Item | Value |
---|---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 323 | 166 | 32 | 32 | 85 | 5 | 10 | 68 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0002 | 0/0 | 323 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0003 | 0/0 | 323 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0004 | 0/0 | 214 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(209): Show |
chrX | 276381 | 308356 |
a0005 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0006 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0007 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
a0008 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | MGGQV others(318): Show |
chrX | 276381 | 308356 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 969 | 91 | 14 | 9 | 59 | 4 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0002 | 1/1 | 969 | 35 | 1 | 13 | 14 | 0 | 5 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0003 | 0/0 | 969 | 31 | 16 | 9 | 5 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0004 | 0/0 | 969 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0006 | 0/0 | 969 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0009 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0010 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0001c0014 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0002c0005 | 0/0 | 969 | 2 | 1 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0002c0016 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0003c0007 | 0/0 | 969 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0004c0012 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0005c0015 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0006c0011 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0007c0008 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 | ||
a0008c0013 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | ATGGG others(964): Show |
chrX | 276381 | 308356 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5320 | 11 | 0 | 3 | 6 | 2 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0002 | 0/0 | 5308 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0003 | 0/0 | 5320 | 6 | 0 | 0 | 6 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0004 | 0/0 | 5308 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0005 | 0/0 | 5320 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0007 | 0/0 | 5306 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0009 | 0/0 | 5320 | 3 | 0 | 2 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0010 | 0/0 | 5317 | 3 | 0 | 1 | 0 | 0 | 2 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5312): Show |
chrX | 276381 | 308356 |
a0001c0001t0011 | 0/0 | 5308 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0012 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5308): Show |
chrX | 276381 | 308356 |
a0001c0001t0013 | 0/0 | 5302 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5297): Show |
chrX | 276381 | 308356 |
a0001c0001t0014 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0015 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5316): Show |
chrX | 276381 | 308356 |
a0001c0001t0016 | 0/0 | 5317 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5312): Show |
chrX | 276381 | 308356 |
a0001c0001t0017 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0018 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0019 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0020 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5308): Show |
chrX | 276381 | 308356 |
a0001c0001t0021 | 0/0 | 5304 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0001t0022 | 0/0 | 5276 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5271): Show |
chrX | 276381 | 308356 |
a0001c0001t0028 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0029 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0030 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0031 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5316): Show |
chrX | 276381 | 308356 |
a0001c0001t0032 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0033 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5316): Show |
chrX | 276381 | 308356 |
a0001c0001t0034 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0001t0035 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0036 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0037 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5308): Show |
chrX | 276381 | 308356 |
a0001c0001t0040 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0043 | 0/0 | 5317 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5312): Show |
chrX | 276381 | 308356 |
a0001c0001t0044 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0047 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0001t0048 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0001t0052 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0058 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0001t0061 | 0/0 | 5319 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5314): Show |
chrX | 276381 | 308356 |
a0001c0001t0064 | 0/0 | 5319 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5314): Show |
chrX | 276381 | 308356 |
a0001c0001t0065 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5313): Show |
chrX | 276381 | 308356 |
a0001c0001t0066 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0001t0067 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5298): Show |
chrX | 276381 | 308356 |
a0001c0001t0068 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5313): Show |
chrX | 276381 | 308356 |
a0001c0001t0069 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5314): Show |
chrX | 276381 | 308356 |
a0001c0001t0070 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0071 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0001t0074 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5313): Show |
chrX | 276381 | 308356 |
a0001c0001t0075 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0001t0076 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0001t0078 | 0/0 | 5317 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5312): Show |
chrX | 276381 | 308356 |
a0001c0001t0079 | 0/0 | 5315 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5310): Show |
chrX | 276381 | 308356 |
a0001c0001t0081 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0001c0001t0082 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0001t0086 | 0/0 | 5310 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5305): Show |
chrX | 276381 | 308356 |
a0001c0001t0089 | 0/0 | 5305 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0001c0001t0093 | 0/0 | 5304 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0001t0097 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0002t0001 | 0/0 | 5320 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0002t0002 | 0/0 | 5308 | 5 | 0 | 1 | 2 | 0 | 2 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0003 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0002t0004 | 0/0 | 5308 | 4 | 0 | 1 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0008 | 0/0 | 5308 | 4 | 0 | 4 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0011 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0018 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0002t0023 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0002t0045 | 0/0 | 5308 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0046 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0002t0049 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0002t0050 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0002t0060 | 0/1 | 5320 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0002t0084 | 0/0 | 5316 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5311): Show |
chrX | 276381 | 308356 |
a0001c0002t0085 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0002t0087 | 0/0 | 5310 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5305): Show |
chrX | 276381 | 308356 |
a0001c0002t0088 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0002t0090 | 1/0 | 5318 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5313): Show |
chrX | 276381 | 308356 |
a0001c0002t0091 | 0/0 | 5308 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0092 | 0/0 | 5308 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0094 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0002t0095 | 0/0 | 5305 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0001c0002t0099 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5317): Show |
chrX | 276381 | 308356 |
a0001c0002t0103 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0003t0002 | 0/0 | 5308 | 5 | 0 | 2 | 3 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0003t0006 | 0/0 | 5304 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0003t0015 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5316): Show |
chrX | 276381 | 308356 |
a0001c0003t0017 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0003t0019 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0003t0024 | 0/0 | 5309 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0001c0003t0027 | 0/0 | 5305 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0001c0003t0038 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0003t0039 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5303): Show |
chrX | 276381 | 308356 |
a0001c0003t0042 | 0/0 | 5315 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5310): Show |
chrX | 276381 | 308356 |
a0001c0003t0051 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0003t0053 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0003t0054 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0003t0055 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0003t0056 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0001c0003t0057 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0003t0059 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0003t0063 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5316): Show |
chrX | 276381 | 308356 |
a0001c0003t0077 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0003t0080 | 0/0 | 5315 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5310): Show |
chrX | 276381 | 308356 |
a0001c0003t0083 | 0/0 | 5316 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5311): Show |
chrX | 276381 | 308356 |
a0001c0003t0098 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0003t0101 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0001c0004t0001 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0004t0007 | 0/0 | 5306 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0006t0003 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0001c0006t0072 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0009t0096 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0001c0010t0041 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0001c0014t0062 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0002c0005t0026 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0002c0005t0100 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0002c0016t0026 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5302): Show |
chrX | 276381 | 308356 |
a0003c0007t0023 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0003c0007t0025 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
a0004c0012t0005 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5315): Show |
chrX | 276381 | 308356 |
a0005c0015t0006 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5299): Show |
chrX | 276381 | 308356 |
a0006c0011t0102 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5300): Show |
chrX | 276381 | 308356 |
a0007c0008t0073 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5301): Show |
chrX | 276381 | 308356 |
a0008c0013t0025 | 0/0 | 5309 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | CTTCC others(5304): Show |
chrX | 276381 | 308356 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0042 | 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 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0003g0022 | 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 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0035 | 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 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0014g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0016g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0017g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0020g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0021g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0021g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0022g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0022g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0028g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0029g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0030g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0031g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0032g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0033g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0034g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0035g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0036g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0037g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0040g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0043g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0044g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0047g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0048g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0052g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0058g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0061g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0064g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0065g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0066g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0067g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0068g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0069g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0070g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0071g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0074g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0075g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0076g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0078g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0079g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0081g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0082g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0086g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0089g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0093g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0001t0097g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0008g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0011g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0023g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0045g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0046g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0049g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0050g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0060g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0084g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0085g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0087g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0088g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0090g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0091g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0092g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0094g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0095g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0099g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0002t0103g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0017g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0019g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0024g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0024g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0027g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0038g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0039g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0042g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0051g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0053g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0054g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0055g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0056g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0057g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0059g0050 | 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 |
a0001c0003t0077g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0080g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0083g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0098g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0003t0101g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0004t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0006t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0006t0072g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0009t0096g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0010t0041g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0001c0014t0062g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0005t0026g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0005t0100g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0002c0016t0026g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0003c0007t0023g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0003c0007t0025g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0004c0012t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0005c0015t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0006c0011t0102g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0007c0008t0073g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
a0008c0013t0025g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | t0017 | g0048 | EUR | GBR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00280 | hp1 | a0001 | c0001 | t0089 | g0096 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00323 | hp2 | a0001 | c0001 | t0069 | g0043 | EUR | FIN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00408 | hp1 | a0001 | c0001 | t0016 | g0002 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00408 | hp2 | a0001 | c0001 | t0061 | g0166 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00423 | hp1 | a0001 | c0001 | t0064 | g0036 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00423 | hp2 | a0001 | c0001 | t0011 | g0091 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00438 | hp1 | a0001 | c0001 | t0014 | g0028 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00544 | hp1 | a0003 | c0007 | t0025 | g0006 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00544 | hp2 | a0001 | c0001 | t0019 | g0090 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00558 | hp1 | a0003 | c0007 | t0023 | g0006 | 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 | t0047 | g0023 | EAS | CHS | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00639 | hp1 | a0002 | c0016 | t0026 | g0148 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00639 | hp2 | a0001 | c0002 | t0008 | g0162 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00735 | hp1 | a0002 | c0005 | t0026 | g0031 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00735 | hp2 | a0001 | c0001 | t0028 | g0066 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG00738 | hp1 | a0001 | c0002 | t0087 | g0147 | 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 | t0024 | g0058 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0137 | 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 | t0024 | g0033 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0040 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01168 | hp2 | a0001 | c0003 | t0059 | g0050 | AMR | PUR | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0013 | 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 | t0094 | g0001 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01346 | hp1 | a0001 | c0014 | t0062 | g0094 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0097 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01361 | hp1 | a0001 | c0002 | t0008 | g0124 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01361 | hp2 | a0001 | c0001 | t0067 | g0052 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0070 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01496 | hp2 | a0001 | c0003 | t0039 | g0005 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01891 | hp1 | a0001 | c0003 | t0006 | g0120 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01891 | hp2 | a0001 | c0001 | t0081 | g0061 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01943 | hp2 | a0001 | c0002 | t0011 | g0001 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01975 | hp1 | a0001 | c0002 | t0103 | g0141 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01975 | hp2 | a0001 | c0002 | t0004 | g0140 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01993 | hp1 | a0001 | c0002 | t0095 | g0139 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02056 | hp1 | a0001 | c0001 | t0031 | g0014 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02080 | hp2 | a0001 | c0001 | t0011 | g0129 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02148 | hp1 | a0001 | c0002 | t0008 | g0138 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0068 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02155 | hp1 | a0001 | c0006 | t0003 | g0126 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02155 | hp2 | a0001 | c0001 | t0044 | g0024 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02165 | hp1 | a0004 | c0012 | t0005 | g0045 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | CDX | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02257 | hp1 | a0002 | c0005 | t0100 | g0079 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02257 | hp2 | a0001 | c0003 | t0055 | g0007 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02280 | hp1 | a0001 | c0003 | t0056 | g0086 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0074 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02293 | hp1 | a0001 | c0002 | t0008 | g0123 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02293 | hp2 | a0001 | c0003 | t0038 | g0005 | AMR | PEL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02615 | hp1 | a0001 | c0003 | t0053 | g0105 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02615 | hp2 | a0001 | c0003 | t0051 | g0076 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02622 | hp1 | a0001 | c0003 | t0057 | g0104 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02622 | hp2 | a0001 | c0001 | t0022 | g0101 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02630 | hp1 | a0005 | c0015 | t0006 | g0078 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02630 | hp2 | a0006 | c0011 | t0102 | g0017 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0133 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02683 | hp1 | a0001 | c0002 | t0091 | g0150 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02683 | hp2 | a0001 | c0002 | t0092 | g0146 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02723 | hp1 | a0007 | c0008 | t0073 | g0073 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02723 | hp2 | a0001 | c0003 | t0027 | g0015 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02886 | hp1 | a0001 | c0001 | t0021 | g0107 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02886 | hp2 | a0001 | c0003 | t0027 | g0016 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02896 | hp1 | a0001 | c0001 | t0079 | g0106 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02896 | hp2 | a0001 | c0003 | t0080 | g0157 | AFR | GWD | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02922 | hp1 | a0001 | c0002 | t0084 | g0156 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02922 | hp2 | a0001 | c0003 | t0006 | g0039 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0010 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03017 | hp1 | a0001 | c0001 | t0010 | g0089 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0108 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03130 | hp1 | a0001 | c0003 | t0101 | g0109 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03139 | hp1 | a0001 | c0003 | t0042 | g0121 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03195 | hp1 | a0001 | c0001 | t0022 | g0100 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03195 | hp2 | a0001 | c0003 | t0006 | g0038 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03486 | hp1 | a0001 | c0001 | t0037 | g0062 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03486 | hp2 | a0001 | c0003 | t0098 | g0087 | AFR | MSL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03516 | hp1 | a0001 | c0001 | t0082 | g0060 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0154 | AFR | ESN | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0143 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03669 | hp2 | a0008 | c0013 | t0025 | g0155 | SAS | PJL | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03927 | hp1 | a0001 | c0002 | t0088 | g0149 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG03927 | hp2 | a0001 | c0001 | t0078 | g0093 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04184 | hp1 | a0001 | c0001 | t0017 | g0099 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04184 | hp2 | a0001 | c0001 | t0086 | g0088 | SAS | BEB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0083 | SAS | STU | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0145 | SAS | STU | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | CHB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18906 | hp1 | a0001 | c0003 | t0054 | g0085 | AFR | YRI | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18906 | hp2 | a0001 | c0010 | t0041 | g0167 | AFR | YRI | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18941 | hp1 | a0001 | c0001 | t0036 | g0071 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18941 | hp2 | a0001 | c0002 | t0050 | g0159 | 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 | t0001 | g0115 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18944 | hp1 | a0001 | c0002 | t0046 | g0001 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18947 | hp1 | a0001 | c0004 | t0007 | g0116 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18947 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18948 | hp1 | a0001 | c0001 | t0032 | g0063 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18950 | hp1 | a0001 | c0001 | t0074 | g0082 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18950 | hp2 | a0001 | c0001 | t0075 | g0044 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18951 | hp1 | a0001 | c0004 | t0007 | g0117 | 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 | g0051 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18954 | hp2 | a0001 | c0009 | t0096 | g0027 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18961 | hp1 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18964 | hp2 | a0001 | c0001 | t0052 | g0072 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18969 | hp1 | a0001 | c0001 | t0034 | g0067 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18969 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18980 | hp1 | a0001 | c0001 | t0040 | g0065 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18980 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18985 | hp1 | a0001 | c0002 | t0004 | g0112 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18986 | hp1 | a0001 | c0003 | t0019 | g0032 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18988 | hp1 | a0001 | c0002 | t0023 | g0142 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18991 | hp1 | a0001 | c0001 | t0071 | g0168 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18991 | hp2 | a0001 | c0001 | t0065 | g0029 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18992 | hp1 | a0001 | c0001 | t0015 | g0055 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0165 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18993 | hp1 | a0001 | c0001 | t0018 | g0102 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18993 | hp2 | a0001 | c0006 | t0072 | g0114 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18998 | hp1 | a0001 | c0001 | t0093 | g0132 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18999 | hp1 | a0001 | c0001 | t0097 | g0034 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19003 | hp1 | a0001 | c0003 | t0077 | g0164 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19003 | hp2 | a0001 | c0002 | t0085 | g0158 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19006 | hp1 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19009 | hp1 | a0001 | c0001 | t0029 | g0059 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19011 | hp1 | a0001 | c0001 | t0048 | g0047 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19011 | hp2 | a0001 | c0001 | t0030 | g0064 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19055 | hp1 | a0001 | c0002 | t0018 | g0111 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19056 | hp1 | a0001 | c0001 | t0066 | g0153 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19057 | hp2 | a0001 | c0001 | t0035 | g0080 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19060 | hp1 | a0001 | c0001 | t0070 | g0152 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19062 | hp1 | a0001 | c0001 | t0014 | g0119 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19063 | hp1 | a0001 | c0001 | t0033 | g0069 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19074 | hp1 | a0001 | c0001 | t0076 | g0092 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19074 | hp2 | a0001 | c0001 | t0068 | g0103 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19080 | hp1 | a0001 | c0002 | t0045 | g0001 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19081 | hp2 | a0001 | c0002 | t0049 | g0018 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19086 | hp1 | a0001 | c0002 | t0099 | g0135 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19090 | hp1 | a0001 | c0001 | t0058 | g0130 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01123 | hp1 | a0001 | c0001 | t0043 | g0012 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG01123 | hp2 | a0001 | c0003 | t0015 | g0009 | AMR | CLM | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02559 | hp1 | a0001 | c0003 | t0083 | g0008 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0075 | AFR | ACB | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
homoSapiens | chm13v2 | a0001 | c0002 | t0060 | g0161 | REF | REF | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
homoSapiens | grch38p0 | a0001 | c0002 | t0090 | g0127 | REF | REF | PLCXD1_chrX_276381_308356 | PLCXD1 | chrX | 276381 | 308356 |
view | 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:284275 | C | T | 1 | a0005 | 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:291610 | G | A | 1 | a0007 | 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 | a0004 | 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 | a0008 | 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 | a0006 | 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 |
view | 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 | 11 | a0001c0001 a0001c0003 a0001c0009 others(8): 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 | 5 | a0001c0001 a0001c0006 a0001c0014 others(2): 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 | 2 | a0001c0004 a0001c0014 |
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 |
view | 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:281411 | T | C | 14 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0029 others(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:299379 | C | G | 1 | a0001c0002t0103 | 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 | a0001c0010t0041 | 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 | a0001c0001t0012 a0001c0001t0043 a0001c0003t0042 |
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 | a0001c0001t0044 | 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 | a0001c0010t0041 | 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 | 10 | a0001c0001t0004 a0001c0001t0028 a0001c0001t0047 others(7): 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:299587 | A | G | 6 | a0001c0003t0027 a0001c0003t0101 a0002c0005t0026 others(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:299629 | C | T | 1 | a0001c0002t0099 | 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 | a0001c0003t0027 a0001c0003t0101 a0002c0005t0026 others(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 | a0001c0003t0098 | 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:299771 | C | A | 10 | a0001c0001t0029 a0001c0001t0052 a0001c0003t0006 others(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 | a0001c0003t0057 | 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 | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): 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 | a0001c0003t0027 a0001c0003t0057 a0001c0003t0101 others(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 | a0001c0001t0019 a0001c0001t0078 a0001c0003t0019 others(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 | 63 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(60): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): 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 | 63 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(60): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): 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 | 62 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(59): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(88): 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 | 78 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(75): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): 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 | a0001c0002t0045 a0001c0002t0046 |
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 | a0001c0001t0030 | 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 | a0001c0003t0027 a0006c0011t0102 |
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 | a0001c0001t0019 a0001c0003t0019 a0001c0003t0077 |
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 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0058 others(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 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(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 | a0001c0003t0027 a0001c0003t0101 a0002c0005t0026 others(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: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 | a0001c0001t0017 a0001c0001t0067 a0001c0003t0017 |
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 | a0001c0001t0012 a0001c0001t0020 a0001c0001t0021 others(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 | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
71 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 908 | chrX | 300243 | ||||||
chrX:300396 | GTGTC | G | 3 | a0001c0001t0020 a0001c0001t0037 a0001c0001t0079 |
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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0054 others(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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0054 others(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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0054 others(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 | 67 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(64): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): 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 | a0002c0005t0026 a0002c0005t0100 a0002c0016t0026 |
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 | a0001c0001t0019 a0001c0001t0047 a0001c0002t0023 others(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 | a0001c0001t0012 | 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 | a0001c0001t0022 | 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 | 73 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(70): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 1135 | chrX | 300470 | ||||||
chrX:300482 | ATGTG | A | 4 | a0001c0001t0089 a0002c0005t0026 a0002c0005t0100 others(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 | a0001c0001t0022 | 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 | a0001c0001t0013 | 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 | a0001c0001t0066 | 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:300504 | GTA | G | 19 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(16): 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:300508 | A | G | 2 | a0001c0001t0022 a0001c0001t0052 |
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 | a0001c0002t0094 | 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 | 4 | a0001c0001t0003 a0001c0001t0064 a0001c0002t0003 others(1): 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 | a0001c0002t0087 | 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 | a0001c0001t0022 | 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 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(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 | a0001c0001t0010 | 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 | a0001c0001t0019 a0001c0001t0029 a0001c0001t0052 |
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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0054 others(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 | a0001c0001t0021 a0001c0001t0067 a0001c0001t0081 others(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 | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(55): Show |
89 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(86): 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 | a0002c0005t0026 a0002c0005t0100 a0002c0016t0026 |
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 | a0001c0001t0013 | 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 | a0001c0001t0022 | 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 | a0001c0001t0035 | 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 | a0001c0003t0042 | 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 | a0001c0003t0027 a0001c0003t0051 |
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 | 14 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0020 others(11): 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 | a0001c0001t0005 a0001c0001t0074 a0004c0012t0005 |
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:300795 | C | T | 1 | a0001c0001t0013 | 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 | a0001c0003t0077 | 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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0022 others(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 | a0001c0001t0013 | 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 | a0001c0001t0029 a0001c0001t0052 |
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 | a0001c0001t0013 | 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 | a0001c0001t0021 | 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 | a0001c0010t0041 | 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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(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 | a0001c0001t0013 | 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 | a0001c0001t0021 a0001c0001t0081 a0001c0001t0082 |
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 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0081 others(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 | 49 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(46): 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 | a0001c0001t0021 a0001c0001t0081 a0001c0001t0082 |
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 | a0001c0001t0021 a0001c0001t0081 a0001c0001t0082 |
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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0054 others(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 | a0001c0003t0098 | 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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | 75 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(72): 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:301464 | G | A | 11 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0081 others(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 | a0001c0001t0081 a0001c0001t0082 |
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 | a0001c0003t0098 | 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 | a0001c0001t0032 | 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 | a0001c0003t0038 a0001c0003t0039 |
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 | a0001c0001t0013 a0001c0003t0057 a0001c0003t0098 |
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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | 19 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0028 others(16): 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 | 76 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(73): 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 | 112 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(109): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*2672A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 7/7 | 2672 | chrX | 302007 | ||||||
chrX:302110 | A | G | 21 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0021 others(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 | a0001c0002t0091 | 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 | a0001c0001t0013 | 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 | a0001c0001t0013 | 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 | 75 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(72): 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 | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): 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 | a0001c0001t0015 a0001c0001t0071 a0001c0001t0086 others(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 | AC | A | 24 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(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:302314 | G | A | 1 | a0001c0003t0083 | 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 | a0001c0003t0054 a0001c0003t0056 |
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 | 4 | a0001c0001t0010 a0001c0001t0078 a0001c0002t0084 others(1): 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 | 54 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(51): 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:302483 | T | C | 5 | a0001c0002t0008 a0001c0002t0094 a0001c0002t0095 others(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:302590 | G | C | 56 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(53): 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 | 56 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(53): 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 | a0001c0003t0038 | 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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(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 | a0001c0002t0092 | 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 | a0001c0001t0018 a0001c0002t0018 |
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:302965 | C | A | 19 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0029 others(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 | a0006c0011t0102 a0007c0008t0073 |
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 | a0001c0003t0101 | 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 | a0001c0003t0006 a0001c0003t0053 a0001c0003t0055 others(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 | a0001c0001t0033 a0001c0001t0058 a0001c0001t0075 others(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 | a0001c0003t0024 | 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 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0035 others(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 | 58 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(55): 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 |
view | 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:281735 | C | G | 1 | a0001c0001t0071g0168 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+51C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281735 | |||||||
chrX:281767 | C | G | 1 | a0001c0010t0041g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22+83C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281767 | |||||||
chrX:281791 | C | T | 3 | a0001c0001t0061g0166 a0001c0003t0002g0165 a0001c0003t0077g0164 |
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 | a0001c0003t0015g0009 a0001c0003t0055g0007 a0001c0003t0083g0008 |
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:281825 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(109): 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 | a0001c0001t0004g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+141T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 281825 | |||||||
chrX:282042 | C | T | 6 | a0001c0001t0021g0107 a0001c0001t0021g0108 a0001c0003t0015g0009 others(3): 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:282045 | G | T | 1 | a0001c0001t0079g0106 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-22+361G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282045 | |||||||
chrX:282229 | A | C | 1 | a0001c0001t0004g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22+545A>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282229 | |||||||
chrX:282280 | G | T | 2 | a0001c0003t0053g0105 a0001c0003t0057g0104 |
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 | a0001c0003t0057g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22+630G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282314 | |||||||
chrX:282392 | C | A | 1 | a0001c0003t0057g0104 | 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 | a0001c0001t0013g0010 a0001c0003t0057g0104 |
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 | a0001c0001t0013g0010 a0001c0003t0053g0105 |
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 | CA | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(79): 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:282405 | A | C | 1 | a0001c0003t0053g0105 | 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 | 22 | a0001c0001t0001g0084 a0001c0001t0001g0163 a0001c0001t0005g0095 others(19): Show |
22 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(19): 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 | a0001c0001t0068g0103 | 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 | a0001c0001t0005g0081 a0001c0001t0074g0082 |
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:282510 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:282537 | T | C | 1 | a0001c0001t0071g0168 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+853T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282537 | |||||||
chrX:282631 | G | C | 1 | a0001c0001t0013g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-22+947G>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282631 | |||||||
chrX:282703 | C | CA | 38 | a0001c0001t0001g0084 a0001c0001t0003g0019 a0001c0001t0003g0020 others(35): 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 | CA | C | 6 | a0001c0001t0035g0080 a0001c0002t0001g0160 a0001c0002t0049g0018 others(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:282741 | A | T | 2 | a0002c0005t0100g0079 a0005c0015t0006g0078 |
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 | a0001c0003t0080g0157 | 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 | a0001c0009t0096g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-22+1068G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 282752 | |||||||
chrX:282805 | C | T | 2 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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:282836 | T | C | 5 | a0001c0004t0001g0115 a0001c0004t0001g0118 a0001c0004t0007g0116 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0005g0098 others(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 | 23 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0084 others(20): 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:282892 | T | C | 3 | a0001c0001t0013g0010 a0002c0005t0100g0079 a0005c0015t0006g0078 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0001c0003t0057g0104 a0001c0009t0096g0027 |
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 | a0001c0001t0013g0010 a0001c0003t0053g0105 a0002c0005t0100g0079 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0005g0098 others(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 | 32 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0077 others(29): 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0057g0104 | 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 | a0001c0001t0079g0106 | 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:283048 | T | C | 2 | a0001c0001t0014g0028 a0001c0001t0065g0029 |
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 | a0001c0001t0013g0154 a0001c0001t0071g0168 a0008c0013t0025g0155 |
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 | a0001c0001t0009g0077 a0001c0003t0006g0120 a0001c0003t0042g0121 |
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 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0020g0074 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | 10 | a0001c0001t0013g0010 a0001c0001t0021g0107 a0001c0001t0021g0108 others(7): 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:283129 | G | A | 1 | a0001c0003t0057g0104 | 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 | a0001c0001t0010g0083 | 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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(80): 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 | a0001c0001t0001g0084 a0001c0001t0003g0030 a0001c0001t0005g0095 others(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:283274 | C | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0002c0005t0100g0079 a0005c0015t0006g0078 |
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:283500 | T | G | 2 | a0002c0005t0100g0079 a0005c0015t0006g0078 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0013g0010 | 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 | a0001c0003t0006g0120 a0001c0003t0042g0121 |
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 | a0001c0001t0037g0062 | 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 | a0001c0001t0081g0061 a0001c0001t0082g0060 |
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:283536 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 |
2 | a0001c0001t0021g0107 a0001c0001t0021g0108 |
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 | a0001c0001t0013g0010 | 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 | a0001c0003t0019g0032 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0002c0005t0100g0079 a0005c0015t0006g0078 |
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 | 2 | a0001c0001t0021g0107 a0001c0001t0021g0108 |
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 | a0001c0003t0101g0109 | 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:283591 | C | G | 1 | a0001c0002t0004g0122 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:283598 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0006c0011t0102g0017 | 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 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0079g0106 others(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 | a0001c0002t0004g0122 | 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 | a0001c0002t0004g0122 | 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 | a0001c0004t0007g0116 a0001c0004t0007g0117 |
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 | a0001c0002t0004g0125 | 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 | a0001c0001t0081g0061 a0001c0001t0082g0060 a0001c0002t0004g0125 others(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 | a0001c0002t0004g0125 a0001c0003t0019g0032 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0001c0003t0053g0105 others(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:283654 | T | TCAGGCAC others(273): Show |
1 | a0001c0002t0004g0125 | 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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0002t0004g0112 a0001c0002t0045g0001 a0001c0002t0046g0001 |
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 | a0001c0001t0013g0154 | 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 | a0001c0003t0019g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-21-506C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 1/6 | chrX | 283661 | |||||||
chrX:283688 | A | ACGGGTGG others(301): Show |
1 | a0001c0001t0030g0064 | 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 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0077 others(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:283715 | A | G | 2 | a0001c0001t0081g0061 a0001c0001t0082g0060 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0003t0057g0104 | 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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(106): 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:283878 | CT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(87): 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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0074g0082 |
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:284470 | CACAT | C | 2 | a0001c0003t0024g0033 a0001c0003t0024g0058 |
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 | a0001c0006t0003g0126 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | 74 | a0001c0001t0007g0128 a0001c0001t0007g0131 a0001c0001t0009g0068 others(71): Show |
74 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(71): 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 | 16 | a0001c0001t0013g0010 a0001c0001t0020g0074 a0001c0001t0020g0075 others(13): 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 | a0001c0001t0070g0152 a0001c0001t0071g0168 |
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 | a0001c0001t0010g0097 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0037g0062 | 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 | a0001c0001t0037g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+315C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 284629 | |||||||
chrX:284640 | A | G | 3 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0074g0082 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(85): 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:285046 | G | A | 17 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0001t0005g0035 a0001c0001t0097g0034 |
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:285135 | T | C | 1 | a0001c0001t0043g0012 | 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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(125): 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 | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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:285279 | C | A | 1 | a0001c0001t0079g0106 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127+965C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285279 | |||||||
chrX:285341 | CACACGTG others(1): Show |
C | 2 | a0001c0001t0021g0107 a0001c0001t0021g0108 |
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 | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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 | 2 | a0001c0001t0021g0107 a0001c0001t0021g0108 |
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 | a0001c0001t0089g0096 | 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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:285556 | T | A | 2 | a0001c0002t0003g0136 a0001c0002t0099g0135 |
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 | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(113): 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 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0077 others(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:285660 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.127+1346C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 285660 | |||||||
chrX:285670 | C | T | 19 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(110): 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:285772 | T | C | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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:285791 | T | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(85): 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:285996 | C | T | 2 | a0001c0003t0057g0104 a0001c0003t0080g0157 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | 9 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(6): 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:286115 | A | G | 1 | a0001c0003t0080g0157 | 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 | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(110): 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 | a0001c0001t0064g0036 | 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 | a0001c0001t0005g0095 | 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 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0077 others(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:286248 | A | T | 4 | a0001c0001t0004g0025 a0001c0001t0004g0110 a0001c0001t0044g0024 others(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:286478 | G | A | 8 | a0001c0001t0007g0128 a0001c0001t0007g0131 a0001c0001t0011g0129 others(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 | a0001c0001t0030g0064 | 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 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0077 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0001t0067g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.128-2029C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 286704 | |||||||
chrX:286944 | G | C | 1 | a0001c0003t0080g0157 | 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 | a0001c0001t0010g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-1652T>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287081 | |||||||
chrX:287172 | TACAC | T | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0037g0062 others(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 | a0001c0001t0081g0061 a0001c0001t0082g0060 |
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 | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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:287334 | CATA | C | 17 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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:287442 | CACTATAT others(79): Show |
C | 10 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(7): 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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0002t0103g0141 | 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 | a0001c0001t0019g0090 a0001c0002t0001g0160 a0001c0002t0088g0149 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0001t0081g0061 others(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:287497 | G | T | 1 | a0001c0003t0101g0109 | 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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:287540 | TTATATAT others(84): Show |
T | 2 | a0001c0003t0053g0105 a0001c0003t0080g0157 |
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 | a0001c0003t0051g0076 | 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 | a0001c0002t0002g0145 | 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0037g0062 others(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:287569 | TTATATAT others(55): Show |
T | 7 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(64): 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 | a0001c0002t0008g0123 | 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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | 14 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0007g0128 others(11): 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 | a0001c0003t0042g0121 | 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 | a0001c0003t0042g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-1073G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287660 | |||||||
chrX:287679 | C | G | 20 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0021g0107 others(17): 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:287728 | C | CATATATA others(8): Show |
1 | a0001c0001t0067g0052 | 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 | a0001c0003t0057g0104 | 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:287836 | C | T | 1 | a0001c0001t0003g0022 | 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 | 3 | a0001c0001t0021g0107 a0001c0001t0021g0108 a0001c0002t0084g0156 |
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 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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:287903 | A | C | 3 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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:287973 | C | T | 5 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0002t0085g0158 | 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 | a0001c0002t0085g0158 | 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 | a0001c0003t0080g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.128-742G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 287991 | |||||||
chrX:288077 | A | ATCTCCAC others(322): Show |
6 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0037g0062 others(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:288133 | A | G | 2 | a0001c0002t0002g0113 a0001c0002t0002g0151 |
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:288234 | G | GCAGGGGG others(322): Show |
3 | a0001c0001t0021g0107 a0001c0001t0021g0108 a0001c0002t0084g0156 |
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 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0079g0106 others(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:288356 | G | C | 1 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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:288421 | C | T | 1 | a0001c0003t0057g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-312C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 2/6 | chrX | 288421 | |||||||
chrX:288633 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:288706 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0079g0106 others(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:289027 | A | C | 1 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0001t0061g0166 a0001c0003t0002g0165 a0001c0003t0077g0164 |
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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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:289254 | A | T | 1 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0001t0003g0021 | 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 | a0001c0001t0003g0021 | 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 | a0001c0001t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.264+498G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 289367 | |||||||
chrX:289392 | T | C | 9 | a0001c0003t0015g0009 a0001c0003t0027g0015 a0001c0003t0027g0016 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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:289516 | C | CT | 18 | a0001c0001t0003g0026 a0001c0001t0013g0010 a0001c0001t0013g0154 others(15): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0003g0020 a0001c0002t0091g0150 a0001c0003t0015g0009 others(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 | T | 17 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(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:289549 | C | T | 2 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0037g0062 others(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:289656 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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:289735 | A | G | 9 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0037g0062 others(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:289770 | C | A | 1 | a0001c0004t0001g0118 | 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 | a0001c0002t0003g0136 a0001c0002t0099g0135 a0003c0007t0023g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 |
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 | 21 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(18): 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 | a0001c0001t0052g0072 | 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 | 22 | a0001c0001t0001g0084 a0001c0001t0005g0095 a0001c0001t0010g0083 others(19): 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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:289970 | C | G | 7 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0037g0062 others(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:290095 | C | G | 1 | a0001c0010t0041g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.265-553C>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290095 | |||||||
chrX:290140 | A | C | 2 | a0001c0003t0051g0076 a0001c0003t0057g0104 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0012g0133 a0001c0001t0012g0134 |
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 | a0001c0001t0012g0133 a0001c0001t0012g0134 |
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 | a0001c0001t0081g0061 | 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 | a0001c0002t0087g0147 a0001c0002t0092g0146 |
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 | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(100): 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:290202 | T | C | 1 | a0002c0005t0100g0079 | 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 | 29 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0020g0074 others(26): 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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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 | 12 | a0001c0001t0021g0107 a0001c0001t0021g0108 a0001c0001t0022g0100 others(9): 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0017g0048 others(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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0017g0048 others(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:290290 | C | T | 19 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0007g0128 others(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:290298 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(117): 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 | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(114): 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 | a0001c0002t0002g0145 a0001c0003t0002g0011 a0001c0003t0019g0032 others(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 | a0001c0001t0005g0035 a0001c0001t0097g0034 |
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 | 35 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0007g0128 others(32): 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0022g0100 others(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:290407 | G | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(72): 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 | a0001c0001t0012g0133 a0001c0001t0012g0134 |
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:290417 | G | A | 3 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0007c0008t0073g0073 |
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 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0007g0128 others(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 | CA | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:290448 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-200C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290448 | |||||||
chrX:290538 | C | T | 1 | a0001c0002t0002g0145 | 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 | a0001c0002t0084g0156 a0001c0003t0002g0013 a0001c0003t0002g0040 others(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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 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 | a0001c0004t0001g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-74C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 3/6 | chrX | 290574 | |||||||
chrX:290784 | C | T | 56 | a0001c0001t0001g0084 a0001c0001t0005g0035 a0001c0001t0005g0095 others(53): 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 | a0001c0003t0053g0105 | 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 | a0001c0003t0053g0105 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+28T>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 4/6 | chrX | 290804 | |||||||
chrX:290813 | TGGGAGGC others(55): Show |
T | 8 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0081g0061 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0004g0110 | 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 | a0001c0003t0015g0009 | 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 | a0001c0003t0002g0013 a0001c0003t0002g0040 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0003t0053g0105 | 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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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:290882 | CGGCCGGG others(117): Show |
C | 1 | a0007c0008t0073g0073 | 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 | 2 | a0001c0001t0021g0107 a0001c0001t0021g0108 |
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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0003t0053g0105 others(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:290908 | C | G | 1 | a0001c0004t0001g0118 | 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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0003t0053g0105 | 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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0004t0001g0115 a0001c0004t0001g0118 a0001c0004t0007g0116 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0029g0059 others(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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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:290997 | G | A | 2 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0005t0100g0079 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 |
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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0003t0006g0038 others(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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0005t0100g0079 others(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 | a0001c0001t0031g0014 a0001c0002t0003g0136 a0001c0003t0006g0038 others(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:291180 | G | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:291331 | A | G | 2 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0003t0006g0038 others(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:291398 | G | A | 2 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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:291719 | A | G | 28 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0022g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0003t0019g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.549+126G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 291780 | |||||||
chrX:291997 | G | C | 29 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0020g0074 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0003t0027g0015 others(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 | a0001c0001t0019g0090 | 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 | a0001c0002t0088g0149 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0002t0084g0156 others(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 | a0001c0002t0091g0150 | 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 | a0001c0001t0022g0101 a0001c0003t0055g0007 a0001c0003t0057g0104 others(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 | a0001c0001t0014g0119 | 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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0014g0119 | 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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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 | a0001c0001t0004g0110 | 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 | a0001c0001t0011g0129 | 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 | a0001c0001t0003g0026 | 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 | a0001c0002t0099g0135 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:292495 | T | C | 2 | a0001c0001t0013g0010 a0001c0001t0013g0154 |
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 | a0001c0003t0055g0007 a0001c0003t0083g0008 |
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 | a0007c0008t0073g0073 | 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 | a0001c0001t0097g0034 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.550-259C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 5/6 | chrX | 292776 | |||||||
chrX:292886 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0003t0051g0076 | 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 | a0001c0003t0051g0076 | 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 | a0003c0007t0023g0006 a0003c0007t0025g0006 |
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 | a0001c0002t0084g0156 a0001c0003t0002g0013 a0001c0003t0002g0040 others(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 | a0001c0002t0002g0144 a0005c0015t0006g0078 |
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 | a0001c0001t0013g0154 | 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 | a0001c0002t0050g0159 | 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 | a0001c0001t0048g0047 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0086g0088 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0003t0051g0076 | 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 | a0001c0003t0054g0085 a0001c0003t0056g0086 |
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 | a0001c0003t0098g0087 | 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 | a0001c0001t0001g0084 a0001c0001t0005g0035 a0001c0001t0005g0081 others(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 | a0001c0001t0067g0052 | 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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0010t0041g0167 | 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 | a0001c0004t0007g0117 | 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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0031g0014 others(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 | a0001c0003t0051g0076 a0001c0003t0057g0104 |
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 | a0001c0010t0041g0167 | 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 | a0001c0001t0048g0047 a0001c0003t0051g0076 a0001c0003t0057g0104 |
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 | a0001c0003t0051g0076 a0001c0003t0057g0104 |
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 | a0001c0003t0051g0076 a0001c0003t0057g0104 |
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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0002t0084g0156 a0001c0003t0083g0008 |
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 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
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 | a0001c0003t0098g0087 | 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 | a0001c0001t0029g0059 a0001c0001t0035g0080 a0001c0001t0036g0071 others(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 | a0001c0001t0009g0077 | 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 | a0001c0003t0080g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.733+1236C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 294454 | |||||||
chrX:294481 | CA | C | 15 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0070g0152 others(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 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0003t0006g0038 others(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 | a0001c0002t0008g0123 a0001c0002t0008g0138 a0001c0002t0095g0139 |
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 | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(56): 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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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:294870 | G | A | 13 | a0001c0001t0012g0133 a0001c0001t0012g0134 a0001c0001t0013g0010 others(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 | a0001c0003t0002g0013 a0001c0003t0002g0040 |
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:295049 | A | G | 31 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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:295063 | G | A | 5 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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:295257 | A | G | 1 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.733+2039A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295257 | |||||||
chrX:295330 | C | T | 2 | a0001c0001t0081g0061 a0001c0001t0082g0060 |
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:295353 | G | A | 1 | a0008c0013t0025g0155 | 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 | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(103): 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:295406 | C | T | 1 | a0001c0002t0049g0018 | 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 | a0001c0001t0007g0128 a0001c0001t0007g0131 a0001c0001t0010g0083 others(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 | a0001c0010t0041g0167 | 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 | a0001c0001t0043g0012 | 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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(80): 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 | CT | C | 26 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0022g0100 others(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 | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(108): 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:295586 | G | A | 2 | a0001c0003t0042g0121 a0001c0003t0080g0157 |
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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0010t0041g0167 | 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 | a0001c0010t0041g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+2456G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 295674 | |||||||
chrX:295718 | A | G | 18 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0022g0100 others(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:295737 | C | T | 3 | a0001c0001t0081g0061 a0001c0001t0082g0060 a0001c0002t0099g0135 |
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:295927 | G | A | 3 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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:295945 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(91): 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:295955 | C | T | 13 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0029g0059 others(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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(80): 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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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 | a0001c0001t0020g0074 a0001c0001t0020g0075 a0001c0001t0079g0106 |
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:296075 | G | C | 6 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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:296122 | T | A | 1 | a0001c0001t0010g0097 | 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 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0015g0009 others(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:296279 | C | A | 1 | a0002c0016t0026g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.734-2818C>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296279 | |||||||
chrX:296280 | T | A | 1 | a0001c0002t0099g0135 | 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 | 20 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(17): 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 | a0001c0002t0099g0135 | 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 | a0001c0002t0099g0135 | 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 | a0001c0003t0057g0104 | 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 | a0001c0002t0099g0135 | 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 | a0001c0003t0015g0009 a0001c0003t0101g0109 a0002c0005t0026g0031 others(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:296369 | G | A | 1 | a0001c0003t0057g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-2728G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296369 | |||||||
chrX:296398 | C | T | 1 | a0001c0001t0058g0130 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.734-2699C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296398 | |||||||
chrX:296433 | T | G | 1 | a0001c0010t0041g0167 | 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 | a0001c0001t0029g0059 | 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 | 22 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(19): 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 | a0001c0003t0015g0009 a0001c0003t0101g0109 a0002c0005t0026g0031 others(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 | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(113): 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:296560 | T | C | 8 | a0001c0003t0015g0009 a0001c0003t0027g0015 a0001c0003t0027g0016 others(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 | a0001c0002t0099g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.734-2490A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296607 | |||||||
chrX:296635 | C | T | 1 | a0001c0003t0051g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734-2462C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 296635 | |||||||
chrX:296759 | A | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(113): 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 | a0001c0001t0047g0023 | 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:296832 | A | G | 25 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(22): 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:296856 | C | CATCTTTG others(532): Show |
3 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0029g0059 others(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 | a0001c0003t0101g0109 a0002c0005t0026g0031 a0002c0005t0100g0079 others(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 | a0001c0003t0098g0087 | 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 | a0001c0003t0101g0109 | 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 | a0001c0001t0043g0012 | 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 | a0001c0003t0083g0008 | 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 | a0001c0003t0051g0076 | 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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0003t0057g0104 | 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 | a0001c0002t0002g0151 | 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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0001c0002t0099g0135 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(95): 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 | a0001c0002t0092g0146 | 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:296929 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(86): 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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(86): 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 | a0001c0002t0087g0147 | 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 | a0001c0003t0051g0076 | 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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0001c0003t0101g0109 | 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 | a0001c0001t0019g0090 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0081g0061 | 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 | a0001c0001t0011g0091 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | 22 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(19): 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 | 33 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(30): 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 | 36 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(33): 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 | a0001c0002t0084g0156 | 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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0029g0059 others(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 | a0001c0003t0101g0109 | 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 | 30 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(27): 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 | TCCTG | T | 2 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(104): 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:297031 | A | T | 6 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0029g0059 others(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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0029g0059 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0015g0055 a0001c0001t0070g0152 a0001c0003t0059g0050 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0006g0038 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0003t0098g0087 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0002t0084g0156 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0002t0095g0139 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0001c0003t0083g0008 | 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 | a0001c0001t0013g0154 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0013g0010 a0001c0001t0029g0059 a0001c0001t0052g0072 others(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 | 20 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(17): 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 | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(108): 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 | a0001c0002t0088g0149 | 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 | 34 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(31): 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 | a0001c0002t0008g0138 | 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 | 20 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(17): 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 | a0001c0001t0011g0091 | 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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(86): 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 | a0001c0003t0101g0109 | 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 | a0001c0001t0022g0100 | 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 | a0001c0001t0022g0101 | 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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(86): 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 | a0001c0002t0084g0156 | 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 | a0001c0001t0044g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.734-1958T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297139 | |||||||
chrX:297161 | C | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0089g0096 | 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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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:297168 | T | C | 4 | a0001c0001t0015g0055 a0001c0001t0070g0152 a0001c0002t0084g0156 others(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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0002c0005t0026g0031 a0002c0005t0100g0079 a0002c0016t0026g0148 |
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 | a0001c0001t0015g0055 a0001c0001t0070g0152 a0001c0002t0084g0156 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0002c0016t0026g0148 | 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 | a0001c0001t0015g0055 a0001c0001t0070g0152 a0001c0002t0084g0156 others(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:297183 | G | A | 1 | a0001c0003t0083g0008 | 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 | a0001c0003t0051g0076 | 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 | a0001c0001t0013g0010 a0001c0001t0029g0059 a0001c0001t0052g0072 others(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 | 4 | a0001c0001t0001g0004 a0001c0001t0018g0102 a0001c0001t0076g0092 others(1): 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 | a0001c0002t0001g0137 | 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 | 20 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(17): 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 | 21 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(18): 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 | 26 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(23): 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 | a0001c0001t0013g0154 | 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 | a0001c0001t0005g0098 | 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 | a0001c0001t0015g0055 a0001c0001t0070g0152 a0001c0002t0084g0156 others(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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0001c0002t0091g0150 | 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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0054 others(68): 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 | a0001c0001t0009g0070 a0001c0001t0031g0014 a0001c0001t0032g0063 others(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 | a0001c0001t0002g0051 a0001c0001t0012g0134 a0001c0001t0021g0108 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0002c0005t0026g0031 a0002c0005t0100g0079 |
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 | a0001c0003t0083g0008 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0001c0003t0083g0008 others(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 | a0001c0001t0013g0010 | 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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0001g0054 a0001c0001t0061g0166 a0001c0001t0071g0168 others(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 | a0001c0001t0009g0077 a0001c0001t0040g0065 |
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 | a0001c0001t0020g0074 | 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 | a0002c0005t0026g0031 a0002c0005t0100g0079 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0016t0026g0148 others(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 | TGGGGATC others(141): Show |
T | 1 | a0001c0001t0015g0055 | 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 | a0001c0002t0084g0156 | 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 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1814G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297283 | |||||||
chrX:297286 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0053 others(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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0055g0007 |
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 | a0001c0001t0013g0010 a0001c0003t0015g0009 a0001c0003t0057g0104 others(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 | a0001c0001t0012g0133 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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:297315 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0013g0010 others(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 | a0001c0001t0013g0154 | 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 | a0001c0001t0013g0154 | 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 | a0001c0001t0013g0154 a0001c0001t0020g0074 a0001c0003t0101g0109 |
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 | a0001c0001t0044g0024 a0001c0001t0086g0088 a0001c0002t0002g0143 others(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:297325 | A | T | 2 | a0001c0001t0020g0074 a0001c0003t0101g0109 |
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 | a0002c0016t0026g0148 | 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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0001t0052g0072 | 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 | a0001c0001t0070g0152 a0001c0003t0059g0050 |
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 | a0001c0001t0001g0042 | 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 | a0001c0003t0015g0009 | 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 | a0001c0001t0001g0003 a0001c0001t0068g0103 a0001c0003t0083g0008 |
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 | a0001c0001t0081g0061 | 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 | a0001c0001t0001g0003 a0001c0001t0013g0154 a0001c0001t0020g0074 others(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 | a0001c0002t0085g0158 | 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 | a0001c0001t0001g0003 a0001c0001t0013g0154 a0001c0001t0020g0074 others(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 | a0002c0016t0026g0148 | 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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0001t0013g0154 a0001c0001t0022g0100 a0001c0001t0022g0101 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 a0001c0003t0055g0007 |
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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0020g0074 others(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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0020g0074 a0001c0001t0029g0059 a0001c0001t0052g0072 others(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 | a0001c0001t0013g0154 | 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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0002t0084g0156 a0001c0003t0051g0076 |
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 | a0001c0002t0103g0141 | 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 | a0001c0001t0068g0103 | 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 | a0001c0001t0029g0059 a0001c0003t0015g0009 |
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 | a0001c0002t0084g0156 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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:297482 | T | C | 1 | a0001c0003t0051g0076 | 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 | a0001c0003t0015g0009 | 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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0020g0074 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0003t0002g0165 | 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 | a0001c0001t0081g0061 | 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 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1583G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297514 | |||||||
chrX:297518 | C | A | 39 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0081g0061 | 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 | a0001c0001t0029g0059 a0001c0003t0055g0007 |
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 | a0001c0001t0005g0098 a0001c0001t0012g0134 a0001c0001t0021g0108 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0003t0051g0076 | 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 | a0001c0001t0005g0098 a0001c0001t0012g0134 a0001c0001t0021g0108 others(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 | a0001c0003t0098g0087 | 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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0002c0005t0100g0079 | 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 | a0001c0001t0052g0072 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-1498G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297599 | |||||||
chrX:297602 | C | A | 21 | a0001c0001t0013g0010 a0001c0001t0022g0100 a0001c0001t0022g0101 others(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 | a0001c0001t0029g0059 a0001c0003t0055g0007 |
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 | a0001c0003t0057g0104 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0013g0154 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0081g0061 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0003t0077g0164 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0003t0054g0085 a0001c0003t0056g0086 |
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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0010t0041g0167 | 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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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:297629 | T | TAGGACGT others(1267): Show |
1 | a0002c0016t0026g0148 | 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 | a0001c0010t0041g0167 | 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 | a0001c0003t0083g0008 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0005g0098 a0001c0001t0012g0133 a0001c0001t0022g0100 others(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 | a0001c0001t0013g0010 a0001c0003t0080g0157 |
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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0003t0051g0076 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0001c0003t0051g0076 others(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 | a0001c0001t0001g0054 a0001c0001t0005g0098 a0001c0001t0010g0083 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0054 a0001c0001t0005g0098 a0001c0001t0061g0166 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0005g0098 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0005g0098 others(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 | a0001c0001t0052g0072 | 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 | a0001c0001t0012g0133 a0001c0003t0101g0109 |
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 | a0001c0001t0070g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.734-1379C>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297718 | |||||||
chrX:297733 | G | A | 1 | a0001c0002t0084g0156 | 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 | a0001c0001t0029g0059 a0001c0003t0015g0009 a0001c0003t0055g0007 |
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 | a0001c0003t0083g0008 | 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 | a0001c0001t0001g0003 a0001c0001t0005g0098 a0001c0001t0012g0134 others(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 | a0001c0001t0013g0154 | 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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0005g0098 others(52): 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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0005g0098 others(52): 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 | a0001c0003t0051g0076 | 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 | a0001c0001t0001g0042 a0001c0001t0012g0134 a0001c0001t0020g0074 others(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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0029g0059 a0001c0001t0068g0103 a0001c0003t0006g0038 others(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 | a0001c0001t0029g0059 a0001c0001t0052g0072 a0001c0001t0068g0103 others(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 | a0001c0003t0101g0109 | 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 | a0001c0001t0052g0072 a0001c0001t0081g0061 |
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 | a0001c0001t0071g0168 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0005t0026g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0057 others(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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0005t0026g0031 others(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 | a0001c0001t0012g0134 a0001c0001t0021g0108 a0001c0001t0043g0012 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0002c0005t0100g0079 | 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 | a0001c0001t0001g0003 a0001c0001t0068g0103 a0001c0003t0080g0157 others(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 | a0001c0001t0001g0003 a0001c0001t0068g0103 a0001c0001t0081g0061 others(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 | a0001c0002t0004g0140 | 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 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0120 others(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 | a0001c0001t0081g0061 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0001c0010t0041g0167 others(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 | a0001c0002t0084g0156 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0068g0103 | 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 | a0001c0001t0068g0103 | 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 | a0001c0001t0009g0070 a0001c0001t0012g0134 a0001c0001t0021g0108 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 a0001c0003t0055g0007 |
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 | a0005c0015t0006g0078 | 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 | a0001c0003t0053g0105 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0163 a0001c0001t0005g0035 others(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 | a0001c0001t0029g0059 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | 26 | a0001c0001t0001g0004 a0001c0001t0003g0020 a0001c0001t0003g0022 others(23): 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 | a0001c0001t0068g0103 a0001c0002t0018g0111 |
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 | 20 | a0001c0001t0001g0004 a0001c0001t0010g0083 a0001c0001t0010g0089 others(17): 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 | a0001c0003t0083g0008 | 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 | a0001c0001t0052g0072 | 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 | a0001c0001t0001g0054 a0001c0001t0012g0133 a0001c0001t0012g0134 others(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 | a0001c0001t0001g0054 a0001c0001t0012g0133 a0001c0001t0012g0134 others(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 | 1 | a0001c0001t0001g0004 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0001c0001t0029g0059 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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:297928 | C | T | 2 | a0001c0003t0053g0105 a0001c0003t0083g0008 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0002t0004g0140 | 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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0002c0005t0026g0031 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0054 others(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 | a0001c0003t0057g0104 | 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 | a0001c0001t0012g0133 a0001c0001t0071g0168 |
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 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-1135A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 297962 | |||||||
chrX:297994 | A | C | 2 | a0001c0001t0001g0054 a0001c0003t0051g0076 |
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 | a0001c0003t0051g0076 | 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 | a0001c0001t0009g0070 a0001c0001t0020g0074 a0001c0001t0031g0014 others(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 | a0001c0001t0009g0070 a0001c0001t0020g0074 a0001c0001t0031g0014 others(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 | a0001c0001t0076g0092 a0001c0001t0081g0061 |
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 | a0001c0001t0001g0163 a0001c0001t0065g0029 a0001c0001t0075g0044 others(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 | a0002c0005t0100g0079 | 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 | a0001c0001t0052g0072 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0002c0016t0026g0148 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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:298040 | G | A | 1 | a0005c0015t0006g0078 | 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 | a0001c0001t0013g0154 | 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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(13): 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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0005c0015t0006g0078 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0005c0015t0006g0078 |
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 | a0001c0001t0001g0054 a0001c0001t0009g0068 |
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 | a0001c0001t0012g0133 a0001c0001t0052g0072 a0001c0003t0006g0038 others(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 | a0001c0002t0084g0156 | 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 | a0001c0001t0052g0072 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 a0001c0003t0055g0007 |
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:298057 | A | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | a0002c0005t0100g0079 | 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 | a0001c0003t0101g0109 | 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 | a0001c0010t0041g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1037A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298060 | |||||||
chrX:298091 | GACATTAT others(1): Show |
G | 2 | a0001c0001t0005g0035 a0001c0002t0023g0142 |
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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0057 a0001c0001t0005g0098 a0001c0001t0007g0128 others(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 | a0001c0001t0001g0057 a0001c0001t0005g0098 a0001c0001t0007g0128 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0042 |
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 | a0001c0001t0081g0061 a0001c0003t0053g0105 a0001c0003t0080g0157 |
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 | a0001c0001t0005g0035 a0001c0002t0023g0142 |
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 | 34 | a0001c0001t0001g0057 a0001c0001t0005g0098 a0001c0001t0007g0128 others(31): 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 | 41 | a0001c0001t0001g0057 a0001c0001t0005g0098 a0001c0001t0007g0128 others(38): 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 |
C | 1 | a0001c0001t0043g0012 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.734-990_734-893del others(98): Show |
PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298107 | |||||||
chrX:298107 | TCACATGG others(91): Show |
T | 1 | a0001c0002t0087g0147 | 1 | HG00738.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 | a0001c0003t0055g0007 | 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 | a0001c0001t0052g0072 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0001c0002t0084g0156 | 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 | a0001c0001t0068g0103 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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:298141 | A | ACATTATT others(139): Show |
1 | a0005c0015t0006g0078 | 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 | a0001c0001t0001g0057 a0001c0001t0005g0098 a0001c0001t0007g0128 others(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 | a0001c0003t0017g0048 | 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 | a0001c0003t0017g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.734-954A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298143 | |||||||
chrX:298148 | T | C | 3 | a0001c0001t0081g0061 a0001c0003t0080g0157 a0001c0010t0041g0167 |
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 | a0001c0001t0013g0154 | 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 | a0001c0003t0053g0105 | 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 | a0001c0001t0001g0057 a0001c0001t0007g0128 a0001c0001t0014g0028 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 |
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 | a0001c0001t0061g0166 | 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 | a0001c0001t0070g0152 | 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 | a0001c0001t0001g0057 a0001c0001t0007g0128 a0001c0001t0014g0028 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0068g0103 | 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 | a0001c0003t0057g0104 | 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 | a0001c0003t0055g0007 a0001c0010t0041g0167 |
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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0002c0016t0026g0148 others(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 | a0001c0001t0005g0035 a0001c0001t0015g0055 a0001c0001t0020g0074 others(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 | a0001c0001t0005g0098 | 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 | a0001c0001t0071g0168 | 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 | a0001c0001t0071g0168 | 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 | a0001c0001t0004g0025 a0001c0001t0004g0041 a0001c0001t0004g0110 others(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 | a0001c0001t0012g0134 a0001c0001t0021g0108 a0001c0003t0055g0007 others(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 | a0001c0001t0005g0035 a0001c0001t0015g0055 a0001c0002t0023g0142 others(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 | a0001c0001t0005g0035 a0001c0001t0015g0055 a0001c0002t0023g0142 others(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 | a0001c0003t0017g0048 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0001t0012g0134 a0001c0001t0013g0010 a0001c0001t0021g0108 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 a0001c0003t0055g0007 |
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:298217 | T | C | 4 | a0001c0001t0068g0103 a0001c0003t0027g0015 a0001c0003t0027g0016 others(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 | a0001c0001t0029g0059 a0001c0003t0015g0009 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 |
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 | a0001c0002t0045g0001 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.734-871G>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298226 | |||||||
chrX:298239 | A | ACATTATC others(42): Show |
1 | a0001c0001t0020g0074 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0061g0166 a0001c0001t0071g0168 |
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 | a0001c0001t0012g0134 a0001c0001t0020g0074 a0001c0001t0021g0108 others(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 | a0005c0015t0006g0078 | 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 | a0001c0003t0006g0039 a0001c0003t0006g0120 a0001c0003t0054g0085 |
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 | a0001c0010t0041g0167 | 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 | a0001c0002t0018g0111 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0052g0072 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-841A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298256 | |||||||
chrX:298271 | C | T | 2 | a0001c0002t0045g0001 a0001c0002t0046g0001 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0061g0166 a0001c0001t0071g0168 |
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 | a0001c0001t0002g0051 | 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 | a0001c0001t0013g0010 a0001c0001t0076g0092 a0001c0001t0081g0061 others(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 | a0001c0001t0013g0010 a0001c0001t0076g0092 a0001c0001t0081g0061 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | 1 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0084 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0005g0035 a0001c0001t0012g0134 a0001c0001t0015g0055 others(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 | a0001c0001t0052g0072 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.734-792A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298305 | |||||||
chrX:298320 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0009g0070 others(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 | 70 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0053 others(67): 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 | a0001c0003t0015g0009 | 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 | a0001c0003t0006g0038 a0001c0003t0056g0086 |
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 | a0001c0003t0098g0087 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0027g0015 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0027g0015 others(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 | a0001c0001t0013g0010 a0001c0001t0076g0092 a0001c0002t0018g0111 |
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 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(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 | a0001c0001t0029g0059 | 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 | a0001c0003t0055g0007 | 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 | a0002c0005t0100g0079 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0009g0070 others(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 | a0001c0001t0068g0103 | 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 | a0001c0003t0057g0104 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0009g0070 others(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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0012g0133 a0001c0001t0029g0059 a0001c0003t0015g0009 others(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 | 71 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(68): 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 | 74 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(71): 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 | a0002c0005t0026g0031 | 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 | a0001c0003t0055g0007 a0001c0003t0101g0109 a0002c0005t0100g0079 |
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 | a0001c0001t0001g0042 a0001c0001t0009g0070 a0001c0001t0031g0014 others(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 | a0001c0001t0076g0092 | 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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | a0001c0001t0052g0072 | 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 | a0001c0003t0051g0076 | 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 | a0001c0003t0055g0007 | 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 | a0001c0001t0012g0133 a0001c0001t0029g0059 a0001c0001t0076g0092 others(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 | a0001c0002t0084g0156 | 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 | a0001c0002t0084g0156 | 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 | a0001c0001t0012g0133 a0001c0001t0029g0059 a0001c0003t0006g0038 others(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 | a0001c0001t0013g0154 | 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 | a0001c0001t0001g0042 a0001c0001t0009g0070 a0001c0001t0013g0010 others(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 | a0001c0001t0001g0042 a0001c0001t0009g0070 a0001c0001t0013g0010 others(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 | a0001c0003t0101g0109 | 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:298462 | T | C | 1 | a0001c0002t0018g0111 | 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 | a0001c0001t0001g0003 a0002c0016t0026g0148 |
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 | 32 | a0001c0001t0004g0025 a0001c0001t0010g0083 a0001c0001t0010g0089 others(29): 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 | 19 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(16): 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 | 19 | a0001c0001t0010g0083 a0001c0001t0010g0089 a0001c0001t0010g0097 others(16): 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 | a0001c0001t0029g0059 a0001c0003t0006g0038 a0001c0003t0006g0039 others(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 | a0001c0003t0053g0105 | 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 | a0001c0001t0001g0042 a0001c0001t0081g0061 |
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 | a0001c0001t0004g0025 a0001c0001t0009g0070 a0001c0001t0013g0010 others(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 | a0001c0003t0051g0076 | 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 | a0001c0001t0052g0072 | 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 | a0001c0001t0004g0025 a0001c0001t0009g0070 a0001c0001t0013g0010 others(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 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-596A>T | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298501 | |||||||
chrX:298516 | C | T | 62 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(59): 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 | a0001c0003t0053g0105 a0001c0003t0055g0007 |
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:298540 | T | TCTGTCTA others(42): Show |
1 | a0001c0001t0020g0074 | 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 | a0001c0003t0055g0007 | 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 | a0001c0001t0076g0092 | 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:298547 | A | C | 7 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0022g0100 others(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 | a0001c0001t0013g0010 a0001c0001t0013g0154 a0001c0001t0022g0100 others(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 | a0001c0003t0027g0015 a0001c0003t0027g0016 a0006c0011t0102g0017 |
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 | 56 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(53): 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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0002c0005t0026g0031 others(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 | a0001c0001t0064g0036 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.734-525A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298572 | |||||||
chrX:298581 | G | A | 1 | a0001c0001t0089g0096 | 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 | 40 | a0001c0001t0001g0003 a0001c0001t0009g0070 a0001c0001t0010g0083 others(37): 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0020g0074 a0001c0003t0055g0007 |
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 | a0001c0002t0018g0111 | 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 | a0001c0001t0001g0003 a0001c0001t0022g0100 a0001c0001t0022g0101 others(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 | a0001c0001t0001g0003 a0001c0001t0022g0100 a0001c0001t0022g0101 others(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 | 57 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(54): 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 | a0001c0001t0013g0010 | 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 | a0001c0002t0088g0149 | 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 | 110 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0054 others(107): 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0001t0029g0059 others(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 | a0001c0003t0101g0109 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.734-482G>A | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298615 | |||||||
chrX:298631 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0013g0010 |
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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0001c0001t0022g0100 others(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 | a0001c0003t0051g0076 | 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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0001c0001t0022g0100 others(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:298652 | G | T | 1 | a0001c0003t0101g0109 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0083g0008 |
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 | a0001c0001t0013g0154 | 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 | a0002c0016t0026g0148 | 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 | a0001c0001t0022g0100 a0001c0001t0022g0101 a0001c0003t0055g0007 others(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 | a0001c0002t0084g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.734-415A>G | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298682 | |||||||
chrX:298687 | T | C | 1 | a0001c0003t0057g0104 | 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 | 79 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(76): 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 | a0001c0002t0084g0156 | 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 | a0001c0001t0001g0003 a0001c0001t0013g0010 |
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 | a0001c0001t0001g0003 a0001c0001t0013g0010 |
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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0001c0001t0020g0074 others(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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0001c0001t0022g0100 others(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 | a0001c0001t0013g0154 | 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 | a0001c0001t0020g0074 | 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 | a0001c0001t0001g0003 a0001c0001t0013g0010 a0001c0001t0013g0154 others(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 | 25 | a0001c0001t0009g0070 a0001c0001t0010g0083 a0001c0001t0010g0089 others(22): 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 | 25 | a0001c0001t0009g0070 a0001c0001t0010g0083 a0001c0001t0010g0089 others(22): 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 | a0001c0003t0101g0109 | 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 | a0006c0011t0102g0017 | 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 | a0001c0003t0027g0015 | 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 | a0001c0003t0027g0016 | 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 | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(93): 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:298778 | A | C | 1 | a0001c0003t0051g0076 | 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 | 28 | a0001c0001t0009g0070 a0001c0001t0010g0083 a0001c0001t0010g0089 others(25): 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 | a0001c0003t0101g0109 | 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:298827 | C | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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:298859 | T | C | 3 | a0001c0001t0029g0059 a0001c0001t0052g0072 a0001c0003t0015g0009 |
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 | a0001c0001t0029g0059 a0001c0001t0052g0072 a0001c0003t0015g0009 |
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 | a0001c0003t0057g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.734-168T>C | PLCXD1 | ENSG00000182378.15 | transcript | ENST00000381657.8 | protein_coding | 6/6 | chrX | 298929 |