0064 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00738 | hp1 | a0001 | c0002 | t0093 | g0137 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01070 | hp2 | a0001 | c0003 | t0020 | g0056 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01109 | hp1 | a0001 | c0003 | t0020 | g0036 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0044 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01168 | hp2 | a0001 | c0003 | t0060 | g0051 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0018 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01175 | hp2 | a0001 | c0003 | t0063 | g0049 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01261 | hp1 | a0001 | c0002 | t0100 | g0008 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01346 | hp1 | a0001 | c0014 | t0062 | g0095 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01346 | hp2 | a0001 | c0001 | t0016 | g0098 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01361 | hp1 | a0001 | c0002 | t0008 | g0116 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01361 | hp2 | a0001 | c0001 | t0071 | g0052 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0067 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01496 | hp2 | a0001 | c0003 | t0036 | g0006 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01891 | hp1 | a0001 | c0003 | t0006 | g0114 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01891 | hp2 | a0001 | c0001 | t0086 | g0061 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01943 | hp2 | a0001 | c0002 | t0010 | g0008 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01975 | hp1 | a0001 | c0002 | t0110 | g0129 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01975 | hp2 | a0001 | c0002 | t0004 | g0133 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01993 | hp1 | a0000 | c0018 | t0101 | g0132 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02056 | hp1 | a0001 | c0001 | t0029 | g0019 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02080 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02148 | hp1 | a0001 | c0002 | t0008 | g0131 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0065 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02155 | hp1 | a0001 | c0006 | t0003 | g0118 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02155 | hp2 | a0001 | c0001 | t0045 | g0031 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02165 | hp1 | a0007 | c0012 | t0005 | g0001 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02257 | hp1 | a0002 | c0005 | t0106 | g0077 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02257 | hp2 | a0001 | c0003 | t0055 | g0010 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02280 | hp1 | a0001 | c0003 | t0056 | g0092 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0074 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02293 | hp1 | a0001 | c0002 | t0008 | g0117 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02293 | hp2 | a0001 | c0003 | t0035 | g0006 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02615 | hp1 | a0001 | c0003 | t0053 | g0162 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02615 | hp2 | a0001 | c0003 | t0051 | g0071 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02622 | hp1 | a0001 | c0003 | t0058 | g0103 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0100 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02630 | hp1 | a0011 | c0016 | t0006 | g0076 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02630 | hp2 | a0008 | c0011 | t0108 | g0022 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0126 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02683 | hp1 | a0001 | c0002 | t0097 | g0141 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02683 | hp2 | a0001 | c0002 | t0098 | g0136 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02723 | hp1 | a0010 | c0008 | t0077 | g0072 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02723 | hp2 | a0001 | c0003 | t0023 | g0020 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0007 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02886 | hp2 | a0001 | c0003 | t0023 | g0021 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02896 | hp1 | a0001 | c0001 | t0114 | g0013 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02896 | hp2 | a0001 | c0003 | t0088 | g0152 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02922 | hp1 | a0001 | c0002 | t0090 | g0151 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02922 | hp2 | a0001 | c0003 | t0006 | g0042 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0125 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03017 | hp1 | a0001 | c0001 | t0085 | g0090 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0007 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03130 | hp1 | a0001 | c0003 | t0107 | g0104 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03139 | hp1 | a0001 | c0003 | t0044 | g0115 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03195 | hp1 | a0001 | c0001 | t0018 | g0099 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03195 | hp2 | a0001 | c0003 | t0006 | g0041 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03486 | hp1 | a0001 | c0001 | t0034 | g0069 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03486 | hp2 | a0001 | c0003 | t0104 | g0093 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03516 | hp1 | a0001 | c0001 | t0087 | g0060 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0134 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03669 | hp2 | a0009 | c0013 | t0021 | g0150 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03927 | hp1 | a0001 | c0002 | t0094 | g0140 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03927 | hp2 | a0001 | c0001 | t0084 | g0091 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04184 | hp1 | a0001 | c0001 | t0014 | g0083 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04184 | hp2 | a0001 | c0001 | t0092 | g0089 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04199 | hp1 | a0001 | c0001 | t0016 | g0082 | SAS | STU | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | STU | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | CHB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18906 | hp1 | a0001 | c0003 | t0054 | g0094 | AFR | YRI | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18906 | hp2 | a0001 | c0010 | t0042 | g0163 | AFR | YRI | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18941 | hp1 | a0001 | c0001 | t0025 | g0079 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18941 | hp2 | a0001 | c0002 | t0038 | g0153 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18942 | hp2 | a0001 | c0004 | t0112 | g0105 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18944 | hp1 | a0001 | c0002 | t0047 | g0144 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18947 | hp1 | a0001 | c0004 | t0007 | g0106 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18947 | hp2 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18948 | hp1 | a0001 | c0001 | t0030 | g0062 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18950 | hp1 | a0001 | c0001 | t0078 | g0080 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18950 | hp2 | a0001 | c0001 | t0079 | g0001 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18951 | hp1 | a0001 | c0004 | t0007 | g0110 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18954 | hp2 | a0001 | c0009 | t0102 | g0032 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0146 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18956 | hp2 | a0001 | c0001 | t0111 | g0014 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18961 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18964 | hp2 | a0001 | c0001 | t0052 | g0068 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18969 | hp1 | a0001 | c0001 | t0032 | g0058 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18969 | hp2 | a0006 | c0020 | t0001 | g0111 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18972 | hp2 | a0001 | c0002 | t0039 | g0127 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18980 | hp1 | a0001 | c0001 | t0037 | g0063 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18980 | hp2 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18985 | hp1 | a0001 | c0002 | t0004 | g0109 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18986 | hp1 | a0001 | c0003 | t0081 | g0057 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18988 | hp1 | a0001 | c0002 | t0019 | g0130 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18991 | hp1 | a0001 | c0001 | t0113 | g0166 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18991 | hp2 | a0001 | c0001 | t0068 | g0034 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18992 | hp1 | a0001 | c0001 | t0057 | g0055 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18993 | hp1 | a0001 | c0001 | t0024 | g0101 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18993 | hp2 | a0001 | c0006 | t0075 | g0112 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18998 | hp1 | a0001 | c0001 | t0099 | g0120 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18999 | hp1 | a0001 | c0001 | t0103 | g0037 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19003 | hp1 | a0001 | c0003 | t0082 | g0160 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19003 | hp2 | a0001 | c0002 | t0091 | g0155 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19006 | hp1 | a0004 | c0017 | t0040 | g0165 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19009 | hp1 | a0001 | c0001 | t0027 | g0059 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19011 | hp1 | a0001 | c0001 | t0050 | g0043 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19011 | hp2 | a0001 | c0001 | t0028 | g0070 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19055 | hp1 | a0001 | c0002 | t0076 | g0107 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19056 | hp1 | a0001 | c0001 | t0069 | g0148 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19057 | hp1 | a0001 | c0001 | t0070 | g0004 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19057 | hp2 | a0001 | c0001 | t0033 | g0078 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19060 | hp1 | a0001 | c0001 | t0074 | g0143 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19062 | hp1 | a0005 | c0015 | t0109 | g0113 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19063 | hp1 | a0001 | c0001 | t0031 | g0066 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19074 | hp1 | a0001 | c0001 | t0080 | g0088 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19074 | hp2 | a0001 | c0001 | t0073 | g0102 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19080 | hp1 | a0001 | c0002 | t0046 | g0145 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19081 | hp2 | a0001 | c0002 | t0049 | g0023 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19086 | hp1 | a0001 | c0002 | t0105 | g0128 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19090 | hp1 | a0001 | c0001 | t0059 | g0123 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01123 | hp1 | a0001 | c0001 | t0043 | g0017 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01123 | hp2 | a0001 | c0003 | t0065 | g0012 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02559 | hp1 | a0001 | c0003 | t0089 | g0011 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02559 | hp2 | a0001 | c0001 | t0015 | g0073 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0064 | g0156 | REF | REF | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0096 | g0119 | REF | REF | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
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:284212
|
A | G | 1 | a0003 | 2 | HG00544.hp1 HG00558.hp1 |
missense_variant | MODERATE | c.25A>G | p.Asn9Asp | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 350/5318 | 25/972 | 9/323 | chrX | 284212 | ||
chrX:284271
|
T | TC | 1 | a0004 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.88dupC | p.Arg30fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 414/5318 | 89/972 | 30/323 | INFO_REALIGN_3_PRIME | chrX | 284271 | |
chrX:284275
|
C | T | 1 | a0011 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.88C>T | p.Arg30Trp | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 413/5318 | 88/972 | 30/323 | chrX | 284275 | ||
chrX:288771
|
T | TC | 1 | a0005 | 1 | NA19062.hp1 | frameshift_variant | HIGH | c.171dupC | p.Ile58fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/7 | 497/5318 | 172/972 | 58/323 | INFO_REALIGN_3_PRIME | chrX | 288771 | |
chrX:288788
|
G | GT | 1 | a0006 | 1 | NA18969.hp2 | frameshift_variant&stop_gained | HIGH | c.183_184insT | p.Glu62fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/7 | 509/5318 | 184/972 | 62/323 | chrX | 288788 | ||
chrX:288799
|
T | TG | 1 | a0006 | 1 | NA18969.hp2 | frameshift_variant | HIGH | c.195dupG | p.Leu66fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/7 | 521/5318 | 196/972 | 66/323 | INFO_REALIGN_3_PRIME | chrX | 288799 | |
chrX:288824
|
GC | G | 1 | a0006 | 1 | NA18969.hp2 | frameshift_variant | HIGH | c.222delC | p.Cys75fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/7 | 547/5318 | 222/972 | 74/323 | INFO_REALIGN_3_PRIME | chrX | 288824 | |
chrX:290728
|
GA | G | 1 | a0006 | 1 | NA18969.hp2 | frameshift_variant | HIGH | c.347delA | p.Lys116fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/7 | 672/5318 | 347/972 | 116/323 | INFO_REALIGN_3_PRIME | chrX | 290728 | |
chrX:291610
|
G | A | 1 | a0010 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.505G>A | p.Ala169Thr | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/7 | 830/5318 | 505/972 | 169/323 | chrX | 291610 | ||
chrX:293130
|
G | A | 1 | a0007 | 1 | HG02165.hp1 | stop_gained | HIGH | c.645G>A | p.Trp215* | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/7 | 970/5318 | 645/972 | 215/323 | chrX | 293130 | ||
chrX:299156
|
C | T | 1 | a0009 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.793C>T | p.Pro265Ser | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1118/5318 | 793/972 | 265/323 | chrX | 299156 | ||
chrX:299198
|
C | G | 1 | a0008 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.835C>G | p.Arg279Gly | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1160/5318 | 835/972 | 279/323 | chrX | 299198 | ||
chrX:299277
|
G | T | 1 | a0002 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.914G>T | p.Gly305Val | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1239/5318 | 914/972 | 305/323 | chrX | 299277 | ||
chrX:299284
|
CG | C | 1 | a0000 | 1 | HG01993.hp1 | frameshift_variant | HIGH | c.923delG | p.Gly308fs | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1248/5318 | 923/972 | 308/323 | INFO_REALIGN_3_PRIME | chrX | 299284 |
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:284193
|
T | C | 12 | a0001c0001a0001c0003a0001c0009others(9): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
synonymous_variant | LOW | c.6T>C | p.Gly2Gly | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 331/5318 | 6/972 | 2/323 | chrX | 284193 | ||
chrX:290695
|
C | T | 6 | a0001c0001a0001c0006a0001c0014others(3): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
synonymous_variant | LOW | c.312C>T | p.Asp104Asp | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/7 | 637/5318 | 312/972 | 104/323 | chrX | 290695 | ||
chrX:291609
|
C | T | 3 | a0001c0004a0001c0014a0006c0020 | 5 | HG01346.hp1 NA18942.hp2 NA18947.hp1 others(2): Show |
synonymous_variant | LOW | c.504C>T | p.Val168Val | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/7 | 829/5318 | 504/972 | 168/323 | chrX | 291609 | ||
chrX:299293
|
C | T | 1 | a0001c0010 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.930C>T | p.Val310Val | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1255/5318 | 930/972 | 310/323 | chrX | 299293 | ||
chrX:299320
|
G | A | 1 | a0001c0009 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.957G>A | p.Lys319Lys | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1282/5318 | 957/972 | 319/323 | chrX | 299320 |
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:281393
|
AG | A | 1 | a0001c0001t0024 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-310delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2792 | INFO_REALIGN_3_PRIME | chrX | 281393 | ||||
chrX:281411
|
T | C | 14 | a0001c0001t0009a0001c0001t0025a0001c0001t0026others(11): Show | 16 | HG00735.hp2 HG01496.hp1 HG01496.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-295T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2777 | chrX | 281411 | |||||
chrX:281423
|
TG | T | 1 | a0001c0001t0025 | 1 | NA18941.hp1 | 5_prime_UTR_variant | MODIFIER | c.-281delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2763 | INFO_REALIGN_3_PRIME | chrX | 281423 | ||||
chrX:281446
|
CT | C | 1 | a0001c0002t0038 | 1 | NA18941.hp2 | 5_prime_UTR_variant | MODIFIER | c.-256delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2738 | INFO_REALIGN_3_PRIME | chrX | 281446 | ||||
chrX:281450
|
TG | T | 1 | a0001c0002t0039 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2735 | INFO_REALIGN_3_PRIME | chrX | 281450 | ||||
chrX:281507
|
T | TG | 1 | a0001c0001t0114 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2678 | INFO_REALIGN_3_PRIME | chrX | 281507 | ||||
chrX:281554
|
CG | C | 1 | a0004c0017t0040 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2631 | INFO_REALIGN_3_PRIME | chrX | 281554 | ||||
chrX:281629
|
C | CT | 1 | a0001c0001t0113 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2557 | INFO_REALIGN_3_PRIME | chrX | 281629 | ||||
chrX:281640
|
AC | A | 1 | a0001c0001t0041 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2546 | INFO_REALIGN_3_PRIME | chrX | 281640 | ||||
chrX:281662
|
TC | T | 1 | a0001c0004t0112 | 1 | NA18942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2521 | INFO_REALIGN_3_PRIME | chrX | 281662 | ||||
chrX:281674
|
T | TG | 1 | a0001c0001t0114 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/7 | 2510 | INFO_REALIGN_3_PRIME | chrX | 281674 | ||||
chrX:284167
|
G | GT | 1 | a0001c0001t0111 | 1 | NA18956.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 18 | INFO_REALIGN_3_PRIME | chrX | 284167 | ||||
chrX:284170
|
GC | G | 2 | a0001c0001t0114a0001c0002t0039 | 2 | HG02896.hp1 NA18972.hp2 |
5_prime_UTR_variant | MODIFIER | c.-15delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/7 | 15 | INFO_REALIGN_3_PRIME | chrX | 284170 | ||||
chrX:299379
|
C | G | 1 | a0001c0002t0110 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 44 | chrX | 299379 | |||||
chrX:299383
|
G | A | 1 | a0001c0010t0042 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 48 | chrX | 299383 | |||||
chrX:299412
|
G | A | 3 | a0001c0001t0011a0001c0001t0043a0001c0003t0044 | 4 | HG01123.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*77G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 77 | chrX | 299412 | |||||
chrX:299482
|
T | C | 1 | a0001c0001t0045 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 147 | chrX | 299482 | |||||
chrX:299487
|
G | A | 1 | a0001c0010t0042 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 152 | chrX | 299487 | |||||
chrX:299498
|
G | A | 12 | a0001c0001t0004a0001c0001t0026a0001c0001t0041others(9): Show | 15 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*163G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 163 | chrX | 299498 | |||||
chrX:299517
|
T | TGG | 1 | a0005c0015t0109 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184_*185dupGG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 186 | INFO_REALIGN_3_PRIME | chrX | 299517 | ||||
chrX:299587
|
A | G | 6 | a0001c0003t0023a0001c0003t0107a0002c0005t0022others(3): Show | 7 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*252A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 252 | chrX | 299587 | |||||
chrX:299614
|
TG | T | 1 | a0005c0015t0109 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 282 | INFO_REALIGN_3_PRIME | chrX | 299614 | ||||
chrX:299629
|
C | T | 1 | a0001c0002t0105 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 294 | chrX | 299629 | |||||
chrX:299630
|
G | A | 1 | a0001c0003t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 295 | chrX | 299630 | |||||
chrX:299687
|
A | G | 6 | a0001c0003t0023a0001c0003t0107a0002c0005t0022others(3): Show | 7 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*352A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 352 | chrX | 299687 | |||||
chrX:299691
|
A | T | 1 | a0001c0003t0104 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 356 | chrX | 299691 | |||||
chrX:299761
|
G | GA | 1 | a0001c0001t0057 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 436 | INFO_REALIGN_3_PRIME | chrX | 299761 | ||||
chrX:299771
|
C | A | 10 | a0001c0001t0027a0001c0001t0052a0001c0003t0006others(7): Show | 12 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*436C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 436 | chrX | 299771 | |||||
chrX:299781
|
T | C | 1 | a0001c0003t0058 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 446 | chrX | 299781 | |||||
chrX:299800
|
C | A | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(47): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*465C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 465 | chrX | 299800 | |||||
chrX:299826
|
C | T | 4 | a0001c0003t0023a0001c0003t0058a0001c0003t0107others(1): Show | 5 | HG02622.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 491 | chrX | 299826 | |||||
chrX:299871
|
T | C | 4 | a0001c0001t0083a0001c0001t0084a0001c0003t0081others(1): Show | 4 | HG00544.hp2 HG03927.hp2 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*536T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 536 | chrX | 299871 | |||||
chrX:299878
|
AC | A | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(65): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*547delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 547 | INFO_REALIGN_3_PRIME | chrX | 299878 | ||||
chrX:299881
|
C | T | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(65): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*546C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 546 | chrX | 299881 | |||||
chrX:299905
|
C | T | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(64): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 570 | chrX | 299905 | |||||
chrX:299935
|
G | C | 84 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(81): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*600G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 600 | chrX | 299935 | |||||
chrX:299956
|
G | A | 2 | a0001c0002t0046a0001c0002t0047 | 2 | NA18944.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*621G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 621 | chrX | 299956 | |||||
chrX:299978
|
G | A | 1 | a0001c0001t0028 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 643 | chrX | 299978 | |||||
chrX:300011
|
C | T | 2 | a0001c0003t0023a0008c0011t0108 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*676C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 676 | chrX | 300011 | |||||
chrX:300015
|
T | C | 3 | a0001c0001t0083a0001c0003t0081a0001c0003t0082 | 3 | HG00544.hp2 NA18986.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*680T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 680 | chrX | 300015 | |||||
chrX:300052
|
C | CA | 6 | a0001c0001t0029a0001c0001t0030a0001c0001t0059others(3): Show | 6 | HG02056.hp1 HG04184.hp2 NA18906.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*738dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 739 | INFO_REALIGN_3_PRIME | chrX | 300052 | ||||
chrX:300052
|
CA | C | 34 | a0000c0018t0101a0001c0001t0007a0001c0001t0011others(31): Show | 41 | HG00323.hp2 HG01123.hp1 HG01891.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*738delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 738 | INFO_REALIGN_3_PRIME | chrX | 300052 | ||||
chrX:300052
|
CAA | C | 5 | a0001c0003t0023a0001c0003t0107a0002c0005t0022others(2): Show | 6 | HG00639.hp1 HG00735.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*737_*738delAA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 737 | INFO_REALIGN_3_PRIME | chrX | 300052 | ||||
chrX:300052
|
CAAA | C | 2 | a0001c0003t0104a0002c0005t0106 | 2 | HG02257.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*736_*738delAAA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 736 | INFO_REALIGN_3_PRIME | chrX | 300052 | ||||
chrX:300073
|
AG | A | 1 | a0001c0003t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 739 | chrX | 300073 | |||||
chrX:300098
|
G | A | 1 | a0001c0003t0053 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*763G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 763 | chrX | 300098 | |||||
chrX:300178
|
A | G | 3 | a0001c0001t0014a0001c0001t0071a0001c0003t0014 | 3 | HG00099.hp2 HG01361.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*843A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 843 | chrX | 300178 | |||||
chrX:300232
|
G | A | 10 | a0001c0001t0011a0001c0001t0015a0001c0001t0017others(7): Show | 13 | HG01123.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*897G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 897 | chrX | 300232 | |||||
chrX:300239
|
T | A | 1 | a0001c0003t0054 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 904 | chrX | 300239 | |||||
chrX:300243
|
A | G | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(47): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 908 | chrX | 300243 | |||||
chrX:300320
|
CCT | C | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*986_*987delCT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 986 | chrX | 300320 | |||||
chrX:300396
|
GTGTC | G | 3 | a0001c0001t0015a0001c0001t0034a0001c0001t0114 | 4 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1065_*1068delCTGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1065 | INFO_REALIGN_3_PRIME | chrX | 300396 | ||||
chrX:300438
|
G | A | 7 | a0001c0003t0006a0001c0003t0053a0001c0003t0054others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1103G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1103 | chrX | 300438 | |||||
chrX:300440
|
A | G | 7 | a0001c0003t0006a0001c0003t0053a0001c0003t0054others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1105 | chrX | 300440 | |||||
chrX:300442
|
G | A | 7 | a0001c0003t0006a0001c0003t0053a0001c0003t0054others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1107G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1107 | chrX | 300442 | |||||
chrX:300442
|
G | GTA | 73 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(70): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1109_*1110dupAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1111 | INFO_REALIGN_3_PRIME | chrX | 300442 | ||||
chrX:300458
|
GTA | G | 3 | a0002c0005t0022a0002c0005t0106a0002c0019t0022 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1127_*1128delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1127 | INFO_REALIGN_3_PRIME | chrX | 300458 | ||||
chrX:300462
|
ATG | A | 12 | a0000c0018t0101a0001c0001t0048a0001c0001t0083others(9): Show | 12 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1143_*1144delGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1143 | INFO_REALIGN_3_PRIME | chrX | 300462 | ||||
chrX:300462
|
ATGTG | A | 1 | a0001c0001t0011 | 2 | HG02647.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1141_*1144delGTGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1141 | INFO_REALIGN_3_PRIME | chrX | 300462 | ||||
chrX:300468
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135_*1146delGTGT others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1135 | INFO_REALIGN_3_PRIME | chrX | 300468 | ||||
chrX:300470
|
G | A | 79 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(76): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1135 | chrX | 300470 | |||||
chrX:300474
|
GTGTGTAT others(1): Show |
G | 1 | a0001c0001t0070 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145_*1152delATAT others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1145 | INFO_REALIGN_3_PRIME | chrX | 300474 | ||||
chrX:300482
|
ATGTG | A | 4 | a0001c0001t0095a0002c0005t0022a0002c0005t0106others(1): Show | 4 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1151_*1154delGTGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1151 | INFO_REALIGN_3_PRIME | chrX | 300482 | ||||
chrX:300488
|
G | A | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1153 | chrX | 300488 | |||||
chrX:300490
|
ATG | A | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1161_*1162delGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1161 | INFO_REALIGN_3_PRIME | chrX | 300490 | ||||
chrX:300496
|
G | T | 1 | a0001c0001t0069 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1161 | chrX | 300496 | |||||
chrX:300496
|
GTATA | G | 1 | a0001c0001t0027 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165_*1168delATAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1165 | INFO_REALIGN_3_PRIME | chrX | 300496 | ||||
chrX:300504
|
GTA | G | 20 | a0001c0001t0011a0001c0001t0012a0001c0001t0015others(17): Show | 25 | HG00639.hp1 HG00735.hp1 HG01123.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1173_*1174delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1173 | INFO_REALIGN_3_PRIME | chrX | 300504 | ||||
chrX:300506
|
ATATG | A | 1 | a0001c0003t0058 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173_*1176delATGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1173 | INFO_REALIGN_3_PRIME | chrX | 300506 | ||||
chrX:300508
|
A | G | 2 | a0001c0001t0018a0001c0001t0052 | 3 | HG02622.hp2 HG03195.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1173A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1173 | chrX | 300508 | |||||
chrX:300527
|
C | T | 1 | a0001c0002t0100 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1192 | chrX | 300527 | |||||
chrX:300532
|
A | G | 5 | a0001c0001t0003a0001c0001t0067a0001c0001t0111others(2): Show | 9 | HG00423.hp1 HG02135.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1197 | chrX | 300532 | |||||
chrX:300534
|
G | A | 1 | a0001c0002t0093 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1199G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1199 | chrX | 300534 | |||||
chrX:300536
|
ATACATGT others(29): Show |
A | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1217_*1252delATGC others(32): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1217 | INFO_REALIGN_3_PRIME | chrX | 300536 | ||||
chrX:300542
|
GTA | G | 16 | a0001c0001t0011a0001c0001t0012a0001c0001t0015others(13): Show | 21 | HG01123.hp1 HG01346.hp2 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1211_*1212delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1211 | INFO_REALIGN_3_PRIME | chrX | 300542 | ||||
chrX:300544
|
A | ATGTGTAT others(81): Show |
1 | a0001c0001t0085 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insGTGT others(84): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1211 | INFO_REALIGN_3_PRIME | chrX | 300544 | ||||
chrX:300558
|
GTA | G | 3 | a0001c0001t0027a0001c0001t0052a0001c0001t0083 | 3 | HG00544.hp2 NA18964.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227_*1228delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1227 | INFO_REALIGN_3_PRIME | chrX | 300558 | ||||
chrX:300566
|
GTA | G | 7 | a0001c0003t0006a0001c0003t0053a0001c0003t0054others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1233_*1234delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1233 | INFO_REALIGN_3_PRIME | chrX | 300566 | ||||
chrX:300578
|
GTA | G | 4 | a0001c0001t0017a0001c0001t0071a0001c0001t0086others(1): Show | 5 | HG01361.hp2 HG01891.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1247_*1248delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1247 | INFO_REALIGN_3_PRIME | chrX | 300578 | ||||
chrX:300588
|
T | G | 63 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(60): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1253T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1253 | chrX | 300588 | |||||
chrX:300596
|
GTA | G | 3 | a0002c0005t0022a0002c0005t0106a0002c0019t0022 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1265_*1266delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1265 | INFO_REALIGN_3_PRIME | chrX | 300596 | ||||
chrX:300600
|
ATG | A | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1271_*1272delGT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1271 | INFO_REALIGN_3_PRIME | chrX | 300600 | ||||
chrX:300619
|
C | T | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1284C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1284 | chrX | 300619 | |||||
chrX:300643
|
T | C | 1 | a0001c0001t0033 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1308 | chrX | 300643 | |||||
chrX:300644
|
G | A | 1 | a0001c0003t0044 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1309 | chrX | 300644 | |||||
chrX:300649
|
C | T | 2 | a0001c0003t0023a0001c0003t0051 | 3 | HG02615.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1314C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1314 | chrX | 300649 | |||||
chrX:300650
|
G | A | 15 | a0001c0001t0011a0001c0001t0015a0001c0001t0016others(12): Show | 19 | HG01123.hp1 HG01346.hp2 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1315G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1315 | chrX | 300650 | |||||
chrX:300650
|
G | T | 3 | a0001c0001t0005a0001c0001t0078a0007c0012t0005 | 6 | HG02080.hp1 HG02165.hp1 HG02165.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1315G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1315 | chrX | 300650 | |||||
chrX:300692
|
GTA | G | 1 | a0001c0003t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369_*1370delAT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1369 | INFO_REALIGN_3_PRIME | chrX | 300692 | ||||
chrX:300795
|
C | T | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1460C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1460 | chrX | 300795 | |||||
chrX:300807
|
A | C | 1 | a0001c0003t0082 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1472 | chrX | 300807 | |||||
chrX:300879
|
A | T | 22 | a0001c0001t0007a0001c0001t0018a0001c0001t0024others(19): Show | 28 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1544A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1544 | chrX | 300879 | |||||
chrX:300904
|
C | T | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1569C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1569 | chrX | 300904 | |||||
chrX:300955
|
G | C | 2 | a0001c0001t0027a0001c0001t0052 | 2 | NA18964.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1620G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1620 | chrX | 300955 | |||||
chrX:300978
|
C | T | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1643C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1643 | chrX | 300978 | |||||
chrX:300995
|
G | A | 1 | a0001c0001t0017 | 2 | HG02886.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1660G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1660 | chrX | 300995 | |||||
chrX:301002
|
C | T | 1 | a0001c0010t0042 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1667C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1667 | chrX | 301002 | |||||
chrX:301069
|
G | C | 13 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(10): Show | 16 | HG02622.hp1 HG02630.hp2 HG02723.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1734G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1734 | chrX | 301069 | |||||
chrX:301147
|
G | A | 24 | a0001c0001t0007a0001c0001t0012a0001c0001t0017others(21): Show | 31 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1812G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1812 | chrX | 301147 | |||||
chrX:301191
|
G | C | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1856G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1856 | chrX | 301191 | |||||
chrX:301213
|
A | G | 3 | a0001c0001t0017a0001c0001t0086a0001c0001t0087 | 4 | HG01891.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1878A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1878 | chrX | 301213 | |||||
chrX:301215
|
G | T | 5 | a0001c0001t0012a0001c0001t0017a0001c0001t0086others(2): Show | 7 | HG01891.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1880G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1880 | chrX | 301215 | |||||
chrX:301244
|
C | G | 51 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(48): Show | 69 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1909C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1909 | chrX | 301244 | |||||
chrX:301353
|
A | C | 3 | a0001c0001t0017a0001c0001t0086a0001c0001t0087 | 4 | HG01891.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2018A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2018 | chrX | 301353 | |||||
chrX:301378
|
A | G | 3 | a0001c0001t0017a0001c0001t0086a0001c0001t0087 | 4 | HG01891.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2043A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2043 | chrX | 301378 | |||||
chrX:301389
|
C | G | 7 | a0001c0003t0006a0001c0003t0053a0001c0003t0054others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2054C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2054 | chrX | 301389 | |||||
chrX:301393
|
C | G | 1 | a0001c0003t0104 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2058 | chrX | 301393 | |||||
chrX:301393
|
C | T | 20 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(17): Show | 25 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2058C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2058 | chrX | 301393 | |||||
chrX:301447
|
A | ATTGT | 77 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(74): Show | 102 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2114_*2115insGTTT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2115 | INFO_REALIGN_3_PRIME | chrX | 301447 | ||||
chrX:301447
|
A | ATTGTT | 1 | a0001c0001t0099 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2114_*2115insGTTT others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2115 | INFO_REALIGN_3_PRIME | chrX | 301447 | ||||
chrX:301464
|
G | A | 11 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(8): Show | 14 | HG02630.hp2 HG02723.hp2 HG02886.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2129G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2129 | chrX | 301464 | |||||
chrX:301532
|
C | T | 10 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(7): Show | 12 | HG02630.hp2 HG02723.hp1 NA18941.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2197C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2197 | chrX | 301532 | |||||
chrX:301556
|
G | A | 1 | a0001c0003t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2221G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2221 | chrX | 301556 | |||||
chrX:301622
|
T | G | 1 | a0001c0003t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2287T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2287 | chrX | 301622 | |||||
chrX:301625
|
T | G | 13 | a0001c0001t0012a0001c0001t0017a0001c0001t0086others(10): Show | 17 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2290T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2290 | chrX | 301625 | |||||
chrX:301695
|
A | G | 2 | a0001c0001t0086a0001c0001t0087 | 2 | HG01891.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2360A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2360 | chrX | 301695 | |||||
chrX:301735
|
T | C | 1 | a0001c0003t0104 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2400 | chrX | 301735 | |||||
chrX:301751
|
G | C | 1 | a0001c0001t0030 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2416 | chrX | 301751 | |||||
chrX:301760
|
G | A | 2 | a0001c0003t0035a0001c0003t0036 | 2 | HG01496.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2425G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2425 | chrX | 301760 | |||||
chrX:301781
|
G | A | 3 | a0001c0001t0012a0001c0003t0058a0001c0003t0104 | 4 | HG02622.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2446G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2446 | chrX | 301781 | |||||
chrX:301908
|
G | A | 19 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(16): Show | 23 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2573G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2573 | chrX | 301908 | |||||
chrX:301993
|
C | A | 21 | a0000c0018t0101a0001c0001t0004a0001c0001t0010others(18): Show | 28 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2658C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2658 | chrX | 301993 | |||||
chrX:302004
|
G | C | 78 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(75): Show | 103 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2669G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2669 | chrX | 302004 | |||||
chrX:302007
|
A | G | 120 | a0000c0018t0101a0001c0001t0001a0001c0001t0002others(117): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2672A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2672 | chrX | 302007 | |||||
chrX:302061
|
G | GT | 1 | a0001c0001t0057 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2728dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2729 | INFO_REALIGN_3_PRIME | chrX | 302061 | ||||
chrX:302110
|
A | G | 21 | a0001c0001t0007a0001c0001t0017a0001c0001t0024others(18): Show | 27 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2775A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2775 | chrX | 302110 | |||||
chrX:302123
|
G | A | 1 | a0001c0002t0097 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2788G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2788 | chrX | 302123 | |||||
chrX:302168
|
G | C | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2833G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2833 | chrX | 302168 | |||||
chrX:302177
|
C | T | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2842C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2842 | chrX | 302177 | |||||
chrX:302247
|
AAAGTCCT others(8): Show |
A | 77 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(74): Show | 101 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2916_*2930delTCCT others(11): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2916 | INFO_REALIGN_3_PRIME | chrX | 302247 | ||||
chrX:302270
|
A | AC | 72 | a0000c0018t0101a0001c0001t0001a0001c0001t0002others(69): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2945dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2946 | INFO_REALIGN_3_PRIME | chrX | 302270 | ||||
chrX:302270
|
A | ACC | 13 | a0001c0001t0057a0001c0001t0092a0001c0001t0095others(10): Show | 14 | HG00280.hp1 HG00544.hp1 HG01070.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2944_*2945dupCC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2946 | INFO_REALIGN_3_PRIME | chrX | 302270 | ||||
chrX:302270
|
A | ACCC | 5 | a0001c0001t0050a0001c0001t0066a0001c0001t0067others(2): Show | 5 | HG00408.hp2 HG00423.hp1 NA18950.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2943_*2945dupCCC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2946 | INFO_REALIGN_3_PRIME | chrX | 302270 | ||||
chrX:302270
|
AC | A | 24 | a0001c0001t0007a0001c0001t0012a0001c0001t0024others(21): Show | 30 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2945delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2945 | INFO_REALIGN_3_PRIME | chrX | 302270 | ||||
chrX:302270
|
ACC | A | 2 | a0001c0001t0027a0001c0001t0052 | 2 | NA18964.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2944_*2945delCC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2944 | INFO_REALIGN_3_PRIME | chrX | 302270 | ||||
chrX:302314
|
G | A | 1 | a0001c0003t0089 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2979G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2979 | chrX | 302314 | |||||
chrX:302378
|
G | A | 2 | a0001c0003t0054a0001c0003t0056 | 2 | HG02280.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3043G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3043 | chrX | 302378 | |||||
chrX:302427
|
CTT | C | 5 | a0001c0001t0016a0001c0001t0084a0001c0001t0085others(2): Show | 6 | HG01346.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3093_*3094delTT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3093 | chrX | 302427 | |||||
chrX:302450
|
A | G | 56 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(53): Show | 75 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3115A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3115 | chrX | 302450 | |||||
chrX:302459
|
TCTCAG | T | 1 | a0001c0001t0048 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3129_*3133delGCTC others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3129 | INFO_REALIGN_3_PRIME | chrX | 302459 | ||||
chrX:302483
|
T | C | 5 | a0000c0018t0101a0001c0002t0008a0001c0002t0100others(2): Show | 8 | HG00639.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3148T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3148 | chrX | 302483 | |||||
chrX:302538
|
C | T | 1 | a0001c0002t0064 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3203C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3203 | chrX | 302538 | |||||
chrX:302590
|
G | C | 59 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(56): Show | 77 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3255G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3255 | chrX | 302590 | |||||
chrX:302594
|
C | T | 59 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(56): Show | 77 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3259C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3259 | chrX | 302594 | |||||
chrX:302601
|
T | A | 1 | a0001c0014t0062 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3266 | chrX | 302601 | |||||
chrX:302744
|
T | G | 1 | a0001c0003t0035 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3409T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3409 | chrX | 302744 | |||||
chrX:302762
|
C | T | 7 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(4): Show | 9 | NA18941.hp1 NA18947.hp1 NA18947.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3427C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3427 | chrX | 302762 | |||||
chrX:302833
|
C | T | 12 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(9): Show | 14 | HG02280.hp1 HG02630.hp2 HG02723.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3498C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3498 | chrX | 302833 | |||||
chrX:302834
|
A | G | 22 | a0001c0001t0007a0001c0001t0012a0001c0001t0018others(19): Show | 29 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3499A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3499 | chrX | 302834 | |||||
chrX:302837
|
G | C | 22 | a0001c0001t0007a0001c0001t0012a0001c0001t0018others(19): Show | 29 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3502G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3502 | chrX | 302837 | |||||
chrX:302876
|
T | G | 1 | a0001c0002t0098 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3541T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3541 | chrX | 302876 | |||||
chrX:302934
|
A | G | 2 | a0001c0001t0024a0001c0002t0076 | 2 | NA18993.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3599A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3599 | chrX | 302934 | |||||
chrX:302964
|
TCCC | T | 1 | a0001c0003t0107 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630_*3632delCCC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3630 | chrX | 302964 | |||||
chrX:302965
|
C | A | 19 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(16): Show | 24 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3630C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3630 | chrX | 302965 | |||||
chrX:302966
|
C | T | 2 | a0008c0011t0108a0010c0008t0077 | 2 | HG02630.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3631C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3631 | chrX | 302966 | |||||
chrX:302991
|
A | G | 1 | a0001c0003t0107 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3656A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3656 | chrX | 302991 | |||||
chrX:303093
|
G | A | 5 | a0001c0003t0006a0001c0003t0053a0001c0003t0055others(2): Show | 7 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3758G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3758 | chrX | 303093 | |||||
chrX:303108
|
A | AC | 5 | a0001c0001t0031a0001c0001t0059a0001c0001t0079others(2): Show | 5 | HG01175.hp2 HG01891.hp2 NA18950.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3776dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3777 | INFO_REALIGN_3_PRIME | chrX | 303108 | ||||
chrX:303214
|
G | A | 1 | a0001c0003t0053 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3879G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3879 | chrX | 303214 | |||||
chrX:303214
|
G | C | 1 | a0001c0003t0020 | 2 | HG01070.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3879G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3879 | chrX | 303214 | |||||
chrX:303264
|
G | A | 7 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(4): Show | 9 | NA18941.hp1 NA18947.hp1 NA18947.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3929G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3929 | chrX | 303264 | |||||
chrX:303311
|
G | A | 61 | a0000c0018t0101a0001c0001t0002a0001c0001t0004others(58): Show | 80 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*3976G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 3976 | chrX | 303311 |
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:281722
|
T | TTC | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+41_-22+42dupTC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281722 | |||||
chrX:281733
|
G | GGC | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+49_-22+50insGC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281733 | ||||||
chrX:281735
|
C | CG | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-22+55dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281735 | |||||
chrX:281735
|
C | G | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+51C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281735 | ||||||
chrX:281740
|
C | CT | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+58dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281740 | |||||
chrX:281748
|
CT | C | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-22+66delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281748 | |||||
chrX:281767
|
C | G | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22+83C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281767 | ||||||
chrX:281781
|
CAG | C | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-22+100_-22+101del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281781 | |||||
chrX:281791
|
C | T | 3 | a0001c0001t0066g0161a0001c0003t0002g0159a0001c0003t0082g0160 | 3 | HG00408.hp2 NA18992.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-22+107C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281791 | ||||||
chrX:281804
|
G | A | 3 | a0001c0003t0055g0010a0001c0003t0065g0012a0001c0003t0089g0011 | 3 | HG01123.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-22+120G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281804 | ||||||
chrX:281824
|
T | TC | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+140_-22+141ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281824 | ||||||
chrX:281825
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-22+141T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281825 | ||||||
chrX:281825
|
T | G | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+141T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281825 | ||||||
chrX:281860
|
G | GC | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+178dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281860 | |||||
chrX:281904
|
C | CG | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+222dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281904 | |||||
chrX:281932
|
G | GA | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+251dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281932 | |||||
chrX:281946
|
C | CA | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+262_-22+263ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281946 | ||||||
chrX:281952
|
TG | T | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+270delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 281952 | |||||
chrX:282015
|
TG | T | 2 | a0001c0001t0113g0166a0001c0003t0002g0159 | 2 | NA18991.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-22+334delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282015 | |||||
chrX:282042
|
C | T | 5 | a0001c0001t0017g0007a0001c0003t0055g0010a0001c0003t0065g0012others(2): Show | 6 | HG01123.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+358C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282042 | ||||||
chrX:282043
|
C | CCG | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+359_-22+360ins others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282043 | ||||||
chrX:282045
|
G | T | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+361G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282045 | ||||||
chrX:282103
|
G | GC | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+419_-22+420ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282103 | ||||||
chrX:282131
|
TG | T | 1 | a0001c0004t0112g0105 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-22+450delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282131 | |||||
chrX:282229
|
A | C | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+545A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282229 | ||||||
chrX:282253
|
A | AC | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+570dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282253 | |||||
chrX:282280
|
G | T | 2 | a0001c0003t0053g0162a0001c0003t0058g0103 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-22+596G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282280 | ||||||
chrX:282314
|
G | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22+630G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282314 | ||||||
chrX:282314
|
G | GGA | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+632_-22+633dup others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282314 | |||||
chrX:282356
|
T | TG | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+675dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282356 | |||||
chrX:282380
|
CT | C | 1 | a0001c0001t0111g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-22+699delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282380 | |||||
chrX:282383
|
T | TA | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+707dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282383 | |||||
chrX:282383
|
TA | T | 2 | a0001c0001t0041g0164a0001c0001t0113g0166 | 2 | HG00438.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-22+707delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282383 | |||||
chrX:282389
|
AAAC | A | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-22+708_-22+710del others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282389 | |||||
chrX:282392
|
C | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22+708C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282392 | ||||||
chrX:282397
|
C | A | 2 | a0001c0001t0012g0015a0001c0003t0058g0103 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+713C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282397 | ||||||
chrX:282402
|
C | A | 2 | a0001c0001t0012g0015a0001c0003t0053g0162 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+718C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282402 | ||||||
chrX:282402
|
C | CA | 1 | a0001c0004t0007g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-22+728dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282402 | |||||
chrX:282402
|
CA | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-22+728delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282402 | |||||
chrX:282402
|
CAAA | C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22+726_-22+728del others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282402 | |||||
chrX:282405
|
A | C | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-22+721A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282405 | ||||||
chrX:282407
|
A | C | 23 | a0001c0001t0001g0086a0001c0001t0001g0158a0001c0001t0005g0084others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22+723A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282407 | ||||||
chrX:282408
|
A | C | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-22+724A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282408 | ||||||
chrX:282419
|
A | C | 2 | a0001c0001t0005g0081a0001c0001t0078g0080 | 2 | NA18950.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-22+735A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282419 | ||||||
chrX:282466
|
AG | A | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+784delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282466 | |||||
chrX:282510
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-22+826G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282510 | ||||||
chrX:282533
|
C | CG | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+850dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282533 | |||||
chrX:282536
|
C | CCTT | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+852_-22+853ins others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282536 | ||||||
chrX:282537
|
T | C | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+853T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282537 | ||||||
chrX:282540
|
AC | A | 1 | a0001c0003t0002g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-22+858delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282540 | |||||
chrX:282542
|
CA | C | 2 | a0001c0001t0024g0101a0001c0003t0081g0057 | 2 | NA18986.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-22+863delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282542 | |||||
chrX:282573
|
C | CG | 2 | a0001c0001t0025g0079a0004c0017t0040g0165 | 2 | NA18941.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-22+892dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282573 | |||||
chrX:282586
|
TC | T | 1 | a0001c0001t0032g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-22+905delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282586 | |||||
chrX:282631
|
G | C | 1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-22+947G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282631 | ||||||
chrX:282658
|
T | TC | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+975dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282658 | |||||
chrX:282703
|
C | CA | 37 | a0001c0001t0001g0086a0001c0001t0003g0024a0001c0001t0003g0025others(34): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.-22+1035dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282703 | |||||
chrX:282703
|
C | CAA | 3 | a0001c0001t0024g0101a0001c0001t0111g0014a0001c0003t0058g0103 | 3 | HG02622.hp1 NA18956.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-22+1034_-22+1035d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282703 | |||||
chrX:282703
|
CA | C | 6 | a0001c0001t0033g0078a0001c0002t0001g0154a0001c0002t0038g0153others(3): Show | 6 | HG00733.hp2 HG01070.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+1035delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282703 | |||||
chrX:282727
|
C | CA | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-22+1049dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282727 | |||||
chrX:282727
|
CA | C | 1 | a0001c0001t0111g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-22+1049delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282727 | |||||
chrX:282741
|
A | T | 2 | a0002c0005t0106g0077a0011c0016t0006g0076 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-22+1057A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282741 | ||||||
chrX:282744
|
C | T | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22+1060C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282744 | ||||||
chrX:282752
|
G | A | 1 | a0001c0009t0102g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-22+1068G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282752 | ||||||
chrX:282784
|
T | TC | 1 | a0001c0004t0112g0105 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-22+1102dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282784 | |||||
chrX:282795
|
A | AG | 1 | a0001c0001t0111g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-22+1114dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282795 | |||||
chrX:282805
|
C | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-22+1121C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282805 | ||||||
chrX:282815
|
C | CA | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+1133dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282815 | |||||
chrX:282836
|
T | C | 5 | a0001c0004t0007g0106a0001c0004t0007g0110a0001c0004t0112g0105others(2): Show | 5 | NA18942.hp2 NA18947.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+1152T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282836 | ||||||
chrX:282858
|
G | T | 22 | a0001c0001t0001g0086a0001c0001t0005g0084a0001c0001t0005g0096others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22+1174G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282858 | ||||||
chrX:282884
|
ATG | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0086a0001c0001t0005g0084others(19): Show | 23 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22+1204_-22+1205d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282884 | |||||
chrX:282888
|
GT | G | 1 | a0001c0004t0112g0105 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-22+1206delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282888 | |||||
chrX:282892
|
T | C | 3 | a0001c0001t0012g0015a0002c0005t0106g0077a0011c0016t0006g0076 | 3 | HG02257.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+1208T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282892 | ||||||
chrX:282933
|
GTTATATA others(4): Show |
G | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-21-1214_-21-1204d others(13): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282933 | |||||
chrX:282934
|
TTA | T | 2 | a0001c0003t0058g0103a0001c0009t0102g0032 | 2 | HG02622.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-21-1223_-21-1222d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282934 | |||||
chrX:282943
|
TATTA | T | 4 | a0001c0001t0012g0015a0001c0003t0053g0162a0002c0005t0106g0077others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-1223_-21-1220d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282943 | ||||||
chrX:282943
|
TATTATA | T | 20 | a0001c0001t0001g0086a0001c0001t0005g0084a0001c0001t0005g0096others(17): Show | 20 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21-1223_-21-1218d others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282943 | ||||||
chrX:282945
|
TTA | T | 31 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0009g0075others(28): Show | 32 | HG00735.hp2 HG01123.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-21-1212_-21-1211d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282945 | |||||
chrX:282951
|
A | G | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-1216A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282951 | ||||||
chrX:282957
|
T | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-1210T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282957 | ||||||
chrX:282958
|
A | T | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-1209A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282958 | ||||||
chrX:282964
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21-1185_-21-1168d others(20): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 282964 | |||||
chrX:283013
|
AT | A | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21-1153delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283013 | ||||||
chrX:283048
|
T | C | 2 | a0001c0001t0061g0033a0001c0001t0068g0034 | 2 | HG00438.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-21-1119T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283048 | ||||||
chrX:283067
|
A | ATG | 3 | a0001c0001t0012g0149a0001c0001t0113g0166a0009c0013t0021g0150 | 3 | HG03516.hp2 HG03669.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-21-1078_-21-1077d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283067 | |||||
chrX:283067
|
ATGTG | A | 3 | a0001c0001t0009g0075a0001c0003t0006g0114a0001c0003t0044g0115 | 3 | HG01891.hp1 HG03139.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-21-1080_-21-1077d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283067 | |||||
chrX:283067
|
ATGTGTG | A | 22 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0015g0073others(19): Show | 22 | HG00735.hp2 HG01496.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-21-1082_-21-1077d others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283067 | |||||
chrX:283067
|
ATGTGTGT others(1): Show |
A | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.-21-1084_-21-1077d others(10): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283067 | |||||
chrX:283067
|
ATGTGTGT others(5): Show |
A | 9 | a0001c0001t0012g0015a0001c0001t0017g0007a0001c0001t0086g0061others(6): Show | 10 | HG01123.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-1088_-21-1077d others(14): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283067 | |||||
chrX:283080
|
TGTGTG | T | 1 | a0001c0001t0024g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-21-1086_-21-1082d others(7): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283080 | ||||||
chrX:283114
|
T | TGGTTTTA others(2): Show |
1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21-1051_-21-1043d others(11): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283114 | |||||
chrX:283129
|
G | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-1038G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283129 | ||||||
chrX:283244
|
G | C | 1 | a0001c0001t0016g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-21-923G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283244 | ||||||
chrX:283260
|
C | CA | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-21-894dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283260 | |||||
chrX:283260
|
C | CAA | 22 | a0001c0001t0001g0086a0001c0001t0005g0084a0001c0001t0005g0096others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-21-895_-21-894dup others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283260 | |||||
chrX:283260
|
C | CAAA | 1 | a0001c0001t0016g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-21-896_-21-894dup others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283260 | |||||
chrX:283260
|
C | CAAAA | 1 | a0001c0001t0014g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-21-897_-21-894dup others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283260 | |||||
chrX:283274
|
C | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 57 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-21-893C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283274 | ||||||
chrX:283338
|
C | T | 2 | a0002c0005t0106g0077a0011c0016t0006g0076 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-21-829C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283338 | ||||||
chrX:283380
|
A | AG | 1 | a0001c0001t0111g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-21-785dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283380 | |||||
chrX:283425
|
GC | G | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-21-740delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283425 | |||||
chrX:283500
|
T | G | 2 | a0002c0005t0106g0077a0011c0016t0006g0076 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-21-667T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283500 | ||||||
chrX:283518
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-21-649A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283518 | ||||||
chrX:283523
|
A | AGTGGGGG others(77): Show |
1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-21-632_-21-631ins others(84): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283523 | |||||
chrX:283523
|
A | AGTGGGGG others(21): Show |
2 | a0001c0003t0006g0114a0001c0003t0044g0115 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-21-631_-21-604dup others(28): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283523 | |||||
chrX:283523
|
A | AGTGGGGG others(77): Show |
1 | a0001c0001t0034g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21-604_-21-603ins others(84): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283523 | |||||
chrX:283523
|
A | AGTGGGGG others(161): Show |
2 | a0001c0001t0086g0061a0001c0001t0087g0060 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-21-632_-21-631ins others(168): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283523 | |||||
chrX:283525
|
T | TG | 1 | a0005c0015t0109g0113 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-21-637dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283525 | |||||
chrX:283536
|
G | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-21-631G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283536 | ||||||
chrX:283536
|
G | GTGGTGTC others(217): Show |
1 | a0001c0001t0017g0007 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-21-604_-21-603ins others(224): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283536 | |||||
chrX:283536
|
G | T | 1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-21-631G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283536 | ||||||
chrX:283542
|
TCAGGCCC others(49): Show |
T | 1 | a0001c0003t0081g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-21-603_-21-548del others(56): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283542 | |||||
chrX:283564
|
T | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-21-603T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283564 | ||||||
chrX:283570
|
TCAGGCCC others(21): Show |
T | 2 | a0002c0005t0106g0077a0011c0016t0006g0076 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-21-572_-21-545del others(28): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283570 | |||||
chrX:283576
|
C | A | 1 | a0001c0001t0017g0007 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-21-591C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283576 | ||||||
chrX:283581
|
T | TGGGGGCG others(218): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-21-576_-21-575ins others(225): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283581 | |||||
chrX:283585
|
GGC | G | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-580_-21-579del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283585 | |||||
chrX:283591
|
C | G | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-576C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283591 | ||||||
chrX:283592
|
G | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-21-575G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283592 | ||||||
chrX:283595
|
GTGCCAGG others(2): Show |
G | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-571_-21-563del others(9): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283595 | ||||||
chrX:283598
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-21-569C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283598 | ||||||
chrX:283598
|
CCAGGCCC others(49): Show |
C | 1 | a0008c0011t0108g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-21-547_-21-492del others(56): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283598 | |||||
chrX:283604
|
C | CCGGGTGG others(161): Show |
5 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0114g0013others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-467_-21-466ins others(168): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283604 | |||||
chrX:283606
|
G | C | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-561G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283606 | ||||||
chrX:283610
|
GGGGGCGG others(4): Show |
G | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-555_-21-545del others(11): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283610 | |||||
chrX:283615
|
C | A | 2 | a0001c0004t0007g0106a0001c0004t0007g0110 | 2 | NA18947.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-21-552C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283615 | ||||||
chrX:283620
|
G | T | 1 | a0001c0002t0004g0146 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-21-547G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283620 | ||||||
chrX:283623
|
T | G | 6 | a0001c0001t0086g0061a0001c0001t0087g0060a0001c0002t0004g0146others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-544T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283623 | ||||||
chrX:283626
|
C | T | 2 | a0001c0002t0004g0146a0001c0003t0081g0057 | 2 | NA18956.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-21-541C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283626 | ||||||
chrX:283626
|
CCAGGCCC others(21): Show |
C | 6 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0003t0053g0162others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-507_-21-480del others(28): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283626 | |||||
chrX:283632
|
C | CCGGGTGG others(49): Show |
1 | a0001c0001t0005g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-21-522_-21-467dup others(56): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283632 | |||||
chrX:283637
|
TG | T | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-525delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283637 | |||||
chrX:283654
|
T | TCAGGCAC others(273): Show |
1 | a0001c0002t0004g0146 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-21-508_-21-507ins others(280): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283654 | |||||
chrX:283654
|
T | TCAGGCCC others(49): Show |
19 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-21-467_-21-466ins others(56): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283654 | |||||
chrX:283654
|
T | TCAGGCCC others(301): Show |
3 | a0001c0002t0004g0109a0001c0002t0046g0145a0001c0002t0047g0144 | 3 | NA18944.hp1 NA18985.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-21-467_-21-466ins others(308): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283654 | |||||
chrX:283660
|
CCGGGTGG others(21): Show |
C | 1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21-494_-21-467del others(28): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283660 | |||||
chrX:283661
|
C | T | 1 | a0001c0003t0081g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-21-506C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283661 | ||||||
chrX:283663
|
G | GA | 1 | a0001c0001t0111g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-21-504_-21-503ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283663 | ||||||
chrX:283688
|
A | ACGGGTGG others(301): Show |
1 | a0001c0001t0028g0070 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-21-467_-21-466ins others(308): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283688 | |||||
chrX:283688
|
A | C | 16 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0009g0075others(13): Show | 16 | HG00735.hp2 HG01496.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-479A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283688 | ||||||
chrX:283693
|
T | TG | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-469dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283693 | |||||
chrX:283715
|
A | G | 2 | a0001c0001t0086g0061a0001c0001t0087g0060 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-21-452A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283715 | ||||||
chrX:283757
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 58 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-21-410C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283757 | ||||||
chrX:283783
|
C | T | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-384C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283783 | ||||||
chrX:283858
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-21-309C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283858 | ||||||
chrX:283863
|
CCTCT | C | 1 | a0001c0002t0008g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-21-291_-21-288del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283863 | |||||
chrX:283871
|
T | TC | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-295dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283871 | |||||
chrX:283876
|
CTCT | C | 2 | a0001c0001t0045g0031a0001c0001t0048g0030 | 2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-21-289_-21-287del others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283876 | |||||
chrX:283878
|
CT | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-21-277delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 283878 | |||||
chrX:283880
|
T | C | 20 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(17): Show | 20 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21-287T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283880 | ||||||
chrX:284020
|
G | C | 3 | a0001c0001t0005g0081a0001c0001t0005g0084a0001c0001t0078g0080 | 3 | NA18612.hp1 NA18950.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-21-147G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 284020 | ||||||
chrX:284368
|
T | TG | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+58dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284368 | |||||
chrX:284470
|
CACAT | C | 2 | a0001c0003t0020g0036a0001c0003t0020g0056 | 2 | HG01070.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127+160_127+163del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284470 | |||||
chrX:284490
|
G | A | 1 | a0001c0006t0003g0118 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.127+176G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 284490 | ||||||
chrX:284503
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.127+189C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 284503 | ||||||
chrX:284583
|
TGCACACA others(1): Show |
T | 75 | a0000c0018t0101g0132a0001c0001t0007g0121a0001c0001t0007g0124others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.127+293_127+300del others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284583 | |||||
chrX:284583
|
TGCACACA others(9): Show |
T | 15 | a0001c0001t0012g0015a0001c0001t0015g0073a0001c0001t0015g0074others(12): Show | 16 | HG01891.hp1 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.127+285_127+300del others(16): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284583 | |||||
chrX:284592
|
GCACACAC others(3): Show |
G | 2 | a0001c0001t0074g0143a0001c0001t0113g0166 | 2 | NA18991.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.127+284_127+293del others(10): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284592 | |||||
chrX:284592
|
GCACACAC others(11): Show |
G | 1 | a0001c0001t0016g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127+283_127+300del others(18): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284592 | |||||
chrX:284600
|
GCACACAC others(3): Show |
G | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.127+291_127+300del others(10): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284600 | |||||
chrX:284602
|
ACACACGC others(15): Show |
A | 1 | a0001c0001t0034g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+299_127+320del others(22): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284602 | |||||
chrX:284629
|
C | T | 1 | a0001c0001t0034g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+315C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 284629 | ||||||
chrX:284638
|
GCA | G | 1 | a0001c0001t0027g0059 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127+333_127+334del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284638 | |||||
chrX:284640
|
A | G | 3 | a0001c0001t0005g0081a0001c0001t0005g0084a0001c0001t0078g0080 | 3 | NA18612.hp1 NA18950.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.127+326A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 284640 | ||||||
chrX:284658
|
GCA | G | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.127+353_127+354del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284658 | |||||
chrX:284775
|
T | TCA | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.127+462_127+463dup others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284775 | |||||
chrX:284809
|
CG | C | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127+497delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284809 | |||||
chrX:284982
|
TC | T | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127+671delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 284982 | |||||
chrX:285046
|
G | A | 17 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(14): Show | 17 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+732G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285046 | ||||||
chrX:285107
|
T | C | 2 | a0001c0001t0005g0038a0001c0001t0103g0037 | 2 | HG02080.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.127+793T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285107 | ||||||
chrX:285133
|
C | CAA | 1 | a0001c0001t0043g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.127+820_127+821ins others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285133 | |||||
chrX:285135
|
T | C | 1 | a0001c0001t0043g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.127+821T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285135 | ||||||
chrX:285135
|
T | TAAAC | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.127+822_127+823ins others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285135 | |||||
chrX:285268
|
G | A | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+954G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285268 | ||||||
chrX:285277
|
C | CTTCA | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127+964_127+965ins others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285277 | |||||
chrX:285279
|
C | A | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127+965C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285279 | ||||||
chrX:285298
|
A | AT | 1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.127+985dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285298 | |||||
chrX:285326
|
GTACACA | G | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+1014_127+1019d others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285326 | |||||
chrX:285341
|
CACACGTG others(1): Show |
C | 1 | a0001c0001t0017g0007 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+1032_127+1039d others(10): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285341 | |||||
chrX:285372
|
ATG | A | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+1060_127+1061d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285372 | |||||
chrX:285402
|
A | G | 1 | a0001c0001t0017g0007 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127+1088A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285402 | ||||||
chrX:285412
|
C | T | 1 | a0001c0001t0095g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+1098C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285412 | ||||||
chrX:285457
|
T | C | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127+1143T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285457 | ||||||
chrX:285539
|
GCA | G | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+1230_127+1231d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285539 | |||||
chrX:285556
|
T | A | 2 | a0001c0002t0039g0127a0001c0002t0105g0128 | 2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.127+1242T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285556 | ||||||
chrX:285558
|
T | TAC | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.127+1248_127+1249d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285558 | |||||
chrX:285619
|
G | A | 22 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0009g0075others(19): Show | 22 | HG00735.hp2 HG01123.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.127+1305G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285619 | ||||||
chrX:285619
|
GCA | G | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1310_127+1311d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285619 | |||||
chrX:285640
|
C | CGT | 1 | a0001c0001t0033g0078 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.127+1329_127+1330d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285640 | |||||
chrX:285660
|
C | T | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.127+1346C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285660 | ||||||
chrX:285664
|
GAC | G | 1 | a0001c0001t0034g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+1355_127+1356d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285664 | |||||
chrX:285670
|
C | T | 19 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.127+1356C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285670 | ||||||
chrX:285698
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+1384T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285698 | ||||||
chrX:285727
|
TCA | T | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1416_127+1417d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285727 | |||||
chrX:285772
|
T | C | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+1458T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285772 | ||||||
chrX:285790
|
ATAAACT | A | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1479_127+1484d others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285790 | |||||
chrX:285791
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.127+1477T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285791 | ||||||
chrX:285939
|
A | AG | 2 | a0001c0001t0027g0059a0001c0001t0113g0166 | 2 | NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.127+1630dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285939 | |||||
chrX:285939
|
AG | A | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127+1630delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 285939 | |||||
chrX:285996
|
C | T | 2 | a0001c0003t0058g0103a0001c0003t0088g0152 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.127+1682C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285996 | ||||||
chrX:285997
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.127+1683G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285997 | ||||||
chrX:286069
|
A | AT | 8 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+1767dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286069 | |||||
chrX:286069
|
AT | A | 2 | a0001c0003t0058g0103a0006c0020t0001g0111 | 2 | HG02622.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.127+1767delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286069 | |||||
chrX:286115
|
A | G | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+1801A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286115 | ||||||
chrX:286130
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.127+1816C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286130 | ||||||
chrX:286133
|
C | A | 1 | a0001c0001t0067g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.127+1819C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286133 | ||||||
chrX:286185
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.127+1871C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286185 | ||||||
chrX:286231
|
A | G | 16 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0009g0075others(13): Show | 16 | HG00735.hp2 HG01496.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.127+1917A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286231 | ||||||
chrX:286231
|
AT | A | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127+1922delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286231 | |||||
chrX:286248
|
A | T | 4 | a0001c0001t0004g0028a0001c0001t0041g0164a0001c0001t0045g0031others(1): Show | 4 | HG00438.hp2 HG00609.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+1934A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286248 | ||||||
chrX:286318
|
GC | G | 1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.127+2006delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286318 | |||||
chrX:286478
|
G | A | 8 | a0001c0001t0007g0121a0001c0001t0007g0124a0001c0001t0010g0122others(5): Show | 8 | HG02080.hp2 HG03669.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+2164G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286478 | ||||||
chrX:286517
|
G | A | 1 | a0001c0001t0028g0070 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.127+2203G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286517 | ||||||
chrX:286589
|
G | A | 27 | a0001c0001t0009g0065a0001c0001t0009g0067a0001c0001t0009g0075others(24): Show | 27 | HG00735.hp2 HG01123.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-2144G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286589 | ||||||
chrX:286638
|
G | A | 18 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(15): Show | 18 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.128-2095G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286638 | ||||||
chrX:286704
|
C | G | 1 | a0001c0001t0071g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.128-2029C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286704 | ||||||
chrX:286759
|
TC | T | 1 | a0001c0003t0082g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.128-1971delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286759 | |||||
chrX:286768
|
TG | T | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.128-1962delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286768 | |||||
chrX:286779
|
GC | G | 1 | a0001c0001t0114g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.128-1952delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 286779 | |||||
chrX:286944
|
G | C | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.128-1789G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286944 | ||||||
chrX:287081
|
T | A | 1 | a0001c0001t0016g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-1652T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287081 | ||||||
chrX:287172
|
T | TAC | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-1551_128-1550d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287172 | |||||
chrX:287172
|
TACAC | T | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-1553_128-1550d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287172 | |||||
chrX:287191
|
G | A | 6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0034g0069others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-1542G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287191 | ||||||
chrX:287233
|
A | G | 2 | a0001c0001t0086g0061a0001c0001t0087g0060 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.128-1500A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287233 | ||||||
chrX:287243
|
TATAA | T | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-1485_128-1482d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287243 | |||||
chrX:287259
|
T | TA | 1 | a0001c0002t0008g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.128-1470dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287259 | |||||
chrX:287334
|
CATA | C | 17 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(14): Show | 17 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-1395_128-1393d others(5): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287334 | |||||
chrX:287414
|
AAT | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-1314_128-1313d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287414 | |||||
chrX:287442
|
CACTATAT others(79): Show |
C | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-1268_128-1183d others(88): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287442 | |||||
chrX:287446
|
A | G | 17 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(14): Show | 17 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-1287A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287446 | ||||||
chrX:287468
|
T | TATACTAT others(22): Show |
1 | a0001c0002t0110g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.128-1102_128-1074d others(31): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287468 | |||||
chrX:287468
|
TATACTAT others(22): Show |
T | 5 | a0001c0001t0083g0085a0001c0002t0001g0154a0001c0002t0094g0140others(2): Show | 5 | HG00544.hp2 HG00733.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1102_128-1074d others(31): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287468 | |||||
chrX:287468
|
TATACTAT others(51): Show |
T | 16 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.128-1131_128-1074d others(60): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287468 | |||||
chrX:287468
|
TATACTAT others(80): Show |
T | 7 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0001t0086g0061others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1160_128-1074d others(89): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287468 | |||||
chrX:287492
|
AT | A | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128-1240delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287492 | ||||||
chrX:287497
|
G | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128-1236G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287497 | ||||||
chrX:287501
|
CTATATAT others(53): Show |
C | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.128-1226_128-1167d others(62): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287501 | |||||
chrX:287538
|
G | GT | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.128-1192dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287538 | |||||
chrX:287540
|
TTATATAT others(84): Show |
T | 2 | a0001c0003t0053g0162a0001c0003t0088g0152 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.128-1188_128-1098d others(93): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287540 | |||||
chrX:287553
|
T | C | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128-1180T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287553 | ||||||
chrX:287556
|
A | T | 1 | a0001c0002t0002g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-1177A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287556 | ||||||
chrX:287565
|
A | G | 6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0034g0069others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-1168A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287565 | ||||||
chrX:287567
|
GT | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-1163delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287567 | |||||
chrX:287569
|
TTATATAT others(55): Show |
T | 7 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(4): Show | 7 | HG02630.hp2 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-1159_128-1098d others(64): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287569 | |||||
chrX:287606
|
AGATATAG others(47): Show |
A | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.128-1108_128-1055d others(56): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287606 | |||||
chrX:287625
|
G | GTTTATAT others(23): Show |
1 | a0001c0002t0008g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.128-1105_128-1076d others(32): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287625 | |||||
chrX:287635
|
A | G | 9 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-1098A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287635 | ||||||
chrX:287635
|
AGATATAG others(18): Show |
A | 13 | a0001c0001t0001g0005a0001c0001t0007g0121a0001c0001t0007g0124others(10): Show | 14 | HG02080.hp2 HG02647.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-1079_128-1055d others(27): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287635 | |||||
chrX:287656
|
T | TTATATAT others(26): Show |
1 | a0001c0003t0044g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-1074_128-1073i others(35): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287656 | |||||
chrX:287660
|
G | A | 1 | a0001c0003t0044g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-1073G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287660 | ||||||
chrX:287672
|
T | TA | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-1060dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287672 | |||||
chrX:287679
|
C | G | 19 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0017g0007others(16): Show | 20 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.128-1054C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287679 | ||||||
chrX:287719
|
GAT | G | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.128-1009_128-1008d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287719 | |||||
chrX:287728
|
C | CATATATA others(8): Show |
1 | a0001c0001t0071g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.128-986_128-972dup others(15): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287728 | |||||
chrX:287728
|
CATATATA others(8): Show |
C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-986_128-972del others(15): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287728 | |||||
chrX:287779
|
AT | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-951delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287779 | |||||
chrX:287836
|
C | T | 1 | a0001c0001t0003g0027 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.128-897C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287836 | ||||||
chrX:287844
|
A | G | 2 | a0001c0001t0017g0007a0001c0002t0090g0151 | 3 | HG02886.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-889A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287844 | ||||||
chrX:287889
|
G | A | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.128-844G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287889 | ||||||
chrX:287898
|
CG | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-833delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287898 | |||||
chrX:287903
|
A | C | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.128-830A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287903 | ||||||
chrX:287944
|
T | TC | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-788dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 287944 | |||||
chrX:287973
|
C | T | 5 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(2): Show | 5 | HG02896.hp2 NA18941.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-760C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287973 | ||||||
chrX:287983
|
A | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-750A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287983 | ||||||
chrX:287984
|
G | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-749G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287984 | ||||||
chrX:287987
|
T | C | 1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-746T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287987 | ||||||
chrX:287989
|
T | C | 1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-744T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287989 | ||||||
chrX:287991
|
G | A | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.128-742G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287991 | ||||||
chrX:288022
|
TG | T | 1 | a0001c0001t0011g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128-706delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288022 | |||||
chrX:288032
|
AG | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-699delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288032 | |||||
chrX:288077
|
A | ATCTCCAC others(322): Show |
6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0034g0069others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-647_128-319dup others(329): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288077 | |||||
chrX:288099
|
TG | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-631delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288099 | |||||
chrX:288133
|
A | G | 2 | a0001c0002t0002g0108a0001c0002t0002g0139 | 2 | NA18945.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.128-600A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288133 | ||||||
chrX:288136
|
T | TA | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-596dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288136 | |||||
chrX:288148
|
CA | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-582delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288148 | |||||
chrX:288184
|
G | GAT | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-549_128-548ins others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288184 | ||||||
chrX:288234
|
G | GCAGGGGG others(322): Show |
2 | a0001c0001t0017g0007a0001c0002t0090g0151 | 3 | HG02886.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.128-328_128-327ins others(329): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288234 | |||||
chrX:288234
|
G | GCAGGGGG others(322): Show |
7 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0114g0013others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-319_128-318ins others(329): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288234 | |||||
chrX:288254
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.128-479C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288254 | ||||||
chrX:288259
|
CTT | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-471_128-470del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288259 | |||||
chrX:288283
|
AT | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-448delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288283 | |||||
chrX:288299
|
GT | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-432delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288299 | |||||
chrX:288321
|
TG | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-407delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288321 | |||||
chrX:288356
|
G | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-377G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288356 | ||||||
chrX:288357
|
C | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-376C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288357 | ||||||
chrX:288363
|
G | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-370G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288363 | ||||||
chrX:288370
|
T | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-363T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288370 | ||||||
chrX:288373
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.128-360G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288373 | ||||||
chrX:288389
|
C | G | 5 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(2): Show | 5 | HG02896.hp2 NA18941.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-344C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288389 | ||||||
chrX:288409
|
TC | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-322delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288409 | |||||
chrX:288421
|
C | T | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-312C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288421 | ||||||
chrX:288584
|
T | TG | 1 | a0001c0001t0099g0120 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.128-144dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288584 | |||||
chrX:288599
|
AC | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-130delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288599 | |||||
chrX:288633
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 64 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.128-100C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288633 | ||||||
chrX:288685
|
CG | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-44delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 288685 | |||||
chrX:288706
|
A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.128-27A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288706 | ||||||
chrX:288716
|
G | A | 6 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0114g0013others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-17G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288716 | ||||||
chrX:288925
|
GC | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+60delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 288925 | |||||
chrX:289027
|
A | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+158A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289027 | ||||||
chrX:289028
|
C | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+159C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289028 | ||||||
chrX:289029
|
A | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+160A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289029 | ||||||
chrX:289158
|
G | C | 3 | a0001c0001t0066g0161a0001c0003t0002g0159a0001c0003t0082g0160 | 3 | HG00408.hp2 NA18992.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.264+289G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289158 | ||||||
chrX:289174
|
G | A | 2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.264+305G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289174 | ||||||
chrX:289200
|
G | A | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.264+331G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289200 | ||||||
chrX:289248
|
T | TG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+381dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289248 | |||||
chrX:289254
|
A | T | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+385A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289254 | ||||||
chrX:289255
|
T | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+386T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289255 | ||||||
chrX:289337
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.264+468C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289337 | ||||||
chrX:289339
|
A | G | 1 | a0001c0001t0003g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.264+470A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289339 | ||||||
chrX:289367
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.264+498G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289367 | ||||||
chrX:289379
|
GC | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+513delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289379 | |||||
chrX:289391
|
AT | A | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.264+526delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289391 | |||||
chrX:289392
|
T | C | 9 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0003t0053g0162others(6): Show | 9 | HG01123.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.264+523T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289392 | ||||||
chrX:289428
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.264+559C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289428 | ||||||
chrX:289510
|
C | CTTT | 15 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(12): Show | 15 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.264+644_264+646dup others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289510 | |||||
chrX:289510
|
C | CTTTT | 2 | a0001c0001t0085g0090a0001c0001t0092g0089 | 2 | HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.264+643_264+646dup others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289510 | |||||
chrX:289516
|
C | CT | 17 | a0001c0001t0003g0029a0001c0001t0012g0015a0001c0001t0012g0149others(14): Show | 18 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.264+661dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289516 | |||||
chrX:289516
|
C | CTT | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.264+660_264+661dup others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289516 | |||||
chrX:289516
|
C | CTTT | 7 | a0001c0001t0003g0025a0001c0002t0097g0141a0001c0003t0053g0162others(4): Show | 7 | HG01123.hp2 HG02135.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+659_264+661dup others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289516 | |||||
chrX:289516
|
C | CTTTT | 1 | a0001c0003t0054g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.264+658_264+661dup others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289516 | |||||
chrX:289516
|
C | T | 17 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(14): Show | 17 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.264+647C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289516 | ||||||
chrX:289516
|
CTT | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+660_264+661del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289516 | |||||
chrX:289549
|
C | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.264+680C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289549 | ||||||
chrX:289580
|
C | T | 7 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0034g0069others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.264+711C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289580 | ||||||
chrX:289596
|
C | CT | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+727_264+728ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289596 | ||||||
chrX:289656
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.264+787C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289656 | ||||||
chrX:289663
|
G | C | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.264+794G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289663 | ||||||
chrX:289678
|
AT | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+814delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289678 | |||||
chrX:289687
|
AT | A | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.264+822delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289687 | |||||
chrX:289735
|
A | G | 9 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0034g0069others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+866A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289735 | ||||||
chrX:289742
|
A | AC | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+875dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289742 | |||||
chrX:289754
|
AC | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+888delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289754 | |||||
chrX:289767
|
T | TC | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-878dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289767 | |||||
chrX:289770
|
C | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-878C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289770 | ||||||
chrX:289790
|
C | T | 4 | a0001c0002t0039g0127a0001c0002t0105g0128a0003c0007t0019g0009others(1): Show | 4 | HG00544.hp1 HG00558.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-858C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289790 | ||||||
chrX:289793
|
C | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.265-855C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289793 | ||||||
chrX:289800
|
C | T | 2 | a0001c0001t0011g0125a0001c0001t0011g0126 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.265-848C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289800 | ||||||
chrX:289803
|
G | A | 20 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(17): Show | 21 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.265-845G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289803 | ||||||
chrX:289806
|
C | T | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.265-842C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289806 | ||||||
chrX:289837
|
C | G | 21 | a0001c0001t0001g0086a0001c0001t0005g0096a0001c0001t0010g0087others(18): Show | 22 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-811C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289837 | ||||||
chrX:289866
|
C | G | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.265-782C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289866 | ||||||
chrX:289910
|
C | G | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.265-738C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289910 | ||||||
chrX:289921
|
G | GA | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-724dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 289921 | |||||
chrX:289970
|
C | G | 7 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0034g0069others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-678C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289970 | ||||||
chrX:290038
|
GC | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-608delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290038 | |||||
chrX:290082
|
CG | C | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.265-563delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290082 | |||||
chrX:290095
|
C | G | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.265-553C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290095 | ||||||
chrX:290125
|
AT | A | 1 | a0001c0001t0050g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.265-518delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290125 | |||||
chrX:290140
|
A | C | 2 | a0001c0003t0051g0071a0001c0003t0058g0103 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.265-508A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290140 | ||||||
chrX:290153
|
C | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.265-495C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290153 | ||||||
chrX:290154
|
G | A | 2 | a0001c0001t0011g0125a0001c0001t0011g0126 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.265-494G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290154 | ||||||
chrX:290155
|
C | T | 2 | a0001c0001t0011g0125a0001c0001t0011g0126 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.265-493C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290155 | ||||||
chrX:290163
|
C | T | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.265-485C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290163 | ||||||
chrX:290165
|
C | T | 2 | a0001c0002t0093g0137a0001c0002t0098g0136 | 2 | HG00738.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.265-483C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290165 | ||||||
chrX:290166
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.265-482G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290166 | ||||||
chrX:290172
|
A | AAT | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-475_265-474dup others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290172 | |||||
chrX:290202
|
T | C | 1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.265-446T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290202 | ||||||
chrX:290210
|
G | A | 28 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0015g0073others(25): Show | 29 | HG01123.hp2 HG01168.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.265-438G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290210 | ||||||
chrX:290221
|
A | T | 2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.265-427A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290221 | ||||||
chrX:290238
|
T | C | 11 | a0001c0001t0017g0007a0001c0001t0018g0099a0001c0001t0018g0100others(8): Show | 12 | HG02257.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.265-410T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290238 | ||||||
chrX:290243
|
T | C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.265-405T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290243 | ||||||
chrX:290244
|
G | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.265-404G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290244 | ||||||
chrX:290245
|
T | G | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.265-403T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290245 | ||||||
chrX:290253
|
A | C | 5 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0014g0048others(2): Show | 5 | HG00099.hp2 HG00735.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-395A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290253 | ||||||
chrX:290255
|
A | G | 5 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0014g0048others(2): Show | 5 | HG00099.hp2 HG00735.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-393A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290255 | ||||||
chrX:290263
|
T | TA | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-380dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290263 | |||||
chrX:290290
|
C | T | 19 | a0001c0001t0005g0081a0001c0001t0005g0084a0001c0001t0007g0121others(16): Show | 19 | HG00639.hp1 HG01123.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-358C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290290 | ||||||
chrX:290292
|
C | CG | 1 | a0001c0002t0039g0127 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.265-354dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290292 | |||||
chrX:290298
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.265-350C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290298 | ||||||
chrX:290302
|
C | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.265-346C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290302 | ||||||
chrX:290314
|
C | T | 6 | a0001c0002t0002g0142a0001c0003t0002g0016a0001c0003t0020g0036others(3): Show | 6 | HG01070.hp2 HG01109.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-334C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290314 | ||||||
chrX:290325
|
G | C | 2 | a0001c0001t0005g0038a0001c0001t0103g0037 | 2 | HG02080.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.265-323G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290325 | ||||||
chrX:290343
|
C | T | 34 | a0001c0001t0005g0081a0001c0001t0005g0084a0001c0001t0007g0121others(31): Show | 35 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.265-305C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290343 | ||||||
chrX:290347
|
A | G | 11 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0018g0099others(8): Show | 11 | HG00639.hp1 HG01123.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-301A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290347 | ||||||
chrX:290358
|
A | AG | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-288dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290358 | |||||
chrX:290361
|
C | CG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-285dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290361 | |||||
chrX:290392
|
T | C | 1 | a0001c0002t0064g0156 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.265-256T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290392 | ||||||
chrX:290407
|
G | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.265-241G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290407 | ||||||
chrX:290408
|
T | C | 2 | a0001c0001t0011g0125a0001c0001t0011g0126 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.265-240T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290408 | ||||||
chrX:290408
|
T | TG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-239dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290408 | |||||
chrX:290417
|
G | A | 3 | a0001c0001t0012g0015a0001c0001t0012g0149a0010c0008t0077g0072 | 3 | HG02723.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.265-231G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290417 | ||||||
chrX:290424
|
C | T | 14 | a0001c0001t0005g0081a0001c0001t0005g0084a0001c0001t0007g0121others(11): Show | 14 | HG02080.hp2 HG02922.hp1 HG03139.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-224C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290424 | ||||||
chrX:290429
|
C | CA | 4 | a0001c0001t0034g0069a0001c0002t0019g0130a0001c0002t0039g0127others(1): Show | 4 | HG03486.hp1 NA18972.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-203dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290429 | |||||
chrX:290429
|
CA | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.265-203delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290429 | |||||
chrX:290429
|
CAA | C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.265-204_265-203del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290429 | |||||
chrX:290448
|
C | T | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-200C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290448 | ||||||
chrX:290532
|
C | CA | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-115dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290532 | |||||
chrX:290538
|
C | T | 1 | a0001c0002t0002g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.265-110C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290538 | ||||||
chrX:290539
|
G | A | 14 | a0001c0002t0090g0151a0001c0003t0002g0018a0001c0003t0002g0044others(11): Show | 14 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-109G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290539 | ||||||
chrX:290570
|
C | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-78C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290570 | ||||||
chrX:290572
|
A | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-76A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290572 | ||||||
chrX:290574
|
C | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-74C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290574 | ||||||
chrX:290592
|
A | AG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-55dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290592 | |||||
chrX:290593
|
G | GC | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-49dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290593 | |||||
chrX:290605
|
C | CG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-41dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 290605 | |||||
chrX:290784
|
C | T | 55 | a0001c0001t0001g0086a0001c0001t0005g0038a0001c0001t0005g0096others(52): Show | 56 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(53): Show |
splice_region_variant&intron_variant | LOW | c.393+8C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290784 | ||||||
chrX:290802
|
A | G | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+26A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290802 | ||||||
chrX:290804
|
T | G | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+28T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290804 | ||||||
chrX:290811
|
AG | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.393+36delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290811 | ||||||
chrX:290813
|
TGGGAGGC others(55): Show |
T | 8 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0086g0061others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+115_393+176del others(62): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290813 | |||||
chrX:290813
|
TGGGAGGC others(117): Show |
T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.393+53_393+176del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290813 | |||||
chrX:290821
|
G | A | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.393+45G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290821 | ||||||
chrX:290824
|
C | T | 1 | a0001c0003t0065g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.393+48C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290824 | ||||||
chrX:290825
|
G | A | 2 | a0001c0003t0002g0018a0001c0003t0002g0044 | 2 | HG01168.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.393+49G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290825 | ||||||
chrX:290829
|
ACTGGTGC others(117): Show |
A | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.393+97_393+220del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290829 | |||||
chrX:290861
|
A | C | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+85A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290861 | ||||||
chrX:290866
|
G | T | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+90G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290866 | ||||||
chrX:290872
|
C | G | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+96C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290872 | ||||||
chrX:290873
|
A | G | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+97A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290873 | ||||||
chrX:290875
|
C | T | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+99C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290875 | ||||||
chrX:290875
|
CG | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.393+102delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290875 | |||||
chrX:290882
|
CGGCCGGG others(117): Show |
C | 1 | a0010c0008t0077g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.393+111_393+234del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290882 | |||||
chrX:290883
|
G | A | 1 | a0001c0001t0017g0007 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.393+107G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290883 | ||||||
chrX:290886
|
C | CGGGCGCT others(179): Show |
2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.393+114_393+115ins others(186): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290886 | |||||
chrX:290891
|
A | G | 4 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0003t0053g0162others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+115A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290891 | ||||||
chrX:290906
|
G | GGC | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.393+130_393+131ins others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290906 | ||||||
chrX:290908
|
C | G | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.393+132C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290908 | ||||||
chrX:290908
|
C | T | 8 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+132C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290908 | ||||||
chrX:290923
|
A | C | 9 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(6): Show | 9 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+147A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290923 | ||||||
chrX:290924
|
G | A | 1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+148G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290924 | ||||||
chrX:290928
|
G | T | 9 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(6): Show | 9 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+152G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290928 | ||||||
chrX:290934
|
C | G | 8 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+158C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290934 | ||||||
chrX:290937
|
C | T | 8 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+161C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290937 | ||||||
chrX:290951
|
G | A | 4 | a0001c0004t0007g0106a0001c0004t0007g0110a0001c0004t0112g0105others(1): Show | 4 | NA18942.hp2 NA18947.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+175G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290951 | ||||||
chrX:290953
|
G | A | 8 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0025g0079others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+177G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290953 | ||||||
chrX:290953
|
G | GCTGGTGC others(55): Show |
2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.393+193_393+194ins others(62): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290953 | |||||
chrX:290966
|
C | CG | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.393+192dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 290966 | |||||
chrX:290997
|
G | A | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.393+221G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290997 | ||||||
chrX:291006
|
T | C | 4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0005t0106g0077others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+230T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291006 | ||||||
chrX:291019
|
G | T | 2 | a0001c0001t0011g0125a0001c0001t0011g0126 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.393+243G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291019 | ||||||
chrX:291057
|
A | G | 14 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0003t0006g0041others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+281A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291057 | ||||||
chrX:291084
|
G | A | 4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0005t0106g0077others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+308G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291084 | ||||||
chrX:291139
|
C | CT | 6 | a0001c0001t0029g0019a0001c0002t0039g0127a0001c0003t0006g0041others(3): Show | 6 | HG01891.hp1 HG02056.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-350dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 291139 | |||||
chrX:291151
|
C | CT | 4 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0029others(1): Show | 4 | HG02135.hp2 NA18955.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-337dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 291151 | |||||
chrX:291151
|
CT | C | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.394-337delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 291151 | |||||
chrX:291180
|
G | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.394-319G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291180 | ||||||
chrX:291312
|
AT | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.394-182delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 291312 | |||||
chrX:291331
|
A | G | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.394-168A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291331 | ||||||
chrX:291374
|
A | G | 10 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0003t0006g0041others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-125A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291374 | ||||||
chrX:291385
|
ATC | A | 1 | a0006c0020t0001g0111 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.394-113_394-112del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291385 | ||||||
chrX:291398
|
G | A | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.394-101G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 291398 | ||||||
chrX:291438
|
A | AC | 1 | a0001c0002t0019g0130 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.394-57dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 291438 | |||||
chrX:291719
|
A | G | 28 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0018g0099others(25): Show | 28 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.549+65A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291719 | ||||||
chrX:291767
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 57 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.549+113G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291767 | ||||||
chrX:291780
|
G | A | 1 | a0001c0003t0081g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.549+126G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291780 | ||||||
chrX:291796
|
C | CA | 1 | a0004c0017t0040g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.549+142_549+143ins others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291796 | ||||||
chrX:291805
|
T | TG | 1 | a0001c0002t0004g0146 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.549+157dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 291805 | |||||
chrX:291889
|
C | CG | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.549+238dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 291889 | |||||
chrX:291997
|
G | C | 29 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0015g0073others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.549+343G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291997 | ||||||
chrX:292039
|
C | T | 7 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0003t0023g0020others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+385C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292039 | ||||||
chrX:292131
|
C | A | 1 | a0001c0001t0083g0085 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.549+477C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292131 | ||||||
chrX:292271
|
C | A | 1 | a0001c0002t0094g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.549+617C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292271 | ||||||
chrX:292271
|
C | T | 19 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0002t0090g0151others(16): Show | 19 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+617C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292271 | ||||||
chrX:292298
|
A | G | 1 | a0001c0002t0097g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.549+644A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292298 | ||||||
chrX:292315
|
C | T | 4 | a0001c0001t0018g0100a0001c0003t0055g0010a0001c0003t0058g0103others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+661C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292315 | ||||||
chrX:292319
|
C | T | 1 | a0005c0015t0109g0113 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.549+665C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292319 | ||||||
chrX:292321
|
T | A | 4 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(1): Show | 4 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+667T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292321 | ||||||
chrX:292327
|
C | T | 1 | a0005c0015t0109g0113 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.549+673C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292327 | ||||||
chrX:292351
|
C | T | 2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.550-684C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292351 | ||||||
chrX:292383
|
C | T | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.550-652C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292383 | ||||||
chrX:292409
|
A | T | 1 | a0001c0001t0041g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.550-626A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292409 | ||||||
chrX:292416
|
G | A | 1 | a0001c0001t0010g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.550-619G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292416 | ||||||
chrX:292425
|
T | C | 1 | a0001c0001t0003g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.550-610T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292425 | ||||||
chrX:292431
|
C | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.550-604C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292431 | ||||||
chrX:292446
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.550-589G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292446 | ||||||
chrX:292447
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.550-588A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292447 | ||||||
chrX:292471
|
T | TA | 1 | a0001c0002t0039g0127 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.550-559dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 292471 | |||||
chrX:292495
|
T | C | 2 | a0001c0001t0012g0015a0001c0001t0012g0149 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.550-540T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292495 | ||||||
chrX:292651
|
C | T | 2 | a0001c0003t0055g0010a0001c0003t0089g0011 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.550-384C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292651 | ||||||
chrX:292680
|
T | A | 1 | a0010c0008t0077g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.550-355T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292680 | ||||||
chrX:292776
|
C | A | 1 | a0001c0001t0103g0037 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.550-259C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292776 | ||||||
chrX:292818
|
G | GC | 1 | a0001c0001t0029g0019 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.550-214dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 292818 | |||||
chrX:292886
|
T | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.550-149T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292886 | ||||||
chrX:292909
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.550-126G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292909 | ||||||
chrX:292971
|
C | T | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550-64C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292971 | ||||||
chrX:292985
|
C | T | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550-50C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292985 | ||||||
chrX:293229
|
G | A | 2 | a0003c0007t0019g0009a0003c0007t0021g0009 | 2 | HG00544.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.733+11G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293229 | ||||||
chrX:293274
|
C | T | 12 | a0001c0002t0090g0151a0001c0003t0002g0018a0001c0003t0002g0044others(9): Show | 12 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.733+56C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293274 | ||||||
chrX:293291
|
A | G | 2 | a0001c0002t0002g0135a0011c0016t0006g0076 | 2 | HG00733.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.733+73A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293291 | ||||||
chrX:293335
|
C | A | 1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.733+117C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293335 | ||||||
chrX:293369
|
A | T | 1 | a0001c0002t0038g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.733+151A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293369 | ||||||
chrX:293381
|
C | T | 1 | a0001c0001t0050g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.733+163C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293381 | ||||||
chrX:293394
|
C | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.733+176C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293394 | ||||||
chrX:293605
|
C | A | 1 | a0001c0001t0092g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.733+387C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293605 | ||||||
chrX:293645
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.733+427G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293645 | ||||||
chrX:293766
|
C | T | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.733+548C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293766 | ||||||
chrX:293782
|
C | T | 2 | a0001c0003t0054g0094a0001c0003t0056g0092 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.733+564C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 293782 | ||||||
chrX:294005
|
G | C | 1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733+787G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294005 | ||||||
chrX:294065
|
G | A | 35 | a0001c0001t0001g0086a0001c0001t0005g0038a0001c0001t0005g0081others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.733+847G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294065 | ||||||
chrX:294116
|
C | T | 1 | a0001c0001t0071g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.733+898C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294116 | ||||||
chrX:294209
|
G | A | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+991G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294209 | ||||||
chrX:294227
|
A | C | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+1009A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294227 | ||||||
chrX:294241
|
G | A | 1 | a0001c0004t0007g0110 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.733+1023G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294241 | ||||||
chrX:294253
|
C | T | 14 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0029g0019others(11): Show | 14 | HG01891.hp1 HG02056.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.733+1035C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294253 | ||||||
chrX:294257
|
C | T | 2 | a0001c0003t0051g0071a0001c0003t0058g0103 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.733+1039C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294257 | ||||||
chrX:294263
|
A | G | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+1045A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294263 | ||||||
chrX:294264
|
T | C | 3 | a0001c0001t0050g0043a0001c0003t0051g0071a0001c0003t0058g0103 | 3 | HG02615.hp2 HG02622.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.733+1046T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294264 | ||||||
chrX:294273
|
G | A | 2 | a0001c0003t0051g0071a0001c0003t0058g0103 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.733+1055G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294273 | ||||||
chrX:294278
|
C | T | 2 | a0001c0003t0051g0071a0001c0003t0058g0103 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.733+1060C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294278 | ||||||
chrX:294289
|
C | T | 8 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+1071C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294289 | ||||||
chrX:294354
|
C | T | 2 | a0001c0002t0090g0151a0001c0003t0089g0011 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.733+1136C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294354 | ||||||
chrX:294362
|
A | G | 2 | a0001c0002t0002g0134a0001c0002t0002g0135 | 2 | HG00733.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.733+1144A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294362 | ||||||
chrX:294384
|
A | G | 1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733+1166A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294384 | ||||||
chrX:294387
|
T | C | 4 | a0001c0001t0025g0079a0001c0001t0027g0059a0001c0001t0033g0078others(1): Show | 4 | NA18941.hp1 NA18964.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+1169T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294387 | ||||||
chrX:294388
|
A | G | 1 | a0001c0001t0009g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.733+1170A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294388 | ||||||
chrX:294454
|
C | T | 1 | a0001c0003t0088g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.733+1236C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294454 | ||||||
chrX:294481
|
C | CA | 2 | a0001c0001t0001g0158a0001c0002t0098g0136 | 2 | HG00323.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.733+1279dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 294481 | |||||
chrX:294481
|
C | CAA | 1 | a0010c0008t0077g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.733+1278_733+1279d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 294481 | |||||
chrX:294481
|
CA | C | 15 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0074g0143others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.733+1279delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 294481 | |||||
chrX:294491
|
A | G | 10 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0003t0006g0041others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+1273A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294491 | ||||||
chrX:294609
|
G | A | 3 | a0000c0018t0101g0132a0001c0002t0008g0117a0001c0002t0008g0131 | 3 | HG01993.hp1 HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.733+1391G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294609 | ||||||
chrX:294758
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.733+1540C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294758 | ||||||
chrX:294780
|
G | C | 7 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0051g0071others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+1562G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294780 | ||||||
chrX:294824
|
CA | C | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+1609delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 294824 | |||||
chrX:294870
|
G | A | 13 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0015others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.733+1652G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294870 | ||||||
chrX:294894
|
A | G | 2 | a0001c0003t0002g0018a0001c0003t0002g0044 | 2 | HG01168.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.733+1676A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294894 | ||||||
chrX:294982
|
T | TC | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+1765dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 294982 | |||||
chrX:295049
|
A | G | 31 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0015others(28): Show | 31 | HG00544.hp2 HG00738.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.733+1831A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295049 | ||||||
chrX:295051
|
TC | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+1836delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295051 | |||||
chrX:295063
|
G | A | 5 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+1845G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295063 | ||||||
chrX:295171
|
G | GA | 4 | a0001c0001t0016g0082a0001c0001t0092g0089a0001c0002t0002g0135others(1): Show | 4 | HG00733.hp1 HG04184.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+1966dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295171 | |||||
chrX:295171
|
G | GC | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+1953_733+1954i others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295171 | ||||||
chrX:295171
|
GA | G | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.733+1966delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295171 | |||||
chrX:295222
|
G | GTA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2005_733+2006d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295222 | |||||
chrX:295238
|
C | CG | 2 | a0001c0001t0029g0019a0001c0002t0105g0128 | 2 | HG02056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.733+2024dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295238 | |||||
chrX:295256
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2039dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295256 | |||||
chrX:295257
|
A | G | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.733+2039A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295257 | ||||||
chrX:295306
|
A | AG | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2091dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295306 | |||||
chrX:295330
|
C | T | 2 | a0001c0001t0086g0061a0001c0001t0087g0060 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.733+2112C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295330 | ||||||
chrX:295336
|
C | CG | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2120dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295336 | |||||
chrX:295353
|
G | A | 1 | a0009c0013t0021g0150 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.733+2135G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295353 | ||||||
chrX:295401
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.733+2183G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295401 | ||||||
chrX:295402
|
G | GC | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2186dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295402 | |||||
chrX:295406
|
C | T | 1 | a0001c0002t0049g0023 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.733+2188C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295406 | ||||||
chrX:295458
|
A | G | 35 | a0001c0001t0007g0121a0001c0001t0007g0124a0001c0001t0011g0125others(32): Show | 35 | HG01123.hp1 HG01346.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.733+2240A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295458 | ||||||
chrX:295487
|
G | A | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+2269G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295487 | ||||||
chrX:295503
|
G | A | 1 | a0001c0001t0043g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.733+2285G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295503 | ||||||
chrX:295506
|
GT | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 86 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.733+2291delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295506 | |||||
chrX:295527
|
C | CT | 4 | a0001c0001t0003g0025a0001c0001t0059g0123a0001c0001t0078g0080others(1): Show | 4 | HG02135.hp2 NA18950.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2323dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295527 | |||||
chrX:295527
|
CT | C | 26 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0018g0099others(23): Show | 26 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.733+2323delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295527 | |||||
chrX:295545
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.733+2327G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295545 | ||||||
chrX:295566
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2348_733+2349i others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295566 | ||||||
chrX:295568
|
C | CG | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.733+2352dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295568 | |||||
chrX:295586
|
G | A | 2 | a0001c0003t0044g0115a0001c0003t0088g0152 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.733+2368G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295586 | ||||||
chrX:295617
|
C | T | 16 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0016g0082others(13): Show | 16 | HG01346.hp2 HG01891.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.733+2399C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295617 | ||||||
chrX:295670
|
G | A | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+2452G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295670 | ||||||
chrX:295674
|
G | A | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+2456G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295674 | ||||||
chrX:295682
|
AC | A | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2467delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295682 | |||||
chrX:295718
|
A | G | 18 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0018g0099others(15): Show | 18 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.733+2500A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295718 | ||||||
chrX:295731
|
G | GT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2515dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295731 | |||||
chrX:295737
|
C | T | 3 | a0001c0001t0086g0061a0001c0001t0087g0060a0001c0002t0105g0128 | 3 | HG01891.hp2 HG03516.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.733+2519C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295737 | ||||||
chrX:295821
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2604dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295821 | |||||
chrX:295831
|
A | AT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2620dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295831 | |||||
chrX:295851
|
G | GT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2639dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295851 | |||||
chrX:295918
|
G | GC | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2701dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295918 | |||||
chrX:295927
|
G | A | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.733+2709G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295927 | ||||||
chrX:295936
|
G | GT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2720dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295936 | |||||
chrX:295945
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.733+2727A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295945 | ||||||
chrX:295951
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2733_733+2734i others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295951 | ||||||
chrX:295955
|
C | T | 13 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0027g0059others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.733+2737C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295955 | ||||||
chrX:295975
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.733+2757G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295975 | ||||||
chrX:295980
|
A | ATTT | 7 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+2765_733+2767d others(5): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 295980 | |||||
chrX:296035
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.733+2817C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296035 | ||||||
chrX:296040
|
G | A | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0114g0013 | 3 | HG02280.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.733+2822G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296040 | ||||||
chrX:296046
|
A | AG | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2830dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296046 | |||||
chrX:296075
|
G | C | 6 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+2857G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296075 | ||||||
chrX:296092
|
T | A | 6 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+2874T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296092 | ||||||
chrX:296103
|
T | C | 6 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+2885T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296103 | ||||||
chrX:296104
|
G | A | 6 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+2886G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296104 | ||||||
chrX:296117
|
T | TTTG | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.733+2900_733+2901i others(5): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296117 | |||||
chrX:296122
|
T | A | 1 | a0001c0001t0016g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.733+2904T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296122 | ||||||
chrX:296155
|
C | G | 7 | a0001c0003t0002g0018a0001c0003t0002g0044a0001c0003t0065g0012others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+2937C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296155 | ||||||
chrX:296261
|
C | CT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2836_734-2835i others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296261 | ||||||
chrX:296279
|
C | A | 1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-2818C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296279 | ||||||
chrX:296279
|
C | CCT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2818_734-2817i others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296279 | ||||||
chrX:296280
|
T | A | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2817T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296280 | ||||||
chrX:296297
|
G | A | 19 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0015g0073others(16): Show | 20 | HG01346.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.734-2800G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296297 | ||||||
chrX:296311
|
G | A | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2786G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296311 | ||||||
chrX:296312
|
A | G | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2785A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296312 | ||||||
chrX:296315
|
G | T | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-2782G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296315 | ||||||
chrX:296317
|
G | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2780G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296317 | ||||||
chrX:296358
|
C | CAG | 5 | a0001c0003t0065g0012a0001c0003t0107g0104a0002c0005t0022g0035others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-2738_734-2737i others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296358 | |||||
chrX:296363
|
TC | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2732delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296363 | |||||
chrX:296369
|
G | A | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-2728G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296369 | ||||||
chrX:296390
|
TG | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2704delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296390 | |||||
chrX:296398
|
C | T | 1 | a0001c0001t0059g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.734-2699C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296398 | ||||||
chrX:296425
|
GA | G | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2669delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296425 | |||||
chrX:296433
|
T | G | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2664T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296433 | ||||||
chrX:296446
|
T | C | 1 | a0001c0001t0027g0059 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.734-2651T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296446 | ||||||
chrX:296449
|
G | A | 21 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0016g0082others(18): Show | 22 | HG01346.hp2 HG01891.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-2648G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296449 | ||||||
chrX:296475
|
C | A | 5 | a0001c0003t0065g0012a0001c0003t0107g0104a0002c0005t0022g0035others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-2622C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296475 | ||||||
chrX:296492
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.734-2605T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296492 | ||||||
chrX:296519
|
AG | A | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2574delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296519 | |||||
chrX:296536
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2561_734-2560i others(3): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296536 | ||||||
chrX:296539
|
C | CT | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2557dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296539 | |||||
chrX:296560
|
T | C | 8 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0003t0065g0012others(5): Show | 8 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-2537T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296560 | ||||||
chrX:296607
|
A | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2490A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296607 | ||||||
chrX:296612
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2484dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296612 | |||||
chrX:296635
|
C | CCA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2460_734-2459d others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296635 | |||||
chrX:296635
|
C | T | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-2462C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296635 | ||||||
chrX:296663
|
A | AC | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2431dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296663 | |||||
chrX:296725
|
CCTGT | C | 1 | a0001c0001t0032g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.734-2369_734-2366d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296725 | |||||
chrX:296759
|
A | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.734-2338A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296759 | ||||||
chrX:296771
|
T | TATTATTC others(188): Show |
1 | a0001c0001t0048g0030 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.734-2182_734-2181i others(197): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296771 | |||||
chrX:296780
|
G | GT | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2316dupT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296780 | |||||
chrX:296790
|
TG | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2304delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296790 | |||||
chrX:296832
|
A | G | 24 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(21): Show | 25 | HG01123.hp1 HG01346.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.734-2265A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296832 | ||||||
chrX:296842
|
G | GA | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2254dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296842 | |||||
chrX:296856
|
C | CATCTTTG others(532): Show |
3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-2217_734-2216i others(541): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296856 | |||||
chrX:296867
|
A | ACATTAAT others(238): Show |
3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-2225_734-2224i others(247): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296867 | |||||
chrX:296880
|
T | TCCCACAT others(42): Show |
6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0027g0059others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-2182_734-2181i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296880 | |||||
chrX:296881
|
C | A | 4 | a0001c0003t0107g0104a0002c0005t0022g0035a0002c0005t0106g0077others(1): Show | 4 | HG00639.hp1 HG00735.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-2216C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296881 | ||||||
chrX:296882
|
C | CCACATGG others(432): Show |
1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.734-2182_734-2181i others(441): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296882 | |||||
chrX:296882
|
C | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-2215C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296882 | ||||||
chrX:296882
|
CCACATGG others(42): Show |
C | 1 | a0001c0001t0043g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.734-2181_734-2133d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296882 | |||||
chrX:296884
|
A | ACATGGGG others(188): Show |
1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-2182_734-2181i others(197): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296884 | |||||
chrX:296884
|
A | ACATGGGG others(530): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-2182_734-2181i others(539): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296884 | |||||
chrX:296884
|
A | ACATGGGG others(334): Show |
8 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-2182_734-2181i others(343): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296884 | |||||
chrX:296884
|
A | ACATGGGG others(335): Show |
1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-2175_734-2174i others(344): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296884 | |||||
chrX:296884
|
A | G | 1 | a0001c0002t0002g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.734-2213A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296884 | ||||||
chrX:296884
|
A | T | 3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-2213A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296884 | ||||||
chrX:296888
|
G | T | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2209G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296888 | ||||||
chrX:296894
|
T | C | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-2203T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296894 | ||||||
chrX:296916
|
C | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.734-2181C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296916 | ||||||
chrX:296916
|
C | CCATTATT others(91): Show |
1 | a0001c0002t0098g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.734-2168_734-2167i others(100): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296916 | |||||
chrX:296923
|
T | TC | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2173dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296923 | |||||
chrX:296929
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.734-2168T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296929 | ||||||
chrX:296930
|
A | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.734-2167A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296930 | ||||||
chrX:296931
|
T | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.734-2166T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296931 | ||||||
chrX:296931
|
T | TCACATGG others(42): Show |
1 | a0001c0002t0093g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.734-2119_734-2118i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296931 | |||||
chrX:296933
|
A | T | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-2164A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296933 | ||||||
chrX:296940
|
G | A | 3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-2157G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296940 | ||||||
chrX:296948
|
C | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-2149C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296948 | ||||||
chrX:296949
|
G | A | 1 | a0001c0001t0083g0085 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.734-2148G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296949 | ||||||
chrX:296965
|
A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.734-2132A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296965 | ||||||
chrX:296965
|
ACATTATT others(385): Show |
A | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-2118_734-1727d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296965 | |||||
chrX:296972
|
T | C | 1 | a0001c0001t0010g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.734-2125T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296972 | ||||||
chrX:296975
|
G | A | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-2122G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296975 | ||||||
chrX:296978
|
T | C | 21 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(18): Show | 22 | HG01123.hp1 HG01346.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-2119T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296978 | ||||||
chrX:296979
|
A | C | 32 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0015others(29): Show | 33 | HG01123.hp1 HG01123.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.734-2118A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296979 | ||||||
chrX:296980
|
T | C | 35 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0015others(32): Show | 36 | HG00639.hp1 HG00735.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.734-2117T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296980 | ||||||
chrX:296982
|
A | ACATGGGG others(90): Show |
1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-2077_734-2076i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296982 | |||||
chrX:296982
|
A | T | 3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-2115A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296982 | ||||||
chrX:296985
|
TG | T | 6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0027g0059others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-2108delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 296985 | |||||
chrX:296989
|
G | A | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-2108G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296989 | ||||||
chrX:297014
|
A | C | 29 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0015others(26): Show | 30 | HG01123.hp1 HG01123.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.734-2083A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297014 | ||||||
chrX:297020
|
TC | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2075delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297020 | |||||
chrX:297020
|
TCCTG | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-2076_734-2073d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297020 | ||||||
chrX:297021
|
C | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.734-2076C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297021 | ||||||
chrX:297026
|
C | G | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-2071C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297026 | ||||||
chrX:297028
|
A | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.734-2069A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297028 | ||||||
chrX:297029
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.734-2068T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297029 | ||||||
chrX:297029
|
T | TC | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-2067dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297029 | |||||
chrX:297031
|
A | T | 6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0027g0059others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-2066A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297031 | ||||||
chrX:297033
|
A | T | 6 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0027g0059others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-2064A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297033 | ||||||
chrX:297034
|
TG | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.734-2059delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297034 | |||||
chrX:297034
|
TGGGGATT others(92): Show |
T | 3 | a0001c0001t0057g0055a0001c0001t0074g0143a0001c0003t0060g0051 | 3 | HG01168.hp2 NA18992.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.734-2059_734-1961d others(101): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297034 | |||||
chrX:297046
|
C | T | 10 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0006g0041others(7): Show | 10 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-2051C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297046 | ||||||
chrX:297063
|
A | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.734-2034A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297063 | ||||||
chrX:297068
|
A | G | 1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.734-2029A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297068 | ||||||
chrX:297070
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.734-2027T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297070 | ||||||
chrX:297076
|
T | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0002t0090g0151 | 3 | HG02622.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.734-2021T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297076 | ||||||
chrX:297077
|
C | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.734-2020C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297077 | ||||||
chrX:297078
|
C | T | 10 | a0000c0018t0101g0132a0001c0003t0006g0041a0001c0003t0006g0042others(7): Show | 10 | HG01891.hp1 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-2019C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297078 | ||||||
chrX:297080
|
A | ACATGGGA others(41): Show |
1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-2011_734-2010i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297080 | |||||
chrX:297080
|
A | ACATGGGA others(90): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-2011_734-2010i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297080 | |||||
chrX:297080
|
A | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.734-2017A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297080 | ||||||
chrX:297082
|
A | ATGGGATT others(41): Show |
4 | a0001c0001t0012g0015a0001c0001t0027g0059a0001c0001t0052g0068others(1): Show | 4 | HG02257.hp2 HG02976.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2011_734-2010i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297082 | |||||
chrX:297083
|
TG | T | 19 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(16): Show | 20 | HG01123.hp1 HG01346.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.734-2010delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297083 | |||||
chrX:297090
|
C | T | 110 | a0000c0018t0101g0132a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.734-2007C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297090 | ||||||
chrX:297112
|
A | ACATTATT others(140): Show |
1 | a0001c0002t0094g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.734-1874_734-1873i others(149): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297112 | |||||
chrX:297112
|
A | C | 33 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0012g0149others(30): Show | 34 | HG01123.hp1 HG01123.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.734-1985A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297112 | ||||||
chrX:297115
|
T | A | 1 | a0001c0002t0008g0131 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.734-1982T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297115 | ||||||
chrX:297119
|
T | C | 19 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(16): Show | 20 | HG01123.hp1 HG01346.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.734-1978T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297119 | ||||||
chrX:297119
|
T | TCTGTCTA others(287): Show |
1 | a0001c0001t0010g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.734-1959_734-1958i others(296): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297119 | |||||
chrX:297127
|
T | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.734-1970T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297127 | ||||||
chrX:297129
|
A | ACATGGGG others(91): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1957_734-1956i others(100): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297129 | |||||
chrX:297129
|
A | ACATGGGG others(139): Show |
1 | a0001c0001t0018g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.734-1937_734-1936i others(148): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297129 | |||||
chrX:297129
|
A | ACATGGGG others(139): Show |
1 | a0001c0001t0018g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.734-1937_734-1936i others(148): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297129 | |||||
chrX:297129
|
A | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.734-1968A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297129 | ||||||
chrX:297133
|
G | GGGGATTA others(41): Show |
1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1937_734-1936i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297133 | |||||
chrX:297139
|
T | C | 1 | a0001c0001t0045g0031 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.734-1958T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297139 | ||||||
chrX:297146
|
T | TG | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-1949dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297146 | |||||
chrX:297161
|
C | A | 83 | a0000c0018t0101g0132a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.734-1936C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297161 | ||||||
chrX:297161
|
CCATTATT others(42): Show |
C | 1 | a0001c0001t0095g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.734-1860_734-1812d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297161 | |||||
chrX:297166
|
A | G | 8 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-1931A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297166 | ||||||
chrX:297167
|
TTCTG | T | 1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.734-1926_734-1923d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297167 | |||||
chrX:297168
|
T | C | 4 | a0001c0001t0057g0055a0001c0001t0074g0143a0001c0002t0090g0151others(1): Show | 4 | HG01168.hp2 HG02922.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1929T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297168 | ||||||
chrX:297171
|
G | A | 3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-1926G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297171 | ||||||
chrX:297175
|
A | C | 3 | a0002c0005t0022g0035a0002c0005t0106g0077a0002c0019t0022g0138 | 3 | HG00639.hp1 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-1922A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297175 | ||||||
chrX:297176
|
T | C | 10 | a0001c0001t0057g0055a0001c0001t0074g0143a0001c0002t0090g0151others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-1921T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297176 | ||||||
chrX:297176
|
TCACATGG others(238): Show |
T | 14 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-1873_734-1629d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297176 | |||||
chrX:297178
|
A | ACATGGGG others(91): Show |
1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-1839_734-1838i others(100): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297178 | |||||
chrX:297178
|
A | T | 7 | a0001c0001t0057g0055a0001c0001t0074g0143a0001c0002t0090g0151others(4): Show | 7 | HG01168.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1919A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297178 | ||||||
chrX:297181
|
TG | T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1912delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297181 | |||||
chrX:297183
|
G | A | 1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-1914G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297183 | ||||||
chrX:297210
|
A | ACATTATT others(184): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1878_734-1877i others(193): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297210 | |||||
chrX:297210
|
A | C | 6 | a0001c0001t0012g0015a0001c0001t0027g0059a0001c0001t0052g0068others(3): Show | 6 | HG02257.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1887A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297210 | ||||||
chrX:297212
|
ATTATTCT others(532): Show |
A | 5 | a0001c0001t0001g0004a0001c0001t0024g0101a0001c0001t0070g0004others(2): Show | 5 | HG00558.hp2 NA18993.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-1838_734-1300d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297212 | |||||
chrX:297217
|
T | C | 1 | a0001c0002t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.734-1880T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297217 | ||||||
chrX:297223
|
T | C | 19 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(16): Show | 20 | HG01123.hp1 HG01346.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.734-1874T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297223 | ||||||
chrX:297224
|
A | C | 20 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(17): Show | 21 | HG01123.hp1 HG01346.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.734-1873A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297224 | ||||||
chrX:297225
|
T | C | 25 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(22): Show | 26 | HG01123.hp1 HG01168.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.734-1872T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297225 | ||||||
chrX:297225
|
T | TCACATGG others(42): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1839_734-1838i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297225 | |||||
chrX:297225
|
TCACATGG others(287): Show |
T | 1 | a0001c0001t0005g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.734-1811_734-1518d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297225 | |||||
chrX:297227
|
A | T | 5 | a0001c0001t0057g0055a0001c0001t0074g0143a0001c0002t0090g0151others(2): Show | 5 | HG01168.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-1870A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297227 | ||||||
chrX:297234
|
G | A | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-1863G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297234 | ||||||
chrX:297237
|
T | C | 1 | a0001c0002t0097g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.734-1860T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297237 | ||||||
chrX:297259
|
A | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(67): Show | 73 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.734-1838A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297259 | ||||||
chrX:297261
|
ATTATTCT others(483): Show |
A | 5 | a0001c0001t0009g0067a0001c0001t0029g0019a0001c0001t0030g0062others(2): Show | 5 | HG01496.hp1 HG02056.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-1811_734-1322d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297261 | |||||
chrX:297266
|
TCTGTCTA others(42): Show |
T | 7 | a0001c0001t0002g0050a0001c0001t0011g0125a0001c0001t0017g0007others(4): Show | 7 | HG01123.hp1 HG02896.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1811_734-1763d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297266 | |||||
chrX:297269
|
G | GTCTCCCA others(87): Show |
2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1825_734-1824i others(96): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297269 | |||||
chrX:297273
|
A | ACC | 2 | a0002c0005t0022g0035a0002c0005t0106g0077 | 2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-1824_734-1823i others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297273 | ||||||
chrX:297273
|
A | C | 1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-1824A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297273 | ||||||
chrX:297274
|
T | C | 5 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0003t0089g0011others(2): Show | 5 | HG00639.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-1823T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297274 | ||||||
chrX:297274
|
T | TCACATGG others(140): Show |
1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-1812_734-1811i others(149): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297274 | |||||
chrX:297274
|
TCACATGG others(238): Show |
T | 12 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(9): Show | 12 | HG01346.hp2 HG02559.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.734-1811_734-1567d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297274 | |||||
chrX:297274
|
TCACATGG others(336): Show |
T | 4 | a0001c0001t0001g0054a0001c0001t0066g0161a0001c0001t0113g0166others(1): Show | 4 | HG00408.hp2 HG02723.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1811_734-1469d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297274 | |||||
chrX:297274
|
TCACATGG others(434): Show |
T | 2 | a0001c0001t0009g0075a0001c0001t0037g0063 | 2 | NA18964.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.734-1811_734-1371d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297274 | |||||
chrX:297276
|
A | ACATGGGG others(90): Show |
1 | a0001c0001t0015g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.734-1812_734-1811i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297276 | |||||
chrX:297276
|
A | ATGGGGAT others(187): Show |
2 | a0002c0005t0022g0035a0002c0005t0106g0077 | 2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.734-1821_734-1820i others(196): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297276 | ||||||
chrX:297276
|
A | T | 4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0019t0022g0138others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-1821A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297276 | ||||||
chrX:297279
|
TG | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-1814delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297279 | |||||
chrX:297279
|
TGGGGATC others(141): Show |
T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1814_734-1667d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297279 | |||||
chrX:297281
|
G | A | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1816G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297281 | ||||||
chrX:297283
|
G | A | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1814G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297283 | ||||||
chrX:297285
|
TC | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-1811delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297285 | ||||||
chrX:297286
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(63): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.734-1811C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297286 | ||||||
chrX:297288
|
G | C | 10 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(7): Show | 10 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-1809G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297288 | ||||||
chrX:297291
|
C | T | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0055g0010 | 3 | HG02257.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1806C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297291 | ||||||
chrX:297308
|
A | C | 4 | a0001c0001t0012g0015a0001c0003t0058g0103a0001c0003t0065g0012others(1): Show | 4 | HG01123.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1789A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297308 | ||||||
chrX:297310
|
ATTATCCT others(287): Show |
A | 1 | a0001c0001t0011g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.734-1782_734-1489d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297310 | |||||
chrX:297310
|
ATTATCCT others(434): Show |
A | 31 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(28): Show | 32 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.734-1782_734-1342d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297310 | |||||
chrX:297314
|
TC | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-1781delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297314 | |||||
chrX:297315
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0012g0015others(26): Show | 30 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-1782C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297315 | ||||||
chrX:297321
|
T | C | 1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1776T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297321 | ||||||
chrX:297322
|
A | C | 1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1775A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297322 | ||||||
chrX:297323
|
T | C | 3 | a0001c0001t0012g0149a0001c0001t0015g0074a0001c0003t0107g0104 | 3 | HG02280.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.734-1774T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297323 | ||||||
chrX:297323
|
TCACATGG others(42): Show |
T | 4 | a0001c0001t0045g0031a0001c0001t0092g0089a0001c0002t0002g0134others(1): Show | 4 | HG00733.hp1 HG02155.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1691_734-1643d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297323 | |||||
chrX:297324
|
C | CA | 1 | a0001c0002t0105g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-1772dupA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297324 | |||||
chrX:297325
|
A | T | 2 | a0001c0001t0015g0074a0001c0003t0107g0104 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.734-1772A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297325 | ||||||
chrX:297332
|
G | A | 1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-1765G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297332 | ||||||
chrX:297357
|
C | A | 19 | a0000c0018t0101g0132a0001c0001t0011g0125a0001c0001t0012g0015others(16): Show | 19 | HG00735.hp1 HG01123.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-1740C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297357 | ||||||
chrX:297357
|
C | CCATTATT others(189): Show |
1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-1727_734-1726i others(198): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297357 | |||||
chrX:297357
|
CCATTATT others(189): Show |
C | 2 | a0001c0001t0074g0143a0001c0003t0060g0051 | 2 | HG01168.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.734-1726_734-1531d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297357 | |||||
chrX:297359
|
ATTATTCT others(385): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.734-1726_734-1335d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297359 | |||||
chrX:297362
|
A | G | 1 | a0001c0003t0065g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.734-1735A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297362 | ||||||
chrX:297364
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0073g0102a0001c0003t0089g0011 | 4 | HG01070.hp1 HG01071.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1733T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297364 | ||||||
chrX:297370
|
T | C | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1727T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297370 | ||||||
chrX:297371
|
C | A | 22 | a0001c0001t0001g0003a0001c0001t0012g0149a0001c0001t0015g0074others(19): Show | 23 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.734-1726C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297371 | ||||||
chrX:297372
|
C | CCACATGG others(528): Show |
1 | a0001c0002t0091g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.734-1692_734-1691i others(537): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297372 | |||||
chrX:297372
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0012g0149a0001c0001t0015g0074others(18): Show | 22 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-1725C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297372 | ||||||
chrX:297374
|
A | T | 1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-1723A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297374 | ||||||
chrX:297377
|
TG | T | 7 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(4): Show | 7 | HG01123.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-1716delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297377 | |||||
chrX:297406
|
C | A | 25 | a0001c0001t0012g0149a0001c0001t0018g0099a0001c0001t0018g0100others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.734-1691C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297406 | ||||||
chrX:297406
|
CCATTATT others(238): Show |
C | 1 | a0001c0001t0001g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.734-1677_734-1433d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297406 | |||||
chrX:297411
|
A | G | 3 | a0001c0001t0027g0059a0001c0003t0055g0010a0001c0003t0065g0012 | 3 | HG01123.hp2 HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1686A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297411 | ||||||
chrX:297413
|
T | C | 8 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(5): Show | 8 | HG01123.hp1 HG02896.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-1684T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297413 | ||||||
chrX:297420
|
C | A | 17 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0015g0074others(14): Show | 17 | HG01123.hp1 HG01123.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.734-1677C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297420 | ||||||
chrX:297421
|
C | CCACATGG others(42): Show |
9 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-1629_734-1628i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297421 | |||||
chrX:297421
|
C | T | 10 | a0001c0001t0015g0074a0001c0001t0027g0059a0001c0001t0052g0068others(7): Show | 10 | HG01123.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-1676C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297421 | ||||||
chrX:297423
|
A | ACATGGGA others(90): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1668_734-1667i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297423 | |||||
chrX:297423
|
A | T | 7 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(4): Show | 7 | HG01123.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-1674A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297423 | ||||||
chrX:297455
|
A | C | 2 | a0001c0002t0090g0151a0001c0003t0051g0071 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.734-1642A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297455 | ||||||
chrX:297457
|
A | ATTATTCT others(42): Show |
1 | a0001c0002t0110g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.734-1593_734-1545d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297457 | |||||
chrX:297457
|
ATTATTCT others(42): Show |
A | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-1593_734-1545d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297457 | |||||
chrX:297460
|
A | G | 2 | a0001c0001t0027g0059a0001c0003t0065g0012 | 2 | HG01123.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1637A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297460 | ||||||
chrX:297462
|
T | C | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1635T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297462 | ||||||
chrX:297469
|
C | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(35): Show | 38 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.734-1628C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297469 | ||||||
chrX:297470
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.734-1627C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297470 | ||||||
chrX:297472
|
A | T | 7 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(4): Show | 7 | HG01123.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-1625A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297472 | ||||||
chrX:297475
|
TG | T | 2 | a0000c0018t0101g0132a0001c0001t0086g0061 | 2 | HG01891.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.734-1618delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297475 | |||||
chrX:297482
|
T | C | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1615T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297482 | ||||||
chrX:297484
|
G | C | 1 | a0001c0003t0065g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.734-1613G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297484 | ||||||
chrX:297501
|
G | A | 9 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-1596G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297501 | ||||||
chrX:297504
|
C | A | 19 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0015g0074others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-1593C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297504 | ||||||
chrX:297505
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.734-1592T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297505 | ||||||
chrX:297506
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.734-1591G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297506 | ||||||
chrX:297506
|
GTTATTCT others(483): Show |
G | 1 | a0001c0003t0002g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.734-1495_734-1006d others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297506 | |||||
chrX:297511
|
T | C | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1586T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297511 | ||||||
chrX:297514
|
G | A | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1583G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297514 | ||||||
chrX:297517
|
TC | T | 1 | a0001c0002t0004g0109 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.734-1577delC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297517 | |||||
chrX:297518
|
C | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.734-1579C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297518 | ||||||
chrX:297519
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(35): Show | 38 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.734-1578C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297519 | ||||||
chrX:297521
|
A | T | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1576A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297521 | ||||||
chrX:297533
|
G | C | 2 | a0001c0001t0027g0059a0001c0003t0055g0010 | 2 | HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1564G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297533 | ||||||
chrX:297553
|
A | C | 10 | a0001c0001t0005g0084a0001c0001t0011g0125a0001c0001t0017g0007others(7): Show | 10 | HG01123.hp1 HG01123.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-1544A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297553 | ||||||
chrX:297567
|
A | C | 13 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(10): Show | 13 | HG01346.hp2 HG02559.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-1530A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297567 | ||||||
chrX:297568
|
T | C | 13 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(10): Show | 13 | HG01346.hp2 HG02559.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-1529T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297568 | ||||||
chrX:297568
|
T | TCACATGG others(136): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1496_734-1495i others(145): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297568 | |||||
chrX:297568
|
TCACATGG others(42): Show |
T | 6 | a0001c0001t0005g0084a0001c0001t0011g0125a0001c0001t0017g0007others(3): Show | 6 | HG01123.hp1 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1495_734-1447d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297568 | |||||
chrX:297570
|
A | ACATTGGG others(42): Show |
1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.734-1524_734-1523i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297570 | |||||
chrX:297573
|
TG | T | 12 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(9): Show | 12 | HG01346.hp2 HG02559.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.734-1520delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297573 | |||||
chrX:297577
|
G | GATTAGGA others(336): Show |
1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-1495_734-1494i others(345): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297577 | |||||
chrX:297599
|
G | A | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-1498G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297599 | ||||||
chrX:297601
|
G | GACATTAT others(1): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1496_734-1495i others(10): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297601 | ||||||
chrX:297602
|
C | A | 21 | a0001c0001t0012g0015a0001c0001t0018g0099a0001c0001t0018g0100others(18): Show | 21 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.734-1495C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297602 | ||||||
chrX:297602
|
C | CCATTATT others(42): Show |
2 | a0001c0001t0027g0059a0001c0003t0055g0010 | 2 | HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1495_734-1494i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297602 | ||||||
chrX:297602
|
C | CCATTATT others(336): Show |
1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-1495_734-1494i others(345): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297602 | ||||||
chrX:297603
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-1494T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297603 | ||||||
chrX:297604
|
G | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-1493G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297604 | ||||||
chrX:297604
|
G | GTCTCCCA others(34): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1492_734-1491i others(43): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297604 | |||||
chrX:297609
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-1488T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297609 | ||||||
chrX:297615
|
T | C | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1482T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297615 | ||||||
chrX:297616
|
C | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.734-1481C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297616 | ||||||
chrX:297617
|
C | CCACATGG others(287): Show |
1 | a0001c0003t0082g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.734-1348_734-1055d others(296): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297617 | |||||
chrX:297617
|
C | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.734-1480C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297617 | ||||||
chrX:297619
|
A | ACATGGGA others(41): Show |
2 | a0001c0003t0054g0094a0001c0003t0056g0092 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.734-1472_734-1471i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297619 | |||||
chrX:297619
|
A | ACATGGGA others(90): Show |
5 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-1472_734-1471i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297619 | |||||
chrX:297619
|
A | ACATGGGA others(770): Show |
1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1472_734-1471i others(779): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297619 | |||||
chrX:297619
|
A | T | 19 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(16): Show | 19 | HG00735.hp1 HG01346.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.734-1478A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297619 | ||||||
chrX:297622
|
TG | T | 1 | a0001c0001t0011g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.734-1471delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297622 | |||||
chrX:297629
|
T | TAGGACGT others(1267): Show |
1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-1398_734-1397i others(1276): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297629 | |||||
chrX:297634
|
C | T | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1463C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297634 | ||||||
chrX:297635
|
G | A | 1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-1462G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297635 | ||||||
chrX:297649
|
G | A | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1448G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297649 | ||||||
chrX:297651
|
A | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.734-1446A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297651 | ||||||
chrX:297658
|
T | C | 7 | a0001c0001t0005g0084a0001c0001t0011g0126a0001c0001t0018g0099others(4): Show | 7 | HG00099.hp2 HG01168.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1439T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297658 | ||||||
chrX:297665
|
A | C | 2 | a0001c0001t0012g0015a0001c0003t0088g0152 | 2 | HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.734-1432A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297665 | ||||||
chrX:297666
|
T | C | 15 | a0001c0001t0011g0126a0001c0001t0012g0015a0001c0001t0015g0073others(12): Show | 15 | HG01346.hp2 HG02559.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.734-1431T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297666 | ||||||
chrX:297668
|
A | T | 13 | a0001c0001t0011g0126a0001c0001t0015g0073a0001c0001t0016g0082others(10): Show | 13 | HG01346.hp2 HG02559.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1429A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297668 | ||||||
chrX:297678
|
T | C | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1419T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297678 | ||||||
chrX:297683
|
C | T | 5 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0003t0051g0071others(2): Show | 5 | HG00735.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-1414C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297683 | ||||||
chrX:297700
|
A | C | 25 | a0001c0001t0001g0054a0001c0001t0005g0084a0001c0001t0015g0073others(22): Show | 25 | HG00408.hp2 HG00735.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.734-1397A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297700 | ||||||
chrX:297702
|
ATTATTCT others(42): Show |
A | 15 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-1383_734-1335d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297702 | |||||
chrX:297707
|
T | C | 7 | a0001c0001t0001g0054a0001c0001t0005g0084a0001c0001t0066g0161others(4): Show | 7 | HG00408.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-1390T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297707 | ||||||
chrX:297714
|
C | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0005g0084others(27): Show | 31 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.734-1383C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297714 | ||||||
chrX:297715
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0005g0084others(25): Show | 29 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.734-1382C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297715 | ||||||
chrX:297717
|
A | ACATGGGA others(41): Show |
1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-1374_734-1373i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297717 | |||||
chrX:297717
|
A | T | 2 | a0001c0001t0011g0126a0001c0003t0107g0104 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.734-1380A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297717 | ||||||
chrX:297718
|
C | T | 1 | a0001c0001t0074g0143 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.734-1379C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297718 | ||||||
chrX:297720
|
TG | T | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1373delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297720 | |||||
chrX:297733
|
G | A | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1364G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297733 | ||||||
chrX:297746
|
G | A | 3 | a0001c0001t0027g0059a0001c0003t0055g0010a0001c0003t0065g0012 | 3 | HG01123.hp2 HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1351G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297746 | ||||||
chrX:297747
|
G | A | 1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-1350G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297747 | ||||||
chrX:297749
|
C | A | 27 | a0001c0001t0001g0003a0001c0001t0005g0084a0001c0001t0011g0125others(24): Show | 28 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.734-1348C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297749 | ||||||
chrX:297749
|
C | CCATTATT others(42): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1348_734-1347i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297749 | ||||||
chrX:297750
|
T | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0005g0084others(51): Show | 56 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.734-1347T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297750 | ||||||
chrX:297751
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0005g0084others(51): Show | 56 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.734-1346G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297751 | ||||||
chrX:297751
|
G | GTTATTCT others(335): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1335_734-1334i others(344): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297751 | |||||
chrX:297756
|
T | C | 10 | a0001c0001t0001g0046a0001c0001t0011g0125a0001c0001t0015g0074others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-1341T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297756 | ||||||
chrX:297762
|
T | C | 8 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-1335T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297762 | ||||||
chrX:297763
|
A | C | 12 | a0001c0001t0027g0059a0001c0001t0073g0102a0001c0003t0006g0041others(9): Show | 12 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.734-1334A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297763 | ||||||
chrX:297764
|
T | C | 14 | a0001c0001t0027g0059a0001c0001t0052g0068a0001c0001t0073g0102others(11): Show | 14 | HG01123.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.734-1333T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297764 | ||||||
chrX:297766
|
A | ACATGGGA others(42): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1325_734-1324i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297766 | |||||
chrX:297766
|
A | T | 2 | a0001c0001t0052g0068a0001c0001t0086g0061 | 2 | HG01891.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.734-1331A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297766 | ||||||
chrX:297767
|
C | T | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.734-1330C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297767 | ||||||
chrX:297773
|
G | A | 4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0005t0022g0035others(1): Show | 4 | HG00735.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-1324G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297773 | ||||||
chrX:297798
|
C | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0054others(53): Show | 57 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.734-1299C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297798 | ||||||
chrX:297798
|
C | CCATTATT others(189): Show |
4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0005t0022g0035others(1): Show | 4 | HG00735.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-1285_734-1284i others(198): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297798 | |||||
chrX:297798
|
CCATTATT others(42): Show |
C | 5 | a0001c0001t0011g0125a0001c0001t0017g0007a0001c0001t0043g0017others(2): Show | 5 | HG01123.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-1138_734-1090d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297798 | |||||
chrX:297805
|
T | C | 39 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(36): Show | 40 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.734-1292T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297805 | ||||||
chrX:297808
|
G | A | 1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-1289G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297808 | ||||||
chrX:297812
|
A | C | 5 | a0001c0001t0001g0003a0001c0001t0073g0102a0001c0003t0088g0152others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1285A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297812 | ||||||
chrX:297813
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0073g0102a0001c0001t0086g0061others(3): Show | 7 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1284T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297813 | ||||||
chrX:297813
|
T | TCACATGG others(42): Show |
1 | a0001c0002t0004g0133 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.734-1237_734-1236i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297813 | |||||
chrX:297815
|
A | ACATGGGG others(90): Show |
6 | a0001c0003t0006g0041a0001c0003t0006g0042a0001c0003t0006g0114others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-1237_734-1236i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297815 | |||||
chrX:297815
|
A | T | 1 | a0001c0001t0086g0061 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.734-1282A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297815 | ||||||
chrX:297819
|
G | T | 5 | a0001c0003t0023g0020a0001c0003t0023g0021a0001c0010t0042g0163others(2): Show | 5 | HG00735.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-1278G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297819 | ||||||
chrX:297845
|
G | A | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1252G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297845 | ||||||
chrX:297847
|
A | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(45): Show | 49 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.734-1250A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297847 | ||||||
chrX:297848
|
C | T | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-1249C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297848 | ||||||
chrX:297849
|
A | G | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-1248A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297849 | ||||||
chrX:297854
|
T | C | 14 | a0001c0001t0009g0067a0001c0001t0011g0125a0001c0001t0017g0007others(11): Show | 14 | HG00639.hp1 HG01123.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-1243T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297854 | ||||||
chrX:297854
|
T | TCTGTCTC others(41): Show |
3 | a0001c0001t0027g0059a0001c0003t0055g0010a0001c0003t0065g0012 | 3 | HG01123.hp2 HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1237_734-1236i others(50): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297854 | |||||
chrX:297854
|
T | TCTGTCTC others(90): Show |
1 | a0011c0016t0006g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-1237_734-1236i others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297854 | |||||
chrX:297857
|
G | GTCTCCCA others(379): Show |
1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.734-1237_734-1236i others(388): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297857 | |||||
chrX:297857
|
G | GTCTCCCA others(136): Show |
2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1237_734-1236i others(145): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297857 | |||||
chrX:297861
|
A | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(29): Show | 32 | HG00323.hp1 HG01168.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-1236A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297861 | ||||||
chrX:297862
|
T | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0005g0038others(40): Show | 43 | HG00323.hp1 HG01123.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.734-1235T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297862 | ||||||
chrX:297864
|
A | T | 11 | a0001c0001t0027g0059a0001c0003t0006g0041a0001c0003t0006g0042others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.734-1233A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297864 | ||||||
chrX:297879
|
C | T | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1218C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297879 | ||||||
chrX:297896
|
A | C | 27 | a0001c0001t0001g0004a0001c0001t0003g0025a0001c0001t0003g0027others(24): Show | 27 | HG00558.hp2 HG00735.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.734-1201A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297896 | ||||||
chrX:297902
|
TTCTG | T | 2 | a0001c0001t0073g0102a0001c0002t0076g0107 | 2 | NA19055.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.734-1191_734-1188d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297902 | |||||
chrX:297903
|
T | C | 21 | a0001c0001t0001g0004a0001c0001t0015g0073a0001c0001t0016g0082others(18): Show | 21 | HG00558.hp2 HG01346.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.734-1194T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297903 | ||||||
chrX:297906
|
G | GTCTCCCA others(38): Show |
1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-1188_734-1187i others(47): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297906 | |||||
chrX:297909
|
T | C | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-1188T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297909 | ||||||
chrX:297910
|
A | C | 14 | a0001c0001t0001g0054a0001c0001t0011g0125a0001c0001t0011g0126others(11): Show | 14 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-1187A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297910 | ||||||
chrX:297911
|
T | C | 25 | a0001c0001t0001g0054a0001c0001t0011g0125a0001c0001t0011g0126others(22): Show | 25 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-1186T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297911 | ||||||
chrX:297911
|
TCACATGG others(91): Show |
T | 2 | a0001c0001t0001g0004a0001c0001t0070g0004 | 2 | HG00558.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.734-1089_734-992de others(99): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297911 | |||||
chrX:297913
|
A | ACATGGGG others(385): Show |
3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-1140_734-1139i others(394): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297913 | |||||
chrX:297913
|
A | T | 11 | a0001c0001t0027g0059a0001c0003t0006g0041a0001c0003t0006g0042others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.734-1184A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297913 | ||||||
chrX:297916
|
TG | T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1177delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297916 | |||||
chrX:297928
|
C | T | 2 | a0001c0003t0053g0162a0001c0003t0089g0011 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.734-1169C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297928 | ||||||
chrX:297937
|
C | A | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1160C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297937 | ||||||
chrX:297945
|
A | C | 19 | a0001c0001t0012g0015a0001c0001t0015g0073a0001c0001t0016g0082others(16): Show | 19 | HG01123.hp2 HG01346.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-1152A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297945 | ||||||
chrX:297945
|
A | CCATTATT others(336): Show |
1 | a0001c0002t0004g0133 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.734-1153_734-1152i others(345): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297945 | ||||||
chrX:297952
|
T | C | 15 | a0001c0001t0011g0126a0001c0001t0012g0015a0001c0001t0015g0073others(12): Show | 15 | HG01346.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.734-1145T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297952 | ||||||
chrX:297952
|
T | TCTGTCCC others(2047): Show |
1 | a0002c0005t0022g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.734-1140_734-1139i others(2056): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297952 | |||||
chrX:297959
|
A | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0054others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-1138A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297959 | ||||||
chrX:297960
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0054others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-1137T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297960 | ||||||
chrX:297960
|
T | TCACATGG others(185): Show |
1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-1104_734-1103i others(194): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297960 | |||||
chrX:297960
|
TCACATGG others(42): Show |
T | 2 | a0001c0001t0011g0126a0001c0001t0113g0166 | 2 | HG02647.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.734-1089_734-1041d others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297960 | |||||
chrX:297962
|
A | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1135A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297962 | ||||||
chrX:297989
|
TG | T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1104delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 297989 | |||||
chrX:297994
|
A | C | 2 | a0001c0001t0001g0054a0001c0003t0051g0071 | 2 | HG02615.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.734-1103A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297994 | ||||||
chrX:297995
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.734-1102C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297995 | ||||||
chrX:297996
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.734-1101A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297996 | ||||||
chrX:298001
|
T | C | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-1096T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298001 | ||||||
chrX:298008
|
C | A | 15 | a0001c0001t0009g0067a0001c0001t0015g0074a0001c0001t0029g0019others(12): Show | 15 | HG00408.hp2 HG00735.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-1089C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298008 | ||||||
chrX:298009
|
C | T | 15 | a0001c0001t0009g0067a0001c0001t0015g0074a0001c0001t0029g0019others(12): Show | 15 | HG00099.hp2 HG00408.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-1088C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298009 | ||||||
chrX:298009
|
CCACATGG others(42): Show |
C | 2 | a0001c0001t0080g0088a0001c0001t0086g0061 | 2 | HG01891.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.734-942_734-894del others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298009 | |||||
chrX:298009
|
CCACATGG others(140): Show |
C | 6 | a0001c0001t0001g0158a0001c0001t0068g0034a0001c0001t0079g0001others(3): Show | 6 | HG00323.hp1 HG01168.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1040_734-894de others(1): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298009 | |||||
chrX:298011
|
A | T | 1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-1086A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298011 | ||||||
chrX:298014
|
TG | T | 7 | a0001c0001t0052g0068a0001c0003t0006g0041a0001c0003t0006g0042others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1079delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298014 | |||||
chrX:298017
|
G | GGATTAGG others(773): Show |
1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-1031_734-1030i others(782): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298017 | |||||
chrX:298021
|
T | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-1076T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298021 | ||||||
chrX:298038
|
TG | T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1055delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298038 | |||||
chrX:298040
|
G | A | 1 | a0011c0016t0006g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-1057G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298040 | ||||||
chrX:298043
|
A | ACATTATT others(42): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-1040_734-1039i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298043 | |||||
chrX:298043
|
A | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0046others(14): Show | 18 | HG00558.hp2 HG00735.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.734-1054A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298043 | ||||||
chrX:298044
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0046a0011c0016t0006g0076 | 4 | HG01070.hp1 HG01071.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1053C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298044 | ||||||
chrX:298045
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0046a0011c0016t0006g0076 | 4 | HG01070.hp1 HG01071.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1052A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298045 | ||||||
chrX:298049
|
TTCTG | T | 2 | a0001c0001t0001g0054a0001c0001t0009g0065 | 2 | HG02148.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.734-1044_734-1041d others(6): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298049 | |||||
chrX:298050
|
T | C | 8 | a0001c0001t0011g0126a0001c0001t0052g0068a0001c0003t0006g0041others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-1047T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298050 | ||||||
chrX:298050
|
T | TCTATCAC others(38): Show |
1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-1045_734-1044i others(47): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298050 | |||||
chrX:298053
|
G | GTCTACCT others(87): Show |
7 | a0001c0001t0052g0068a0001c0003t0006g0041a0001c0003t0006g0042others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-1040_734-1039i others(96): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298053 | |||||
chrX:298056
|
T | C | 3 | a0001c0001t0027g0059a0001c0003t0055g0010a0001c0003t0065g0012 | 3 | HG01123.hp2 HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-1041T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298056 | ||||||
chrX:298056
|
TA | T | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1040delA | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298056 | ||||||
chrX:298057
|
A | ACC | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1040_734-1039i others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298057 | ||||||
chrX:298057
|
A | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(20): Show | 24 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.734-1040A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298057 | ||||||
chrX:298058
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(22): Show | 26 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.734-1039T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298058 | ||||||
chrX:298060
|
A | ACATGGGA others(42): Show |
1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-1031_734-1030i others(51): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298060 | |||||
chrX:298060
|
A | ATGGGGAT others(89): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1037_734-1036i others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298060 | ||||||
chrX:298060
|
A | T | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1037A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298060 | ||||||
chrX:298090
|
G | GCT | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1007_734-1006i others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298090 | ||||||
chrX:298091
|
GACATTAT others(1): Show |
G | 2 | a0001c0001t0005g0038a0001c0002t0019g0130 | 2 | HG02080.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.734-1005_734-998de others(9): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298091 | ||||||
chrX:298091
|
GACATTAT others(45): Show |
G | 1 | a0001c0001t0057g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-1005_734-954de others(53): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298091 | ||||||
chrX:298092
|
A | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(19): Show | 23 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.734-1005A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298092 | ||||||
chrX:298092
|
ACATTATT others(238): Show |
A | 1 | a0001c0001t0001g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.734-893_734-649del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298092 | |||||
chrX:298093
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0005g0084a0001c0001t0007g0121others(6): Show | 9 | HG00438.hp1 HG01361.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-1004C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298093 | ||||||
chrX:298094
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0005g0084a0001c0001t0007g0121others(6): Show | 9 | HG00438.hp1 HG01361.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-1003A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298094 | ||||||
chrX:298098
|
TTCTG | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0046 | 3 | HG01070.hp1 HG01071.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.734-995_734-992del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298098 | |||||
chrX:298099
|
T | C | 3 | a0001c0001t0086g0061a0001c0003t0053g0162a0001c0003t0088g0152 | 3 | HG01891.hp2 HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.734-998T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298099 | ||||||
chrX:298102
|
GTCTATCA others(34): Show |
G | 2 | a0001c0001t0005g0038a0001c0002t0019g0130 | 2 | HG02080.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.734-993_734-953del others(41): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298102 | |||||
chrX:298106
|
A | C | 33 | a0001c0001t0001g0005a0001c0001t0005g0084a0001c0001t0007g0121others(30): Show | 34 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.734-991A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298106 | ||||||
chrX:298107
|
T | C | 40 | a0001c0001t0001g0005a0001c0001t0005g0084a0001c0001t0007g0121others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.734-990T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298107 | ||||||
chrX:298107
|
TCACATGG others(91): Show |
T | 2 | a0001c0001t0043g0017a0001c0002t0093g0137 | 2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.734-858_734-761del others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298107 | |||||
chrX:298109
|
A | ACATGGGG others(90): Show |
1 | a0001c0003t0055g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734-943_734-942ins others(97): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298109 | |||||
chrX:298109
|
A | T | 8 | a0001c0001t0052g0068a0001c0003t0006g0041a0001c0003t0006g0042others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-988A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298109 | ||||||
chrX:298119
|
T | C | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-978T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298119 | ||||||
chrX:298124
|
C | T | 8 | a0001c0001t0073g0102a0001c0003t0006g0041a0001c0003t0006g0042others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-973C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298124 | ||||||
chrX:298140
|
GACATTAT others(1): Show |
G | 1 | a0001c0001t0066g0161 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.734-956_734-949del others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298140 | ||||||
chrX:298141
|
A | ACATTATT others(139): Show |
1 | a0011c0016t0006g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-943_734-942ins others(146): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298141 | |||||
chrX:298141
|
A | C | 16 | a0001c0001t0001g0005a0001c0001t0005g0084a0001c0001t0007g0121others(13): Show | 16 | HG00099.hp2 HG00438.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-956A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298141 | ||||||
chrX:298142
|
C | T | 1 | a0001c0003t0014g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.734-955C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298142 | ||||||
chrX:298143
|
A | G | 1 | a0001c0003t0014g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.734-954A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298143 | ||||||
chrX:298147
|
TTCTG | T | 1 | a0001c0001t0005g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.734-946_734-943del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298147 | |||||
chrX:298148
|
T | C | 3 | a0001c0001t0086g0061a0001c0003t0088g0152a0001c0010t0042g0163 | 3 | HG01891.hp2 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.734-949T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298148 | ||||||
chrX:298148
|
T | TCTGTCTA others(42): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-908_734-907ins others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298148 | |||||
chrX:298148
|
T | TCTGTCTA others(91): Show |
1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.734-936_734-935ins others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298148 | |||||
chrX:298151
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0007g0121a0001c0001t0028g0070others(5): Show | 8 | HG00438.hp1 HG01361.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-946G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298151 | ||||||
chrX:298151
|
G | GTCTCCCA others(135): Show |
2 | a0001c0001t0027g0059a0001c0003t0065g0012 | 2 | HG01123.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-943_734-942ins others(142): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298151 | |||||
chrX:298151
|
GTCTATCA others(34): Show |
G | 1 | a0001c0001t0066g0161 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.734-944_734-904del others(41): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298151 | |||||
chrX:298152
|
TCTATCAC others(46): Show |
T | 1 | a0001c0001t0074g0143 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.734-943_734-891del others(53): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298152 | |||||
chrX:298152
|
TCTATCAC others(144): Show |
T | 7 | a0001c0001t0001g0005a0001c0001t0007g0121a0001c0001t0028g0070others(4): Show | 7 | HG00438.hp1 HG01361.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-943_734-793del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298152 | |||||
chrX:298155
|
A | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.734-942A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298155 | ||||||
chrX:298156
|
T | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.734-941T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298156 | ||||||
chrX:298156
|
TCACATGG others(42): Show |
T | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-893_734-845del others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298156 | |||||
chrX:298158
|
A | ACATGGGG others(91): Show |
1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-894_734-893ins others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298158 | |||||
chrX:298158
|
A | T | 2 | a0001c0003t0055g0010a0001c0010t0042g0163 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.734-939A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298158 | ||||||
chrX:298173
|
C | T | 4 | a0001c0003t0023g0020a0001c0003t0023g0021a0002c0019t0022g0138others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-924C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298173 | ||||||
chrX:298190
|
A | C | 9 | a0001c0001t0005g0038a0001c0001t0015g0074a0001c0001t0017g0007others(6): Show | 9 | HG00099.hp2 HG02080.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-907A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298190 | ||||||
chrX:298190
|
ACATTATT others(140): Show |
A | 1 | a0001c0001t0005g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.734-893_734-747del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298190 | |||||
chrX:298191
|
C | T | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.734-906C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298191 | ||||||
chrX:298192
|
A | G | 1 | a0001c0001t0113g0166 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.734-905A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298192 | ||||||
chrX:298195
|
A | G | 15 | a0001c0001t0004g0028a0001c0001t0004g0045a0001c0001t0026g0064others(12): Show | 15 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.734-902A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298195 | ||||||
chrX:298197
|
T | C | 5 | a0001c0001t0011g0125a0001c0001t0017g0007a0001c0003t0055g0010others(2): Show | 5 | HG02257.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-900T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298197 | ||||||
chrX:298200
|
G | A | 5 | a0001c0001t0005g0038a0001c0001t0057g0055a0001c0002t0019g0130others(2): Show | 5 | HG00099.hp2 HG02080.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-897G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298200 | ||||||
chrX:298201
|
TCTCC | T | 4 | a0001c0001t0005g0038a0001c0001t0057g0055a0001c0002t0019g0130others(1): Show | 4 | HG02080.hp1 HG02615.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-894_734-891del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298201 | |||||
chrX:298201
|
TCTCCCAC others(95): Show |
T | 1 | a0001c0003t0014g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.734-894_734-793del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298201 | |||||
chrX:298203
|
T | C | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-894T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298203 | ||||||
chrX:298204
|
C | A | 16 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(13): Show | 16 | HG01123.hp2 HG01361.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-893C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298204 | ||||||
chrX:298205
|
C | T | 13 | a0001c0001t0011g0125a0001c0001t0012g0015a0001c0001t0017g0007others(10): Show | 13 | HG01361.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-892C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298205 | ||||||
chrX:298207
|
A | T | 3 | a0001c0001t0027g0059a0001c0003t0055g0010a0001c0003t0065g0012 | 3 | HG01123.hp2 HG02257.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-890A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298207 | ||||||
chrX:298210
|
TG | T | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-883delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298210 | |||||
chrX:298217
|
T | C | 4 | a0001c0001t0073g0102a0001c0003t0023g0020a0001c0003t0023g0021others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-880T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298217 | ||||||
chrX:298222
|
C | T | 2 | a0001c0001t0027g0059a0001c0003t0065g0012 | 2 | HG01123.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-875C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298222 | ||||||
chrX:298223
|
G | A | 2 | a0001c0001t0018g0099a0001c0001t0018g0100 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-874G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298223 | ||||||
chrX:298226
|
G | T | 1 | a0001c0002t0046g0145 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.734-871G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298226 | ||||||
chrX:298238
|
GACATTAT others(1): Show |
G | 1 | a0001c0002t0076g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.734-858_734-851del others(8): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298238 | ||||||
chrX:298239
|
A | ACATTATC others(42): Show |
1 | a0001c0001t0015g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.734-852_734-851ins others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298239 | |||||
chrX:298239
|
A | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(52): Show | 56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.734-858A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298239 | ||||||
chrX:298240
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.734-857C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298240 | ||||||
chrX:298241
|
A | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.734-856A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298241 | ||||||
chrX:298245
|
TTCTG | T | 2 | a0001c0001t0066g0161a0001c0001t0113g0166 | 2 | HG00408.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.734-848_734-845del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298245 | |||||
chrX:298246
|
T | C | 6 | a0001c0001t0011g0125a0001c0001t0015g0074a0001c0001t0017g0007others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-851T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298246 | ||||||
chrX:298246
|
T | TCTGTCCC others(820): Show |
1 | a0011c0016t0006g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-846_734-845ins others(827): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298246 | |||||
chrX:298246
|
T | TCTGTCTA others(189): Show |
3 | a0001c0003t0006g0042a0001c0003t0006g0114a0001c0003t0054g0094 | 3 | HG01891.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.734-810_734-809ins others(196): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298246 | |||||
chrX:298246
|
T | TCTGTCTC others(481): Show |
1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-845_734-844ins others(488): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298246 | |||||
chrX:298249
|
GTCTATCA others(34): Show |
G | 1 | a0001c0002t0076g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.734-846_734-806del others(41): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298249 | |||||
chrX:298253
|
A | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(39): Show | 43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.734-844A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298253 | ||||||
chrX:298254
|
T | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(40): Show | 44 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.734-843T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298254 | ||||||
chrX:298256
|
A | T | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-841A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298256 | ||||||
chrX:298257
|
CAT | C | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-839_734-838del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298257 | ||||||
chrX:298259
|
TG | T | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-834delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298259 | |||||
chrX:298271
|
C | T | 2 | a0001c0002t0046g0145a0001c0002t0047g0144 | 2 | NA18944.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.734-826C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298271 | ||||||
chrX:298288
|
A | C | 49 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(46): Show | 50 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.734-809A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298288 | ||||||
chrX:298288
|
ACATTATT others(42): Show |
A | 2 | a0001c0001t0066g0161a0001c0001t0113g0166 | 2 | HG00408.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.734-795_734-747del others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298288 | |||||
chrX:298288
|
ACATTATT others(287): Show |
A | 1 | a0001c0001t0002g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.734-795_734-502del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298288 | |||||
chrX:298289
|
C | T | 4 | a0001c0001t0012g0015a0001c0001t0080g0088a0001c0001t0086g0061others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-808C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298289 | ||||||
chrX:298290
|
A | G | 4 | a0001c0001t0012g0015a0001c0001t0080g0088a0001c0001t0086g0061others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-807A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298290 | ||||||
chrX:298295
|
T | C | 17 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(14): Show | 17 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.734-802T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298295 | ||||||
chrX:298295
|
TCTGTCTC others(434): Show |
T | 2 | a0001c0001t0001g0004a0001c0001t0070g0004 | 2 | HG00558.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.734-795_734-355del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298295 | |||||
chrX:298298
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.734-799G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298298 | ||||||
chrX:298299
|
TCTCC | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0086others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.734-796_734-793del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298299 | |||||
chrX:298302
|
C | A | 24 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(21): Show | 24 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.734-795C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298302 | ||||||
chrX:298303
|
C | T | 23 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(20): Show | 23 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.734-794C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298303 | ||||||
chrX:298303
|
CCACATGG others(91): Show |
C | 8 | a0001c0001t0005g0038a0001c0001t0011g0125a0001c0001t0017g0007others(5): Show | 8 | HG02080.hp1 HG02976.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-760_734-663del others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298303 | |||||
chrX:298305
|
A | T | 1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-792A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298305 | ||||||
chrX:298308
|
TG | T | 1 | a0001c0003t0055g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734-785delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298308 | |||||
chrX:298320
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0009g0067others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-777C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298320 | ||||||
chrX:298337
|
C | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0046others(66): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.734-760C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298337 | ||||||
chrX:298337
|
C | CCATTATT others(238): Show |
1 | a0001c0003t0065g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.734-712_734-711ins others(245): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298337 | |||||
chrX:298337
|
C | CCATTATT others(189): Show |
2 | a0001c0003t0006g0041a0001c0003t0056g0092 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.734-740_734-739ins others(196): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298337 | |||||
chrX:298337
|
C | CCATTATT others(189): Show |
1 | a0001c0003t0104g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.734-740_734-739ins others(196): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298337 | |||||
chrX:298338
|
C | T | 6 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0023g0020others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-759C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298338 | ||||||
chrX:298339
|
A | G | 6 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0023g0020others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-758A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298339 | ||||||
chrX:298343
|
TTCTG | T | 3 | a0001c0001t0012g0015a0001c0001t0080g0088a0001c0002t0076g0107 | 3 | HG02976.hp1 NA19055.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.734-750_734-747del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298343 | |||||
chrX:298344
|
T | C | 16 | a0001c0001t0015g0073a0001c0001t0016g0082a0001c0001t0016g0098others(13): Show | 16 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-753T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298344 | ||||||
chrX:298344
|
T | TCTGTCTA others(238): Show |
1 | a0001c0001t0027g0059 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.734-712_734-711ins others(245): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298344 | |||||
chrX:298347
|
G | GTCTACCT others(87): Show |
1 | a0001c0003t0055g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734-746_734-745ins others(94): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298347 | |||||
chrX:298347
|
G | GTCTATCA others(4873): Show |
1 | a0002c0005t0106g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-712_734-711ins others(4880): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298347 | |||||
chrX:298351
|
A | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-746A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298351 | ||||||
chrX:298352
|
T | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-745T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298352 | ||||||
chrX:298364
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0009g0067others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-733T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298364 | ||||||
chrX:298369
|
C | T | 1 | a0001c0001t0073g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.734-728C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298369 | ||||||
chrX:298386
|
A | ACATTATT others(777): Show |
1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-663_734-662ins others(784): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298386 | |||||
chrX:298386
|
A | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0009g0067others(9): Show | 13 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-711A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298386 | ||||||
chrX:298387
|
C | T | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-710C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298387 | ||||||
chrX:298388
|
A | G | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-709A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298388 | ||||||
chrX:298393
|
T | C | 4 | a0001c0001t0011g0126a0001c0001t0027g0059a0001c0003t0065g0012others(1): Show | 4 | HG01123.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-704T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298393 | ||||||
chrX:298400
|
A | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(67): Show | 72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.734-697A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298400 | ||||||
chrX:298401
|
T | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.734-696T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298401 | ||||||
chrX:298403
|
A | ACATGGGG others(1790): Show |
1 | a0002c0005t0022g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.734-680_734-679ins others(1797): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298403 | |||||
chrX:298403
|
A | T | 3 | a0001c0003t0055g0010a0001c0003t0107g0104a0002c0005t0106g0077 | 3 | HG02257.hp1 HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.734-694A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298403 | ||||||
chrX:298404
|
CAT | C | 6 | a0001c0001t0001g0046a0001c0001t0009g0067a0001c0001t0029g0019others(3): Show | 6 | HG01496.hp1 HG02056.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-692_734-691del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298404 | ||||||
chrX:298413
|
T | C | 1 | a0001c0001t0080g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.734-684T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298413 | ||||||
chrX:298414
|
A | C | 3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-683A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298414 | ||||||
chrX:298418
|
C | CGTGGACA others(331): Show |
1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-650_734-649ins others(338): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298418 | |||||
chrX:298418
|
C | CGTGGACA others(42): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-663_734-662ins others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298418 | |||||
chrX:298418
|
C | T | 1 | a0001c0003t0055g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734-679C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298418 | ||||||
chrX:298435
|
A | C | 19 | a0001c0001t0011g0126a0001c0001t0027g0059a0001c0001t0080g0088others(16): Show | 19 | HG00639.hp1 HG01123.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.734-662A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298435 | ||||||
chrX:298436
|
C | T | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-661C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298436 | ||||||
chrX:298437
|
A | G | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-660A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298437 | ||||||
chrX:298442
|
T | C | 16 | a0001c0001t0011g0126a0001c0001t0027g0059a0001c0003t0006g0041others(13): Show | 16 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.734-655T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298442 | ||||||
chrX:298445
|
G | GTCTCCCA others(87): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-649_734-648ins others(94): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298445 | |||||
chrX:298449
|
A | C | 10 | a0001c0001t0001g0046a0001c0001t0009g0067a0001c0001t0012g0015others(7): Show | 10 | HG01496.hp1 HG01891.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-648A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298449 | ||||||
chrX:298450
|
T | C | 10 | a0001c0001t0001g0046a0001c0001t0009g0067a0001c0001t0012g0015others(7): Show | 10 | HG01496.hp1 HG01891.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-647T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298450 | ||||||
chrX:298452
|
A | ACATGGGG others(140): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-631_734-630ins others(147): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298452 | |||||
chrX:298453
|
CAT | C | 1 | a0001c0001t0080g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.734-643_734-642del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298453 | ||||||
chrX:298455
|
TG | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-638delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298455 | |||||
chrX:298462
|
T | C | 1 | a0001c0002t0076g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.734-635T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298462 | ||||||
chrX:298467
|
C | T | 2 | a0001c0001t0001g0003a0002c0019t0022g0138 | 3 | HG00639.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.734-630C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298467 | ||||||
chrX:298484
|
A | C | 31 | a0001c0001t0004g0028a0001c0001t0011g0125a0001c0001t0011g0126others(28): Show | 32 | HG01123.hp1 HG01123.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-613A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298484 | ||||||
chrX:298485
|
C | T | 18 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(15): Show | 19 | HG01123.hp1 HG01346.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-612C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298485 | ||||||
chrX:298486
|
A | G | 18 | a0001c0001t0011g0125a0001c0001t0011g0126a0001c0001t0015g0073others(15): Show | 19 | HG01123.hp1 HG01346.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-611A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298486 | ||||||
chrX:298491
|
T | C | 10 | a0001c0001t0027g0059a0001c0003t0006g0041a0001c0003t0006g0042others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-606T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298491 | ||||||
chrX:298491
|
T | TCTGTCTA others(140): Show |
1 | a0001c0003t0053g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.734-600_734-599ins others(147): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298491 | |||||
chrX:298491
|
TCTGTCTC others(238): Show |
T | 2 | a0001c0001t0001g0046a0001c0001t0086g0061 | 2 | HG01891.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.734-599_734-355del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298491 | |||||
chrX:298498
|
C | A | 25 | a0001c0001t0004g0028a0001c0001t0009g0067a0001c0001t0012g0015others(22): Show | 25 | HG01123.hp2 HG01496.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-599C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298498 | ||||||
chrX:298499
|
C | CCACATGG others(923): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-565_734-564ins others(930): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298499 | |||||
chrX:298499
|
C | CCACATGG others(434): Show |
1 | a0001c0001t0052g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-565_734-564ins others(441): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298499 | |||||
chrX:298499
|
C | T | 24 | a0001c0001t0004g0028a0001c0001t0009g0067a0001c0001t0012g0015others(21): Show | 24 | HG01123.hp2 HG01496.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.734-598C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298499 | ||||||
chrX:298501
|
A | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-596A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298501 | ||||||
chrX:298502
|
CAT | C | 1 | a0001c0002t0076g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.734-594_734-593del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298502 | ||||||
chrX:298516
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(58): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.734-581C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298516 | ||||||
chrX:298533
|
A | C | 2 | a0001c0003t0053g0162a0001c0003t0055g0010 | 2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.734-564A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298533 | ||||||
chrX:298539
|
TTCTG | T | 1 | a0001c0002t0002g0135 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.734-554_734-551del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298539 | |||||
chrX:298540
|
T | TCTGTCTA others(42): Show |
1 | a0001c0001t0015g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.734-516_734-515ins others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298540 | |||||
chrX:298540
|
T | TCTGTCTA others(385): Show |
1 | a0001c0003t0055g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.734-509_734-508ins others(392): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298540 | |||||
chrX:298540
|
TCTGTCTA others(189): Show |
T | 1 | a0001c0001t0080g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.734-515_734-320del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298540 | |||||
chrX:298541
|
CT | C | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-555delT | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298541 | ||||||
chrX:298547
|
A | C | 7 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0018g0099others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-550A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298547 | ||||||
chrX:298548
|
T | C | 7 | a0001c0001t0012g0015a0001c0001t0012g0149a0001c0001t0018g0099others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-549T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298548 | ||||||
chrX:298550
|
A | ACATGGGG others(287): Show |
3 | a0001c0003t0023g0020a0001c0003t0023g0021a0008c0011t0108g0022 | 3 | HG02630.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.734-516_734-515ins others(294): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298550 | |||||
chrX:298560
|
T | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(52): Show | 57 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.734-537T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298560 | ||||||
chrX:298565
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0012g0015a0002c0005t0022g0035others(1): Show | 5 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-532C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298565 | ||||||
chrX:298572
|
A | G | 1 | a0001c0001t0067g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.734-525A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298572 | ||||||
chrX:298577
|
T | TG | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-516dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298577 | |||||
chrX:298581
|
G | A | 1 | a0001c0001t0095g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.734-516G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298581 | ||||||
chrX:298582
|
C | A | 39 | a0001c0001t0001g0003a0001c0001t0009g0067a0001c0001t0011g0125others(36): Show | 41 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.734-515C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298582 | ||||||
chrX:298584
|
A | G | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-513A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298584 | ||||||
chrX:298589
|
T | C | 2 | a0001c0001t0015g0074a0001c0003t0055g0010 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.734-508T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298589 | ||||||
chrX:298589
|
TCTGTCTA others(140): Show |
T | 1 | a0001c0002t0076g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.734-486_734-340del | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298589 | |||||
chrX:298596
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0018g0099a0001c0001t0018g0100others(4): Show | 8 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-501A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298596 | ||||||
chrX:298597
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0018g0099a0001c0001t0018g0100others(4): Show | 8 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-500T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298597 | ||||||
chrX:298600
|
CAT | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(53): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-496_734-495del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298600 | ||||||
chrX:298609
|
T | C | 1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-488T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298609 | ||||||
chrX:298611
|
C | CGACGTGG others(238): Show |
1 | a0001c0002t0094g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.734-320_734-319ins others(245): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298611 | |||||
chrX:298611
|
C | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0053others(105): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.734-486C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298611 | ||||||
chrX:298614
|
C | T | 9 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0001t0027g0059others(6): Show | 9 | HG01123.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-483C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298614 | ||||||
chrX:298615
|
G | A | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-482G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298615 | ||||||
chrX:298626
|
T | TG | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-467dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298626 | |||||
chrX:298626
|
TG | T | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-467delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298626 | |||||
chrX:298631
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0012g0015 | 3 | HG01070.hp1 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.734-466A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298631 | ||||||
chrX:298645
|
C | A | 21 | a0001c0001t0001g0003a0001c0001t0012g0015a0001c0001t0018g0099others(18): Show | 22 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-452C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298645 | ||||||
chrX:298646
|
C | CCACATGG others(2629): Show |
1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-443_734-442ins others(2636): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298646 | |||||
chrX:298646
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0012g0015a0001c0001t0018g0099others(18): Show | 22 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.734-451C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298646 | ||||||
chrX:298649
|
CAT | C | 1 | a0001c0001t0012g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-447_734-446del others(2): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298649 | ||||||
chrX:298652
|
G | T | 1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-445G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298652 | ||||||
chrX:298658
|
T | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0089g0011 | 3 | HG02559.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.734-439T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298658 | ||||||
chrX:298663
|
C | T | 1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-434C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298663 | ||||||
chrX:298680
|
A | ACATTATT others(2182): Show |
1 | a0002c0019t0022g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-391_734-390ins others(2189): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298680 | |||||
chrX:298680
|
A | C | 4 | a0001c0001t0018g0099a0001c0001t0018g0100a0001c0003t0055g0010others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-417A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298680 | ||||||
chrX:298682
|
A | G | 1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-415A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298682 | ||||||
chrX:298686
|
TTCTG | T | 1 | a0001c0003t0089g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.734-407_734-404del others(4): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298686 | |||||
chrX:298687
|
T | C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-410T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298687 | ||||||
chrX:298687
|
TCTGTCTA others(42): Show |
T | 77 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0054others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.734-390_734-342del others(49): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298687 | |||||
chrX:298690
|
G | GTCTCCCA others(87): Show |
1 | a0001c0002t0090g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-404_734-403ins others(94): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298690 | |||||
chrX:298694
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0012g0015 | 3 | HG01070.hp1 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.734-403A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298694 | ||||||
chrX:298695
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0012g0015 | 3 | HG01070.hp1 HG01071.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.734-402T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298695 | ||||||
chrX:298707
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0012g0015a0001c0001t0015g0074others(26): Show | 30 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-390C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298707 | ||||||
chrX:298729
|
C | A | 16 | a0001c0001t0001g0003a0001c0001t0012g0015a0001c0001t0018g0099others(13): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.734-368C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298729 | ||||||
chrX:298729
|
C | CCATTATT others(89): Show |
1 | a0001c0001t0012g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.734-362_734-361ins others(96): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298729 | |||||
chrX:298729
|
C | CTGTTATT others(189): Show |
1 | a0001c0001t0015g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.734-368_734-367ins others(196): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298729 | ||||||
chrX:298736
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0012g0015a0001c0001t0012g0149others(14): Show | 18 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.734-361C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298736 | ||||||
chrX:298743
|
A | C | 24 | a0001c0001t0009g0067a0001c0001t0011g0125a0001c0001t0011g0126others(21): Show | 25 | HG01123.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-354A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298743 | ||||||
chrX:298744
|
T | C | 24 | a0001c0001t0009g0067a0001c0001t0011g0125a0001c0001t0011g0126others(21): Show | 25 | HG01123.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-353T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298744 | ||||||
chrX:298746
|
A | ACATGGGG others(385): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-307_734-306ins others(392): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298746 | |||||
chrX:298761
|
C | CGTGGACA others(5457): Show |
1 | a0008c0011t0108g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-305_734-304ins others(5464): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298761 | |||||
chrX:298761
|
C | CGTGGACA others(8348): Show |
1 | a0001c0003t0023g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.734-282_734-281ins others(8355): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298761 | |||||
chrX:298761
|
C | CGTGGACA others(8299): Show |
1 | a0001c0003t0023g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.734-282_734-281ins others(8306): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298761 | |||||
chrX:298761
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 99 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.734-336C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298761 | ||||||
chrX:298773
|
T | TG | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-320dupG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298773 | |||||
chrX:298778
|
A | C | 1 | a0001c0003t0051g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-319A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298778 | ||||||
chrX:298805
|
T | C | 27 | a0001c0001t0009g0067a0001c0001t0011g0125a0001c0001t0011g0126others(24): Show | 28 | HG01123.hp1 HG01346.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.734-292T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298805 | ||||||
chrX:298810
|
C | CGTGGACA others(5212): Show |
1 | a0001c0003t0107g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-271_734-270ins others(5219): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298810 | |||||
chrX:298822
|
TG | T | 1 | a0001c0010t0042g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-271delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298822 | |||||
chrX:298827
|
C | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.734-270C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298827 | ||||||
chrX:298838
|
T | TC | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-258dupC | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298838 | |||||
chrX:298847
|
TG | T | 1 | a0000c0018t0101g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734-246delG | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 298847 | |||||
chrX:298859
|
T | C | 3 | a0001c0001t0027g0059a0001c0001t0052g0068a0001c0003t0065g0012 | 3 | HG01123.hp2 NA18964.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-238T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298859 | ||||||
chrX:298867
|
T | C | 3 | a0001c0001t0027g0059a0001c0001t0052g0068a0001c0003t0065g0012 | 3 | HG01123.hp2 NA18964.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.734-230T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298867 | ||||||
chrX:298929
|
T | C | 1 | a0001c0003t0058g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-168T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298929 |