geneid | 84552 |
---|---|
ensemblid | ENSG00000178184.16 |
hgncid | 16076 |
symbol | PARD6G |
name | par-6 family cell polarity regulator gamma |
refseq_nuc | NM_032510.4 |
refseq_prot | NP_115899.1 |
ensembl_nuc | ENST00000353265.8 |
ensembl_prot | ENSP00000343144.3 |
mane_status | MANE Select |
chr | chr18 |
start | 80157232 |
end | 80247514 |
strand | - |
ver | v1.2 |
region | chr18:80157232-80247514 |
region5000 | chr18:80152232-80252514 |
regionname0 | PARD6G_chr18_80157232_80247514 |
regionname5000 | PARD6G_chr18_80152232_80252514 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 376 | 380 | 91 | 72 | 165 | 12 | 38 | 136 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0002 | 0/0 | 376 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0003 | 0/0 | 376 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1131 | 262 | 70 | 56 | 97 | 9 | 28 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0002 | 0/0 | 1131 | 111 | 19 | 15 | 66 | 3 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0003 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0004 | 0/0 | 1131 | 2 | 0 | 0 | 0 | 0 | 2 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0005 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0006 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0007 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0008 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
c0009 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2709 | 82 | 1 | 16 | 54 | 3 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0002 | 1/1 | 2706 | 76 | 0 | 13 | 52 | 1 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0003 | 0/0 | 2706 | 56 | 30 | 9 | 12 | 2 | 3 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0004 | 0/0 | 2705 | 44 | 10 | 8 | 10 | 3 | 13 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0005 | 0/0 | 2709 | 43 | 1 | 11 | 23 | 3 | 5 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0006 | 0/0 | 2709 | 19 | 11 | 2 | 6 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0007 | 0/0 | 2706 | 13 | 10 | 3 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0008 | 0/0 | 2706 | 7 | 5 | 1 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0009 | 0/0 | 2709 | 6 | 0 | 0 | 6 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0010 | 0/0 | 2706 | 4 | 3 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0011 | 0/0 | 2721 | 4 | 4 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0012 | 0/0 | 2706 | 3 | 2 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0013 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0014 | 0/0 | 2706 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0015 | 0/0 | 2709 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0016 | 0/0 | 2706 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0017 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0018 | 0/0 | 2706 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0019 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0020 | 0/0 | 2705 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0021 | 0/0 | 2705 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0022 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0023 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0024 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0025 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0026 | 0/0 | 2710 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0027 | 0/0 | 2705 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0028 | 0/0 | 2709 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0029 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0030 | 0/0 | 2709 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0031 | 0/0 | 2706 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0032 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
t0033 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1131 | 262 | 70 | 56 | 97 | 9 | 28 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002 | 0/0 | 1131 | 111 | 19 | 15 | 66 | 3 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0003 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0004 | 0/0 | 1131 | 2 | 0 | 0 | 0 | 0 | 2 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0005 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0007 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0008 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0002c0006 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0003c0009 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3839 | 9 | 0 | 5 | 4 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0002 | 1/1 | 3836 | 70 | 0 | 13 | 46 | 1 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0003 | 0/0 | 3836 | 55 | 29 | 9 | 12 | 2 | 3 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0004 | 0/0 | 3835 | 41 | 10 | 7 | 10 | 3 | 11 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0005 | 0/0 | 3839 | 42 | 1 | 11 | 22 | 3 | 5 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0006 | 0/0 | 3839 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0007 | 0/0 | 3836 | 13 | 10 | 3 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0008 | 0/0 | 3836 | 5 | 3 | 1 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0010 | 0/0 | 3836 | 4 | 3 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0012 | 0/0 | 3836 | 3 | 2 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0014 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0016 | 0/0 | 3836 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0017 | 0/0 | 3839 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0018 | 0/0 | 3836 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0019 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0020 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0021 | 0/0 | 3835 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0022 | 0/0 | 3839 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0023 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0024 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0025 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0026 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0027 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0030 | 0/0 | 3839 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0031 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0032 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0001t0033 | 0/0 | 3794 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0001 | 0/0 | 3839 | 72 | 1 | 11 | 49 | 3 | 8 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0002 | 0/0 | 3836 | 5 | 0 | 0 | 5 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0003 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0004 | 0/0 | 3835 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0006 | 0/0 | 3839 | 17 | 11 | 0 | 6 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0009 | 0/0 | 3839 | 6 | 0 | 0 | 6 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0011 | 0/0 | 3851 | 4 | 4 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0013 | 0/0 | 3851 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0015 | 0/0 | 3839 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0002t0029 | 0/0 | 3839 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0003t0008 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0004t0004 | 0/0 | 3835 | 2 | 0 | 0 | 0 | 0 | 2 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0005t0001 | 0/0 | 3839 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0007t0002 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0001c0008t0006 | 0/0 | 3839 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0002c0006t0028 | 0/0 | 3839 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
a0003c0009t0005 | 0/0 | 3839 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | copy fasta | chr18 | 80152232 | 80252514 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0010g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0012g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0016g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0018g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0019g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0020g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0021g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0022g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0026g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0027g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0030g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0031g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0032g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0001t0033g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0009g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0011g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0011g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0011g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0015g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0015g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0002t0029g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0003t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0003t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0004t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0004t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0007t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0001c0008t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0002c0006t0028g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
a0003c0009t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0323 | EUR | GBR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0259 | EUR | GBR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0239 | EUR | GBR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | FIN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0204 | EUR | FIN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00438 | hp1 | a0001 | c0002 | t0009 | g0215 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00642 | hp1 | a0001 | c0001 | t0021 | g0220 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00642 | hp2 | a0001 | c0002 | t0015 | g0186 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0361 | EAS | CHS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00738 | hp1 | a0001 | c0002 | t0015 | g0185 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0062 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0244 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0251 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0103 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0096 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0095 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0087 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01255 | hp1 | a0001 | c0008 | t0006 | g0260 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0258 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01256 | hp1 | a0001 | c0002 | t0029 | g0255 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0234 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0222 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0304 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0196 | EUR | IBS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0248 | EUR | IBS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0061 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0209 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01891 | hp1 | a0001 | c0001 | t0010 | g0089 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01891 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0355 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01981 | hp1 | a0001 | c0002 | t0004 | g0219 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02132 | hp1 | a0003 | c0009 | t0005 | g0049 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02257 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02258 | hp1 | a0001 | c0002 | t0013 | g0011 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02273 | hp1 | a0001 | c0001 | t0030 | g0266 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02280 | hp2 | a0001 | c0001 | t0019 | g0017 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0170 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0357 | AMR | PEL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0201 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0030 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0292 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0367 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0314 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02809 | hp1 | a0001 | c0003 | t0008 | g0082 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02886 | hp1 | a0001 | c0001 | t0032 | g0067 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0086 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02965 | hp1 | a0001 | c0001 | t0026 | g0084 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0180 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0226 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03041 | hp1 | a0001 | c0002 | t0006 | g0078 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0279 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0366 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03130 | hp1 | a0001 | c0001 | t0023 | g0228 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0350 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0091 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0018 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03225 | hp2 | a0001 | c0002 | t0006 | g0014 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03453 | hp2 | a0002 | c0006 | t0028 | g0081 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0231 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03492 | hp1 | a0001 | c0004 | t0004 | g0192 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0365 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | ESN | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0316 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03579 | hp1 | a0001 | c0002 | t0011 | g0371 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0249 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0245 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0320 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0363 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03704 | hp1 | a0001 | c0001 | t0018 | g0154 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03704 | hp2 | a0001 | c0004 | t0004 | g0190 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0195 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0331 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0205 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0328 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0285 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0207 | SAS | STU | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18522 | hp1 | a0001 | c0001 | t0024 | g0088 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | CHB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | CHB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18906 | hp2 | a0001 | c0002 | t0006 | g0351 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0338 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0345 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18963 | hp1 | a0001 | c0002 | t0006 | g0274 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18966 | hp1 | a0001 | c0002 | t0006 | g0270 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18966 | hp2 | a0001 | c0007 | t0002 | g0126 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18973 | hp1 | a0001 | c0002 | t0009 | g0321 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0341 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18977 | hp2 | a0001 | c0002 | t0006 | g0272 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18982 | hp1 | a0001 | c0002 | t0006 | g0269 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18984 | hp2 | a0001 | c0002 | t0006 | g0273 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18987 | hp1 | a0001 | c0002 | t0009 | g0319 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18990 | hp1 | a0001 | c0002 | t0009 | g0322 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18991 | hp2 | a0001 | c0002 | t0006 | g0271 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18994 | hp2 | a0001 | c0002 | t0009 | g0317 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0343 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19006 | hp1 | a0001 | c0002 | t0009 | g0312 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0344 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0339 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0313 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19043 | hp1 | a0001 | c0002 | t0011 | g0370 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19043 | hp2 | a0001 | c0003 | t0008 | g0083 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19054 | hp1 | a0001 | c0001 | t0031 | g0039 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0346 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19055 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0342 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19089 | hp2 | a0001 | c0005 | t0001 | g0309 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19091 | hp2 | a0001 | c0001 | t0033 | g0369 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | YRI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0315 | AFR | ASW | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | ASW | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0236 | EUR | TSI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0051 | EUR | TSI | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | GIH | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | GIH | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | CLM | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02109 | hp1 | a0001 | c0001 | t0027 | g0368 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0278 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0230 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | MSL | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | USA | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
HG06807 | hp2 | a0001 | c0002 | t0013 | g0012 | AFR | USA | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | USA | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | USA | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0188 | REF | REF | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0128 | REF | REF | PARD6G_chr18_80152232_80252514 | PARD6G | chr18 | 80152232 | 80252514 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:80159841
|
G | C | 1 | a0002 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1061C>G | p.Ala354Gly | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1227/3836 | 1061/1131 | 354/376 | chr18 | 80159841 | ||
chr18:80160415
|
G | A | 1 | a0003 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.487C>T | p.Arg163Trp | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 653/3836 | 487/1131 | 163/376 | chr18 | 80160415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:80159900
|
C | A | 1 | a0001c0008 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1002G>T | p.Arg334Arg | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1168/3836 | 1002/1131 | 334/376 | chr18 | 80159900 | ||
chr18:80160173
|
G | A | 1 | a0001c0004 | 2 | HG03492.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.729C>T | p.Leu243Leu | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 895/3836 | 729/1131 | 243/376 | chr18 | 80160173 | ||
chr18:80160338
|
C | T | 3 | a0001c0002a0001c0005a0001c0008 | 113 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
synonymous_variant | LOW | c.564G>A | p.Glu188Glu | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 730/3836 | 564/1131 | 188/376 | chr18 | 80160338 | ||
chr18:80160458
|
A | G | 1 | a0001c0007 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.444T>C | p.Asp148Asp | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 610/3836 | 444/1131 | 148/376 | chr18 | 80160458 | ||
chr18:80202756
|
C | T | 2 | a0001c0003a0002c0006 | 3 | HG02809.hp1 HG03453.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.249G>A | p.Ala83Ala | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/3 | 415/3836 | 249/1131 | 83/376 | chr18 | 80202756 | ||
chr18:80202828
|
A | G | 1 | a0001c0005 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.177T>C | p.Asp59Asp | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/3 | 343/3836 | 177/1131 | 59/376 | chr18 | 80202828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:80157415
|
C | T | 1 | a0001c0002t0029 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2356G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2356 | chr18 | 80157415 | |||||
chr18:80157487
|
A | G | 1 | a0001c0001t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2284T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2284 | chr18 | 80157487 | |||||
chr18:80157500
|
C | T | 11 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(8): Show | 76 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2271G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2271 | chr18 | 80157500 | |||||
chr18:80157550
|
A | AACTT | 18 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(15): Show | 164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2217_*2220dupAAGT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2220 | chr18 | 80157550 | |||||
chr18:80157551
|
A | T | 1 | a0001c0001t0024 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2220 | chr18 | 80157551 | |||||
chr18:80157678
|
T | A | 1 | a0001c0001t0031 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2093 | chr18 | 80157678 | |||||
chr18:80157769
|
A | C | 1 | a0001c0002t0029 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2002T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 2002 | chr18 | 80157769 | |||||
chr18:80157815
|
A | C | 36 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1956T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1956 | chr18 | 80157815 | |||||
chr18:80158023
|
T | C | 6 | a0001c0001t0004a0001c0001t0020a0001c0001t0021others(3): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1748A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1748 | chr18 | 80158023 | |||||
chr18:80158132
|
T | C | 6 | a0001c0001t0004a0001c0001t0020a0001c0001t0021others(3): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1639A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1639 | chr18 | 80158132 | |||||
chr18:80158163
|
A | G | 2 | a0001c0002t0015a0001c0002t0029 | 3 | HG00642.hp2 HG00738.hp1 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1608T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1608 | chr18 | 80158163 | |||||
chr18:80158418
|
A | C | 1 | a0001c0001t0027 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1353T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1353 | chr18 | 80158418 | |||||
chr18:80158499
|
T | C | 2 | a0001c0001t0005a0003c0009t0005 | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1272A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1272 | chr18 | 80158499 | |||||
chr18:80158531
|
G | C | 12 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(9): Show | 77 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1240C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1240 | chr18 | 80158531 | |||||
chr18:80158602
|
T | C | 7 | a0001c0001t0001a0001c0001t0030a0001c0002t0001others(4): Show | 92 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1169 | chr18 | 80158602 | |||||
chr18:80158615
|
G | C | 1 | a0001c0002t0009 | 6 | HG00438.hp1 NA18973.hp1 NA18987.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1156 | chr18 | 80158615 | |||||
chr18:80158682
|
T | C | 6 | a0001c0001t0003a0001c0001t0012a0001c0001t0031others(3): Show | 62 | HG00323.hp1 HG01069.hp2 HG01192.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1089A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 1089 | chr18 | 80158682 | |||||
chr18:80158808
|
T | C | 6 | a0001c0001t0004a0001c0001t0020a0001c0001t0021others(3): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*963A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 963 | chr18 | 80158808 | |||||
chr18:80158835
|
T | C | 1 | a0001c0001t0012 | 3 | HG01069.hp2 HG01884.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*936A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 936 | chr18 | 80158835 | |||||
chr18:80158991
|
AT | A | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(20): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*779delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 779 | chr18 | 80158991 | |||||
chr18:80159003
|
T | C | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 768 | chr18 | 80159003 | |||||
chr18:80159082
|
G | A | 1 | a0001c0001t0030 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 689 | chr18 | 80159082 | |||||
chr18:80159179
|
A | G | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(14): Show | 123 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*592T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 592 | chr18 | 80159179 | |||||
chr18:80159189
|
C | A | 11 | a0001c0001t0001a0001c0001t0006a0001c0001t0030others(8): Show | 115 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 582 | chr18 | 80159189 | |||||
chr18:80159200
|
T | G | 1 | a0001c0001t0021 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 571 | chr18 | 80159200 | |||||
chr18:80159381
|
T | C | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*390A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 390 | chr18 | 80159381 | |||||
chr18:80159406
|
A | G | 1 | a0001c0001t0022 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 365 | chr18 | 80159406 | |||||
chr18:80159525
|
G | C | 1 | a0001c0001t0010 | 4 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*246C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 246 | chr18 | 80159525 | |||||
chr18:80159567
|
C | G | 7 | a0001c0001t0004a0001c0001t0018a0001c0001t0019others(4): Show | 48 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 204 | chr18 | 80159567 | |||||
chr18:80159596
|
G | A | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(6): Show | 73 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 175 | chr18 | 80159596 | |||||
chr18:80159751
|
T | G | 1 | a0001c0001t0032 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 20 | chr18 | 80159751 | |||||
chr18:80159755
|
G | A | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 16 | chr18 | 80159755 | |||||
chr18:80159764
|
C | T | 1 | a0001c0001t0017 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 3/3 | 7 | chr18 | 80159764 | |||||
chr18:80247370
|
CGCCGTCG others(35): Show |
C | 1 | a0001c0001t0033 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64_-23delCCGGGAGT others(34): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/3 | 23 | chr18 | 80247370 | |||||
chr18:80247426
|
A | AGGCCCCG others(5): Show |
2 | a0001c0002t0011a0001c0002t0013 | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-79dupGGGGCCGG others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/3 | 79 | chr18 | 80247426 | |||||
chr18:80247464
|
G | A | 1 | a0001c0002t0011 | 4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-116C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/3 | chr18 | 80247464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:80160663
|
G | A | 1 | a0001c0001t0008g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.296-57C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160663 | ||||||
chr18:80160667
|
G | A | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-61C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160667 | ||||||
chr18:80160739
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-133G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160739 | ||||||
chr18:80160744
|
GGCTGA | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0175a0001c0001t0004g0176others(41): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-143_296-139del others(5): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160744 | ||||||
chr18:80160754
|
A | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0175a0001c0001t0004g0176others(41): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-148T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160754 | ||||||
chr18:80160901
|
G | A | 4 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0003t0008g0082others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-295C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80160901 | ||||||
chr18:80161200
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.296-594C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80161200 | ||||||
chr18:80161640
|
C | T | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.296-1034G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80161640 | ||||||
chr18:80161688
|
T | A | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-1082A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80161688 | ||||||
chr18:80161748
|
T | A | 1 | a0001c0001t0004g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.296-1142A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80161748 | ||||||
chr18:80161929
|
G | T | 1 | a0001c0001t0003g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.296-1323C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80161929 | ||||||
chr18:80162010
|
C | G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-1404G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162010 | ||||||
chr18:80162226
|
A | G | 1 | a0001c0001t0026g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.296-1620T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162226 | ||||||
chr18:80162269
|
T | C | 5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-1663A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162269 | ||||||
chr18:80162307
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-1701C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162307 | ||||||
chr18:80162533
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.296-1927G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162533 | ||||||
chr18:80162601
|
C | T | 7 | a0001c0002t0006g0350a0001c0002t0006g0351a0001c0002t0011g0010others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-1995G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162601 | ||||||
chr18:80162809
|
C | T | 14 | a0001c0001t0007g0021a0001c0001t0007g0103a0001c0001t0007g0104others(11): Show | 14 | HG01074.hp1 HG01106.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.296-2203G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162809 | ||||||
chr18:80162840
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-2234G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162840 | ||||||
chr18:80162895
|
T | C | 1 | a0001c0001t0002g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.296-2289A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80162895 | ||||||
chr18:80163040
|
C | T | 4 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(1): Show | 4 | HG02056.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2434G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163040 | ||||||
chr18:80163351
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.296-2745G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163351 | ||||||
chr18:80163366
|
C | T | 2 | a0001c0001t0003g0024a0001c0001t0003g0046 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.296-2760G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163366 | ||||||
chr18:80163393
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.296-2787C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163393 | ||||||
chr18:80163448
|
CAG | C | 120 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(117): Show | 123 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.296-2844_296-2843d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163448 | ||||||
chr18:80163523
|
G | A | 14 | a0001c0001t0002g0127a0001c0001t0002g0132a0001c0001t0002g0137others(11): Show | 14 | HG00423.hp2 HG00597.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-2917C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163523 | ||||||
chr18:80163600
|
T | C | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-2994A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80163600 | ||||||
chr18:80164008
|
G | C | 52 | a0001c0001t0002g0107a0001c0001t0003g0044a0001c0001t0003g0182others(49): Show | 54 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.296-3402C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164008 | ||||||
chr18:80164071
|
A | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(110): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.296-3465T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164071 | ||||||
chr18:80164122
|
C | A | 1 | a0001c0001t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.296-3516G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164122 | ||||||
chr18:80164185
|
C | A | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-3579G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164185 | ||||||
chr18:80164255
|
G | A | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-3649C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164255 | ||||||
chr18:80164351
|
C | T | 1 | a0001c0001t0005g0343 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.296-3745G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164351 | ||||||
chr18:80164352
|
T | C | 1 | a0001c0001t0005g0343 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.296-3746A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164352 | ||||||
chr18:80164361
|
C | T | 66 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(63): Show | 67 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.296-3755G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164361 | ||||||
chr18:80164461
|
C | T | 1 | a0001c0002t0006g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.296-3855G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164461 | ||||||
chr18:80164486
|
C | A | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.296-3880G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164486 | ||||||
chr18:80164499
|
T | C | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-3893A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164499 | ||||||
chr18:80164702
|
C | A | 274 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(271): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.296-4096G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164702 | ||||||
chr18:80164881
|
A | C | 1 | a0001c0001t0002g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.296-4275T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80164881 | ||||||
chr18:80165030
|
A | C | 45 | a0001c0001t0004g0001a0001c0001t0004g0175a0001c0001t0004g0176others(42): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.296-4424T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165030 | ||||||
chr18:80165030
|
A | G | 155 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(152): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.296-4424T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165030 | ||||||
chr18:80165156
|
C | G | 5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-4550G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165156 | ||||||
chr18:80165170
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-4564C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165170 | ||||||
chr18:80165401
|
C | G | 2 | a0001c0001t0004g0194a0001c0001t0004g0214 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.296-4795G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165401 | ||||||
chr18:80165469
|
CAT | C | 14 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0068others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.296-4865_296-4864d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165469 | ||||||
chr18:80165496
|
A | C | 273 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(270): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.296-4890T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165496 | ||||||
chr18:80165539
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.296-4933G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165539 | ||||||
chr18:80165561
|
T | TTAAAG | 274 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(271): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.296-4960_296-4956d others(7): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165561 | ||||||
chr18:80165688
|
C | T | 2 | a0001c0002t0006g0078a0001c0002t0006g0279 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-5082G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165688 | ||||||
chr18:80165689
|
G | A | 2 | a0001c0001t0004g0175a0001c0001t0004g0176 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.296-5083C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165689 | ||||||
chr18:80165699
|
T | C | 1 | a0001c0002t0001g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.296-5093A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165699 | ||||||
chr18:80165702
|
C | G | 1 | a0001c0002t0001g0290 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.296-5096G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165702 | ||||||
chr18:80165736
|
G | GA | 43 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-5131dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80165736 | ||||||
chr18:80166015
|
C | T | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.296-5409G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166015 | ||||||
chr18:80166075
|
T | C | 155 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(152): Show | 161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.296-5469A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166075 | ||||||
chr18:80166100
|
C | T | 1 | a0001c0002t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.296-5494G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166100 | ||||||
chr18:80166147
|
A | G | 1 | a0001c0002t0001g0311 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.296-5541T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166147 | ||||||
chr18:80166160
|
T | C | 44 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(41): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-5554A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166160 | ||||||
chr18:80166206
|
G | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-5600C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166206 | ||||||
chr18:80166278
|
G | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-5672C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166278 | ||||||
chr18:80166388
|
T | C | 44 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(41): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-5782A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166388 | ||||||
chr18:80166496
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-5890C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166496 | ||||||
chr18:80166650
|
C | T | 1 | a0001c0001t0023g0228 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.296-6044G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166650 | ||||||
chr18:80166726
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.296-6120A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166726 | ||||||
chr18:80166975
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-6369G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80166975 | ||||||
chr18:80167115
|
G | A | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-6509C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167115 | ||||||
chr18:80167181
|
G | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-6575C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167181 | ||||||
chr18:80167207
|
GTGGGCAG others(33): Show |
G | 1 | a0001c0001t0005g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.296-6641_296-6602d others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167207 | ||||||
chr18:80167220
|
T | C | 271 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.296-6614A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167220 | ||||||
chr18:80167268
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-6662G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167268 | ||||||
chr18:80167272
|
TTGCAGGA others(73): Show |
T | 4 | a0001c0001t0002g0100a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG00140.hp1 HG00738.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-6746_296-6667d others(82): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167272 | ||||||
chr18:80167391
|
G | A | 1 | a0002c0006t0028g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-6785C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167391 | ||||||
chr18:80167542
|
G | A | 1 | a0001c0001t0007g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.296-6936C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167542 | ||||||
chr18:80167710
|
G | A | 23 | a0001c0001t0003g0002a0001c0001t0003g0026a0001c0001t0003g0027others(20): Show | 24 | HG00323.hp1 HG01192.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-7104C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167710 | ||||||
chr18:80167718
|
G | T | 1 | a0001c0001t0003g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.296-7112C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167718 | ||||||
chr18:80167744
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.296-7138G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80167744 | ||||||
chr18:80168072
|
G | A | 1 | a0001c0002t0006g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296-7466C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168072 | ||||||
chr18:80168311
|
A | C | 1 | a0001c0001t0002g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.296-7705T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168311 | ||||||
chr18:80168314
|
C | A | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.296-7708G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168314 | ||||||
chr18:80168455
|
T | G | 73 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-7849A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168455 | ||||||
chr18:80168538
|
T | C | 1 | a0001c0007t0002g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.296-7932A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168538 | ||||||
chr18:80168573
|
T | TTG | 61 | a0001c0001t0001g0295a0001c0001t0002g0003a0001c0001t0002g0107others(58): Show | 62 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.296-7969_296-7968d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
T | TTGTG | 70 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0293others(67): Show | 75 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.296-7971_296-7968d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
T | TTGTGTG | 17 | a0001c0001t0001g0287a0001c0001t0001g0329a0001c0001t0004g0225others(14): Show | 17 | HG01109.hp1 HG02056.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-7973_296-7968d others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
T | TTGTGTGT others(1): Show |
3 | a0001c0002t0001g0292a0001c0002t0001g0358a0001c0002t0001g0359 | 3 | HG02698.hp1 NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.296-7975_296-7968d others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.296-7979_296-7968d others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
TTG | T | 61 | a0001c0001t0004g0175a0001c0001t0004g0176a0001c0001t0004g0216others(58): Show | 62 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.296-7969_296-7968d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
TTGTGTGT others(1): Show |
T | 2 | a0001c0002t0001g0006a0001c0002t0001g0364 | 3 | NA18979.hp1 NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.296-7975_296-7968d others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168573
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-7977_296-7968d others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168573 | ||||||
chr18:80168607
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.296-8001C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168607 | ||||||
chr18:80168609
|
A | G | 1 | a0001c0002t0001g0264 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.296-8003T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168609 | ||||||
chr18:80168624
|
CT | C | 8 | a0001c0001t0005g0332a0001c0001t0005g0333a0001c0001t0005g0337others(5): Show | 8 | HG00621.hp2 NA18943.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-8019delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168624 | ||||||
chr18:80168686
|
C | T | 1 | a0001c0002t0001g0320 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.296-8080G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168686 | ||||||
chr18:80168900
|
G | A | 6 | a0001c0001t0003g0028a0001c0001t0003g0036a0001c0001t0003g0063others(3): Show | 6 | HG01952.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-8294C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168900 | ||||||
chr18:80168912
|
T | TACAAATA others(2): Show |
73 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-8315_296-8307d others(11): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168912 | ||||||
chr18:80168979
|
G | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-8373C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80168979 | ||||||
chr18:80169003
|
G | A | 1 | a0001c0001t0007g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.296-8397C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169003 | ||||||
chr18:80169038
|
G | A | 1 | a0001c0001t0002g0135 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.296-8432C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169038 | ||||||
chr18:80169089
|
G | A | 1 | a0001c0001t0004g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.296-8483C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169089 | ||||||
chr18:80169117
|
A | T | 1 | a0001c0001t0007g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.296-8511T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169117 | ||||||
chr18:80169145
|
A | G | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.296-8539T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169145 | ||||||
chr18:80169229
|
G | A | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.296-8623C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169229 | ||||||
chr18:80169414
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.296-8808C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169414 | ||||||
chr18:80169449
|
C | A | 1 | a0001c0001t0004g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.296-8843G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169449 | ||||||
chr18:80169689
|
T | C | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-9083A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169689 | ||||||
chr18:80169725
|
T | C | 156 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(153): Show | 162 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.296-9119A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169725 | ||||||
chr18:80169757
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.296-9151G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169757 | ||||||
chr18:80169850
|
G | A | 1 | a0001c0002t0001g0354 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.296-9244C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169850 | ||||||
chr18:80169938
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-9332G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169938 | ||||||
chr18:80169983
|
A | G | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.296-9377T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169983 | ||||||
chr18:80169993
|
G | A | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-9387C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80169993 | ||||||
chr18:80170119
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.296-9513C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170119 | ||||||
chr18:80170442
|
A | C | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-9836T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170442 | ||||||
chr18:80170462
|
G | C | 44 | a0001c0001t0003g0182a0001c0001t0004g0001a0001c0001t0004g0187others(41): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-9856C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170462 | ||||||
chr18:80170475
|
C | T | 3 | a0001c0002t0006g0014a0001c0002t0006g0078a0001c0002t0006g0279 | 3 | HG03041.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.296-9869G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170475 | ||||||
chr18:80170514
|
C | T | 4 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(1): Show | 4 | HG02056.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-9908G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170514 | ||||||
chr18:80170563
|
G | A | 1 | a0001c0002t0001g0307 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.296-9957C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170563 | ||||||
chr18:80170620
|
C | T | 3 | a0001c0001t0004g0206a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG00733.hp1 HG01433.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.296-10014G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170620 | ||||||
chr18:80170702
|
T | C | 3 | a0001c0001t0003g0177a0001c0001t0003g0179a0001c0001t0033g0369 | 3 | NA18941.hp2 NA19004.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.296-10096A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170702 | ||||||
chr18:80170756
|
A | T | 1 | a0001c0008t0006g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.296-10150T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170756 | ||||||
chr18:80170765
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.296-10159C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80170765 | ||||||
chr18:80171161
|
T | C | 2 | a0001c0001t0022g0091a0001c0001t0027g0368 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.296-10555A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171161 | ||||||
chr18:80171165
|
C | T | 36 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(33): Show | 37 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.296-10559G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171165 | ||||||
chr18:80171221
|
A | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.296-10615T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171221 | ||||||
chr18:80171382
|
C | T | 4 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0002t0011g0010others(1): Show | 5 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-10776G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171382 | ||||||
chr18:80171446
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0295a0001c0002t0001g0346 | 3 | HG00558.hp2 NA19054.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.296-10840T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171446 | ||||||
chr18:80171575
|
C | T | 1 | a0001c0001t0002g0137 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.296-10969G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80171575 | ||||||
chr18:80172008
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.296-11402C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172008 | ||||||
chr18:80172166
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.296-11560G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172166 | ||||||
chr18:80172167
|
G | A | 3 | a0001c0001t0002g0125a0001c0001t0002g0139a0001c0001t0002g0173 | 3 | HG02015.hp1 NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.296-11561C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172167 | ||||||
chr18:80172373
|
G | C | 1 | a0001c0001t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.296-11767C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172373 | ||||||
chr18:80172379
|
C | CT | 22 | a0001c0001t0002g0156a0001c0001t0003g0028a0001c0001t0003g0036others(19): Show | 23 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-11774dupA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172379 | ||||||
chr18:80172379
|
CT | C | 8 | a0001c0001t0004g0217a0001c0001t0005g0234a0001c0001t0005g0235others(5): Show | 8 | HG00738.hp1 HG01256.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-11774delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172379 | ||||||
chr18:80172670
|
C | T | 67 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(64): Show | 68 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.296-12064G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172670 | ||||||
chr18:80172727
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.296-12121C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172727 | ||||||
chr18:80172733
|
G | C | 1 | a0001c0001t0004g0196 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.296-12127C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172733 | ||||||
chr18:80172779
|
G | T | 1 | a0001c0001t0008g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.296-12173C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172779 | ||||||
chr18:80172934
|
C | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.296-12328G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80172934 | ||||||
chr18:80173034
|
T | G | 1 | a0001c0001t0005g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.296-12428A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173034 | ||||||
chr18:80173181
|
C | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(151): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.296-12575G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173181 | ||||||
chr18:80173248
|
A | C | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-12642T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173248 | ||||||
chr18:80173250
|
G | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-12644C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173250 | ||||||
chr18:80173270
|
A | G | 1 | a0001c0002t0001g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-12664T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173270 | ||||||
chr18:80173368
|
T | C | 73 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-12762A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173368 | ||||||
chr18:80173439
|
A | G | 1 | a0001c0001t0005g0242 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.296-12833T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173439 | ||||||
chr18:80173556
|
C | T | 6 | a0001c0001t0002g0127a0001c0001t0002g0132a0001c0001t0002g0140others(3): Show | 6 | HG01261.hp1 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-12950G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173556 | ||||||
chr18:80173623
|
TA | T | 73 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-13018delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173623 | ||||||
chr18:80173628
|
A | C | 1 | a0001c0001t0005g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-13022T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173628 | ||||||
chr18:80173715
|
C | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-13109G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173715 | ||||||
chr18:80173834
|
G | A | 3 | a0001c0001t0002g0125a0001c0001t0002g0139a0001c0001t0002g0173 | 3 | HG02015.hp1 NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.296-13228C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173834 | ||||||
chr18:80173845
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.296-13239G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80173845 | ||||||
chr18:80174028
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.296-13422C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174028 | ||||||
chr18:80174453
|
C | A | 42 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(39): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-13847G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174453 | ||||||
chr18:80174521
|
A | G | 31 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0194others(28): Show | 33 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.296-13915T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174521 | ||||||
chr18:80174696
|
T | G | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-14090A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174696 | ||||||
chr18:80174700
|
A | G | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-14094T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174700 | ||||||
chr18:80174701
|
T | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-14095A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174701 | ||||||
chr18:80174720
|
C | T | 8 | a0001c0001t0006g0258a0001c0002t0006g0269a0001c0002t0006g0270others(5): Show | 8 | HG01255.hp1 HG01255.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-14114G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174720 | ||||||
chr18:80174730
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(111): Show | 119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.296-14124C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174730 | ||||||
chr18:80174742
|
CAGG | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0008g0080others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-14139_296-1413 others(7): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174742 | ||||||
chr18:80174810
|
C | T | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-14204G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174810 | ||||||
chr18:80174822
|
C | T | 1 | a0001c0001t0004g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.296-14216G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174822 | ||||||
chr18:80174826
|
C | T | 5 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0026g0084others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-14220G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174826 | ||||||
chr18:80174846
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.296-14240G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174846 | ||||||
chr18:80174928
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.296-14322C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80174928 | ||||||
chr18:80175141
|
A | G | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-14535T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175141 | ||||||
chr18:80175351
|
G | A | 1 | a0001c0002t0006g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.296-14745C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175351 | ||||||
chr18:80175435
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.296-14829G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175435 | ||||||
chr18:80175525
|
C | A | 1 | a0001c0001t0005g0340 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.296-14919G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175525 | ||||||
chr18:80175572
|
C | T | 6 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0026g0084others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-14966G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175572 | ||||||
chr18:80175575
|
C | T | 1 | a0001c0001t0005g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.296-14969G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175575 | ||||||
chr18:80175607
|
G | A | 1 | a0001c0001t0003g0034 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.296-15001C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175607 | ||||||
chr18:80175610
|
C | G | 1 | a0001c0001t0008g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.296-15004G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175610 | ||||||
chr18:80175614
|
G | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.296-15008C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175614 | ||||||
chr18:80175684
|
G | A | 1 | a0001c0001t0005g0342 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.296-15078C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175684 | ||||||
chr18:80175756
|
C | G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-15150G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175756 | ||||||
chr18:80175876
|
G | A | 1 | a0001c0002t0001g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-15270C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175876 | ||||||
chr18:80175930
|
T | C | 1 | a0001c0001t0005g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.296-15324A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80175930 | ||||||
chr18:80176484
|
C | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.296-15878G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176484 | ||||||
chr18:80176532
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.296-15926T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176532 | ||||||
chr18:80176705
|
T | C | 8 | a0001c0001t0004g0195a0001c0001t0004g0197a0001c0001t0004g0200others(5): Show | 8 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-16099A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176705 | ||||||
chr18:80176788
|
G | A | 73 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.296-16182C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176788 | ||||||
chr18:80176906
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.296-16300A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176906 | ||||||
chr18:80176915
|
A | G | 1 | a0001c0002t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.296-16309T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176915 | ||||||
chr18:80176955
|
A | G | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.296-16349T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80176955 | ||||||
chr18:80177016
|
C | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-16410G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177016 | ||||||
chr18:80177023
|
G | A | 2 | a0001c0001t0005g0248a0001c0001t0005g0249 | 2 | HG01517.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.296-16417C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177023 | ||||||
chr18:80177024
|
T | C | 2 | a0001c0001t0005g0248a0001c0001t0005g0249 | 2 | HG01517.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.296-16418A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177024 | ||||||
chr18:80177025
|
G | A | 2 | a0001c0001t0005g0248a0001c0001t0005g0249 | 2 | HG01517.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.296-16419C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177025 | ||||||
chr18:80177025
|
G | GCA | 153 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(150): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.296-16421_296-1642 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177025 | ||||||
chr18:80177025
|
G | GCACA | 58 | a0001c0001t0001g0295a0001c0001t0003g0028a0001c0001t0004g0213others(55): Show | 59 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.296-16423_296-1642 others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177025 | ||||||
chr18:80177025
|
G | GCACACA | 8 | a0001c0001t0004g0001a0001c0001t0004g0199a0001c0001t0004g0210others(5): Show | 10 | HG03225.hp2 HG03669.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.296-16425_296-1642 others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177025 | ||||||
chr18:80177025
|
GCA | G | 5 | a0001c0001t0004g0227a0001c0001t0008g0019a0001c0001t0027g0368others(2): Show | 5 | HG01081.hp1 HG02109.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-16421_296-1642 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177025 | ||||||
chr18:80177051
|
C | G | 1 | a0001c0002t0001g0296 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.296-16445G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177051 | ||||||
chr18:80177068
|
C | A | 1 | a0001c0001t0002g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.296-16462G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177068 | ||||||
chr18:80177081
|
C | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-16475G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177081 | ||||||
chr18:80177084
|
A | G | 2 | a0001c0001t0005g0243a0001c0001t0005g0251 | 2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.296-16478T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177084 | ||||||
chr18:80177097
|
C | T | 6 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0026g0084others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-16491G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177097 | ||||||
chr18:80177170
|
C | CACACAT | 271 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.296-16570_296-1656 others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177170 | ||||||
chr18:80177218
|
G | GCA | 27 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0100others(24): Show | 27 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-16614_296-1661 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACA | 48 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0297others(45): Show | 50 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.296-16616_296-1661 others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACACA | 61 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0025others(58): Show | 65 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.296-16618_296-1661 others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACACAC others(1): Show |
77 | a0001c0001t0001g0287a0001c0001t0001g0293a0001c0001t0001g0295others(74): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.296-16620_296-1661 others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACACAC others(3): Show |
31 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0027others(28): Show | 31 | HG01123.hp1 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.296-16622_296-1661 others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACACAC others(5): Show |
2 | a0001c0001t0032g0067a0001c0002t0001g0304 | 2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-16624_296-1661 others(16): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177218
|
G | GCACACAC others(7): Show |
1 | a0001c0002t0001g0294 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.296-16626_296-1661 others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177218 | ||||||
chr18:80177245
|
C | CACACACA others(3): Show |
1 | a0001c0001t0003g0038 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.296-16640_296-1663 others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177245 | ||||||
chr18:80177262
|
C | G | 5 | a0001c0001t0002g0003a0001c0001t0002g0107a0001c0001t0002g0117others(2): Show | 6 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-16656G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177262 | ||||||
chr18:80177274
|
A | G | 1 | a0001c0001t0005g0246 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.296-16668T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177274 | ||||||
chr18:80177289
|
C | T | 1 | a0001c0002t0006g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.296-16683G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177289 | ||||||
chr18:80177361
|
T | TAC | 21 | a0001c0001t0004g0001a0001c0001t0004g0195a0001c0001t0004g0196others(18): Show | 23 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.296-16757_296-1675 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177361 | ||||||
chr18:80177429
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.296-16823C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177429 | ||||||
chr18:80177445
|
C | T | 271 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.296-16839G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177445 | ||||||
chr18:80177490
|
A | G | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-16884T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177490 | ||||||
chr18:80177782
|
G | T | 1 | a0001c0001t0005g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-17176C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177782 | ||||||
chr18:80177783
|
C | T | 1 | a0001c0001t0005g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-17177G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177783 | ||||||
chr18:80177918
|
G | C | 1 | a0001c0002t0001g0311 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.296-17312C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177918 | ||||||
chr18:80177964
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.296-17358G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177964 | ||||||
chr18:80177972
|
T | TAC | 67 | a0001c0001t0002g0110a0001c0001t0002g0135a0001c0001t0003g0044others(64): Show | 69 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.296-17368_296-1736 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACAC | 39 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0023others(36): Show | 40 | HG00099.hp1 HG00597.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.296-17370_296-1736 others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACAC | 111 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(108): Show | 114 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.296-17372_296-1736 others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACACA others(1): Show |
19 | a0001c0001t0003g0057a0001c0001t0004g0259a0001c0001t0006g0258others(16): Show | 19 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.296-17374_296-1736 others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACACA others(3): Show |
4 | a0001c0002t0006g0078a0001c0002t0006g0274a0001c0002t0006g0351others(1): Show | 4 | HG03041.hp1 HG03453.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-17376_296-1736 others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACACA others(5): Show |
1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.296-17378_296-1736 others(16): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACACA others(7): Show |
1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-17380_296-1736 others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACACACA others(9): Show |
1 | a0001c0002t0006g0350 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.296-17382_296-1736 others(20): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACATACA others(5): Show |
3 | a0001c0001t0004g0194a0001c0001t0004g0214a0001c0004t0004g0190 | 3 | HG01168.hp2 HG01192.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.296-17367_296-1736 others(16): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACATACA others(7): Show |
8 | a0001c0001t0004g0187a0001c0001t0004g0204a0001c0001t0004g0206others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-17367_296-1736 others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACATACA others(9): Show |
21 | a0001c0001t0004g0001a0001c0001t0004g0189a0001c0001t0004g0196others(18): Show | 23 | HG01109.hp2 HG01123.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-17367_296-1736 others(20): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACATACA others(11): Show |
7 | a0001c0001t0004g0191a0001c0001t0004g0195a0001c0001t0004g0201others(4): Show | 7 | HG02572.hp2 HG02602.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-17367_296-1736 others(22): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
T | TACATACA others(21): Show |
1 | a0001c0001t0004g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.296-17367_296-1736 others(32): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80177972
|
TAC | T | 5 | a0001c0001t0002g0151a0001c0001t0002g0161a0001c0001t0002g0184others(2): Show | 5 | HG02258.hp1 HG03209.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-17368_296-1736 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80177972 | ||||||
chr18:80178002
|
C | G | 1 | a0001c0001t0004g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.296-17396G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178002 | ||||||
chr18:80178026
|
C | T | 1 | a0001c0002t0001g0264 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.296-17420G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178026 | ||||||
chr18:80178134
|
G | A | 5 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0026g0084others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-17528C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178134 | ||||||
chr18:80178331
|
G | A | 40 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(37): Show | 41 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.296-17725C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178331 | ||||||
chr18:80178343
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.296-17737G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178343 | ||||||
chr18:80178410
|
C | T | 1 | a0001c0001t0020g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.296-17804G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178410 | ||||||
chr18:80178830
|
AC | A | 156 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(153): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.296-18225delG | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178830 | ||||||
chr18:80178858
|
A | C | 42 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(39): Show | 44 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-18252T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178858 | ||||||
chr18:80178869
|
T | C | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.296-18263A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178869 | ||||||
chr18:80178889
|
A | G | 277 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(274): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.296-18283T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178889 | ||||||
chr18:80178987
|
C | T | 4 | a0001c0002t0006g0278a0001c0002t0006g0313a0001c0002t0006g0314others(1): Show | 4 | HG02486.hp1 HG02723.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-18381G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178987 | ||||||
chr18:80178994
|
G | A | 42 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(39): Show | 44 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-18388C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178994 | ||||||
chr18:80178995
|
C | A | 42 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(39): Show | 44 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-18389G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80178995 | ||||||
chr18:80179048
|
C | A | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-18442G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179048 | ||||||
chr18:80179117
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-18511G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179117 | ||||||
chr18:80179177
|
G | A | 15 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0025others(12): Show | 15 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.296-18571C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179177 | ||||||
chr18:80179223
|
A | AT | 44 | a0001c0001t0002g0115a0001c0001t0002g0146a0001c0001t0002g0162others(41): Show | 45 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.296-18618dupA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179223 | ||||||
chr18:80179223
|
AT | A | 11 | a0001c0001t0002g0110a0001c0001t0002g0157a0001c0001t0005g0335others(8): Show | 11 | HG00597.hp1 HG01081.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.296-18618delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179223 | ||||||
chr18:80179223
|
ATT | A | 45 | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0004g0001others(42): Show | 47 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.296-18619_296-1861 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179223 | ||||||
chr18:80179245
|
T | C | 1 | a0001c0002t0001g0009 | 2 | NA19009.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.296-18639A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179245 | ||||||
chr18:80179277
|
G | A | 1 | a0001c0001t0004g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.296-18671C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179277 | ||||||
chr18:80179303
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.296-18697G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179303 | ||||||
chr18:80179378
|
T | C | 84 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(81): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-18772A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179378 | ||||||
chr18:80179481
|
A | G | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-18875T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179481 | ||||||
chr18:80179634
|
A | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.296-19028T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179634 | ||||||
chr18:80179647
|
C | T | 1 | a0002c0006t0028g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-19041G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179647 | ||||||
chr18:80179756
|
G | A | 1 | a0001c0002t0001g0262 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.296-19150C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179756 | ||||||
chr18:80179983
|
T | C | 276 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.296-19377A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179983 | ||||||
chr18:80179994
|
A | G | 43 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0189others(40): Show | 45 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.296-19388T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80179994 | ||||||
chr18:80180047
|
C | T | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.296-19441G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180047 | ||||||
chr18:80180058
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.296-19452A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180058 | ||||||
chr18:80180141
|
C | T | 1 | a0001c0001t0024g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-19535G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180141 | ||||||
chr18:80180146
|
C | T | 1 | a0002c0006t0028g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-19540G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180146 | ||||||
chr18:80180206
|
C | T | 1 | a0001c0002t0001g0361 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.296-19600G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180206 | ||||||
chr18:80180322
|
C | T | 79 | a0001c0001t0001g0293a0001c0001t0003g0002a0001c0001t0003g0020others(76): Show | 81 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.296-19716G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180322 | ||||||
chr18:80180466
|
G | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0066 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.296-19860C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80180466 | ||||||
chr18:80181018
|
G | A | 67 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(64): Show | 69 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.296-20412C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181018 | ||||||
chr18:80181099
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-20493C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181099 | ||||||
chr18:80181299
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.296-20693C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181299 | ||||||
chr18:80181354
|
C | A | 1 | a0001c0001t0007g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.296-20748G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181354 | ||||||
chr18:80181390
|
G | T | 1 | a0001c0002t0001g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-20784C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181390 | ||||||
chr18:80181477
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0130 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.296-20871G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181477 | ||||||
chr18:80181489
|
C | T | 1 | a0002c0006t0028g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-20883G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181489 | ||||||
chr18:80181690
|
A | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+21020T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181690 | ||||||
chr18:80181842
|
C | T | 1 | a0001c0001t0014g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+20868G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181842 | ||||||
chr18:80181864
|
G | T | 1 | a0001c0001t0002g0124 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.295+20846C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181864 | ||||||
chr18:80181892
|
G | T | 104 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(101): Show | 108 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.295+20818C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80181892 | ||||||
chr18:80182033
|
G | A | 17 | a0001c0001t0001g0293a0001c0002t0001g0006a0001c0002t0001g0275others(14): Show | 18 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.295+20677C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182033 | ||||||
chr18:80182058
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+20652C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182058 | ||||||
chr18:80182374
|
A | G | 1 | a0001c0001t0005g0340 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.295+20336T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182374 | ||||||
chr18:80182505
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+20205G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182505 | ||||||
chr18:80182521
|
A | G | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+20189T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182521 | ||||||
chr18:80182545
|
T | A | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+20165A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182545 | ||||||
chr18:80182601
|
T | A | 65 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(62): Show | 66 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.295+20109A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182601 | ||||||
chr18:80182668
|
C | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0294 | 2 | HG01123.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.295+20042G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182668 | ||||||
chr18:80182684
|
T | C | 1 | a0001c0001t0004g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.295+20026A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182684 | ||||||
chr18:80182722
|
G | T | 67 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(64): Show | 68 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.295+19988C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182722 | ||||||
chr18:80182917
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+19793G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182917 | ||||||
chr18:80182918
|
G | A | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.295+19792C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80182918 | ||||||
chr18:80183015
|
G | A | 1 | a0001c0001t0004g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.295+19695C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183015 | ||||||
chr18:80183053
|
C | G | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.295+19657G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183053 | ||||||
chr18:80183272
|
C | T | 2 | a0001c0004t0004g0190a0001c0004t0004g0192 | 2 | HG03492.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.295+19438G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183272 | ||||||
chr18:80183344
|
G | C | 2 | a0001c0001t0002g0101a0001c0002t0002g0102 | 2 | NA19076.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.295+19366C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183344 | ||||||
chr18:80183507
|
C | T | 3 | a0001c0002t0006g0014a0001c0002t0006g0078a0001c0002t0006g0279 | 3 | HG03041.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.295+19203G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183507 | ||||||
chr18:80183547
|
C | CTCTCTCT others(6): Show |
4 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(1): Show | 5 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+19150_295+1916 others(17): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80183547 | ||||||
chr18:80184007
|
G | A | 10 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.295+18703C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184007 | ||||||
chr18:80184127
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.295+18583C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184127 | ||||||
chr18:80184151
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(53): Show | 57 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.295+18559C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184151 | ||||||
chr18:80184180
|
A | G | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+18530T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184180 | ||||||
chr18:80184445
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+18265G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184445 | ||||||
chr18:80184502
|
G | GCAGAGGG others(19): Show |
1 | a0001c0002t0001g0302 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.295+18207_295+1820 others(30): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184502 | ||||||
chr18:80184502
|
GCAGAGGG others(45): Show |
G | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+18156_295+1820 others(56): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184502 | ||||||
chr18:80184518
|
CGTGAAAC others(19): Show |
C | 6 | a0001c0001t0004g0259a0001c0001t0006g0258a0001c0002t0011g0010others(3): Show | 7 | HG00099.hp2 HG01255.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+18166_295+1819 others(30): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184518 | ||||||
chr18:80184528
|
G | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(102): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.295+18182C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184528 | ||||||
chr18:80184532
|
C | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(102): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.295+18178G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184532 | ||||||
chr18:80184544
|
A | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(108): Show | 117 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.295+18166T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184544 | ||||||
chr18:80184584
|
C | T | 4 | a0001c0001t0005g0231a0001c0001t0005g0236a0001c0001t0005g0245others(1): Show | 4 | HG02735.hp2 HG03491.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+18126G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184584 | ||||||
chr18:80184665
|
T | C | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+18045A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184665 | ||||||
chr18:80184722
|
G | A | 1 | a0001c0008t0006g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.295+17988C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184722 | ||||||
chr18:80184758
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.295+17952T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184758 | ||||||
chr18:80184781
|
G | A | 5 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(2): Show | 5 | HG02056.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+17929C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184781 | ||||||
chr18:80184829
|
G | C | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.295+17881C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80184829 | ||||||
chr18:80185073
|
T | G | 1 | a0001c0001t0004g0363 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.295+17637A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185073 | ||||||
chr18:80185121
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0364 | 3 | NA18979.hp1 NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.295+17589G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185121 | ||||||
chr18:80185232
|
C | T | 13 | a0001c0001t0003g0002a0001c0001t0003g0027a0001c0001t0003g0033others(10): Show | 14 | HG00323.hp1 HG02080.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.295+17478G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185232 | ||||||
chr18:80185309
|
AT | A | 14 | a0001c0001t0001g0183a0001c0001t0002g0122a0001c0001t0008g0080others(11): Show | 14 | HG00639.hp1 HG01243.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.295+17400delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185309 | ||||||
chr18:80185542
|
C | G | 1 | a0001c0001t0002g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.295+17168G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185542 | ||||||
chr18:80185567
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.295+17143C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185567 | ||||||
chr18:80185765
|
T | C | 6 | a0001c0001t0003g0026a0001c0001t0003g0041a0001c0001t0003g0048others(3): Show | 6 | HG01346.hp2 HG01934.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+16945A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185765 | ||||||
chr18:80185774
|
CCT | C | 44 | a0001c0001t0003g0042a0001c0001t0005g0005a0001c0001t0005g0223others(41): Show | 45 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.295+16934_295+1693 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185774 | ||||||
chr18:80185927
|
C | T | 1 | a0001c0002t0006g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.295+16783G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185927 | ||||||
chr18:80185968
|
GCACCCTC others(31): Show |
G | 1 | a0001c0001t0020g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.295+16704_295+1674 others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80185968 | ||||||
chr18:80186004
|
G | A | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+16706C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186004 | ||||||
chr18:80186027
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0107a0001c0001t0002g0117others(2): Show | 6 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+16683G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186027 | ||||||
chr18:80186035
|
T | A | 1 | a0001c0001t0002g0162 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.295+16675A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186035 | ||||||
chr18:80186148
|
G | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(59): Show | 63 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.295+16562C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186148 | ||||||
chr18:80186169
|
C | T | 1 | a0001c0002t0001g0346 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.295+16541G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186169 | ||||||
chr18:80186234
|
G | A | 1 | a0001c0001t0006g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.295+16476C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186234 | ||||||
chr18:80186301
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.295+16409T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186301 | ||||||
chr18:80186343
|
GCATGCAC others(132): Show |
G | 8 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+16228_295+1636 others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186343 | ||||||
chr18:80186353
|
TCACACAT others(11): Show |
T | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.295+16339_295+1635 others(22): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186353 | ||||||
chr18:80186365
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.295+16345C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186365 | ||||||
chr18:80186367
|
ACACCCAC others(112): Show |
A | 2 | a0001c0003t0008g0082a0001c0003t0008g0083 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+16224_295+1634 others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186367 | ||||||
chr18:80186371
|
C | CCT | 260 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(257): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.295+16338_295+1633 others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186371 | ||||||
chr18:80186404
|
C | G | 10 | a0001c0002t0001g0257a0001c0002t0001g0261a0001c0002t0001g0262others(7): Show | 10 | HG00408.hp1 HG00621.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.295+16306G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186404 | ||||||
chr18:80186452
|
C | T | 62 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(59): Show | 63 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.295+16258G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186452 | ||||||
chr18:80186524
|
G | A | 1 | a0001c0002t0006g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295+16186C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186524 | ||||||
chr18:80186527
|
T | C | 2 | a0001c0003t0008g0082a0001c0003t0008g0083 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+16183A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186527 | ||||||
chr18:80186659
|
CATATAA | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.295+16045_295+1605 others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186659 | ||||||
chr18:80186791
|
A | G | 2 | a0001c0001t0004g0194a0001c0001t0004g0214 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.295+15919T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186791 | ||||||
chr18:80186926
|
G | A | 1 | a0001c0002t0001g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.295+15784C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186926 | ||||||
chr18:80186948
|
A | T | 58 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(55): Show | 59 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.295+15762T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186948 | ||||||
chr18:80186955
|
C | T | 4 | a0001c0001t0004g0175a0001c0001t0004g0176a0001c0001t0004g0259others(1): Show | 4 | HG00099.hp2 HG01255.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+15755G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186955 | ||||||
chr18:80186960
|
G | A | 3 | a0001c0001t0012g0058a0001c0001t0012g0061a0001c0001t0012g0062 | 3 | HG01069.hp2 HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.295+15750C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186960 | ||||||
chr18:80186976
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+15734C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186976 | ||||||
chr18:80186997
|
G | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.295+15713C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80186997 | ||||||
chr18:80187099
|
GA | G | 7 | a0001c0001t0002g0122a0001c0001t0004g0196a0001c0001t0005g0250others(4): Show | 7 | HG01243.hp1 HG01515.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+15610delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187099 | ||||||
chr18:80187116
|
G | A | 1 | a0001c0001t0018g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.295+15594C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187116 | ||||||
chr18:80187248
|
G | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+15462C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187248 | ||||||
chr18:80187399
|
T | G | 1 | a0001c0002t0009g0322 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.295+15311A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187399 | ||||||
chr18:80187442
|
T | C | 237 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(234): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.295+15268A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187442 | ||||||
chr18:80187684
|
C | T | 4 | a0001c0002t0001g0276a0001c0002t0001g0289a0001c0002t0001g0291others(1): Show | 4 | HG02040.hp1 NA18947.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+15026G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187684 | ||||||
chr18:80187773
|
G | A | 22 | a0001c0001t0002g0004a0001c0001t0002g0112a0001c0001t0002g0113others(19): Show | 23 | HG00408.hp2 HG00558.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.295+14937C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187773 | ||||||
chr18:80187911
|
T | C | 1 | a0001c0002t0001g0265 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.295+14799A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80187911 | ||||||
chr18:80188007
|
G | A | 2 | a0001c0001t0007g0169a0001c0001t0007g0170 | 2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.295+14703C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188007 | ||||||
chr18:80188028
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+14682G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188028 | ||||||
chr18:80188082
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.295+14628G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188082 | ||||||
chr18:80188090
|
G | A | 12 | a0001c0002t0001g0013a0001c0002t0001g0352a0001c0002t0001g0353others(9): Show | 12 | HG00673.hp2 HG01928.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+14620C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188090 | ||||||
chr18:80188103
|
A | G | 3 | a0001c0001t0004g0216a0001c0001t0004g0217a0001c0001t0004g0218 | 3 | HG02572.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.295+14607T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188103 | ||||||
chr18:80188353
|
G | T | 2 | a0001c0001t0005g0332a0001c0001t0005g0333 | 2 | HG00621.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.295+14357C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80188353 | ||||||
chr18:80189216
|
G | A | 23 | a0001c0001t0002g0004a0001c0001t0002g0098a0001c0001t0002g0112others(20): Show | 24 | HG00408.hp2 HG00558.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.295+13494C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189216 | ||||||
chr18:80189378
|
C | T | 3 | a0001c0001t0004g0229a0001c0001t0017g0226a0001c0001t0023g0228 | 3 | HG02976.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.295+13332G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189378 | ||||||
chr18:80189399
|
G | A | 5 | a0001c0001t0003g0024a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+13311C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189399 | ||||||
chr18:80189545
|
C | T | 1 | a0001c0001t0005g0343 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.295+13165G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189545 | ||||||
chr18:80189653
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.295+13057C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189653 | ||||||
chr18:80189687
|
C | T | 1 | a0001c0002t0006g0269 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.295+13023G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80189687 | ||||||
chr18:80190109
|
G | A | 4 | a0001c0001t0003g0002a0001c0001t0003g0033a0001c0001t0003g0034others(1): Show | 5 | NA18967.hp2 NA18979.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+12601C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80190109 | ||||||
chr18:80190114
|
C | G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295+12596G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80190114 | ||||||
chr18:80190271
|
CA | C | 271 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.295+12438delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80190271 | ||||||
chr18:80190452
|
T | C | 45 | a0001c0001t0004g0221a0001c0001t0004g0222a0001c0001t0005g0005others(42): Show | 46 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.295+12258A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80190452 | ||||||
chr18:80190897
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+11813G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80190897 | ||||||
chr18:80191049
|
G | A | 1 | a0001c0001t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.295+11661C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191049 | ||||||
chr18:80191077
|
G | C | 53 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0043others(50): Show | 55 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.295+11633C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191077 | ||||||
chr18:80191205
|
T | C | 74 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(71): Show | 75 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.295+11505A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191205 | ||||||
chr18:80191309
|
C | G | 1 | a0001c0001t0007g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+11401G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191309 | ||||||
chr18:80191353
|
C | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(59): Show | 63 | HG00323.hp1 HG00438.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.295+11357G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191353 | ||||||
chr18:80191369
|
T | TC | 10 | a0001c0001t0007g0178a0001c0001t0007g0180a0001c0001t0008g0080others(7): Show | 10 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+11340dupG | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191369 | ||||||
chr18:80191393
|
G | C | 6 | a0001c0001t0007g0178a0001c0001t0007g0180a0001c0001t0010g0086others(3): Show | 6 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+11317C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191393 | ||||||
chr18:80191406
|
T | G | 1 | a0001c0001t0002g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.295+11304A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191406 | ||||||
chr18:80191520
|
G | A | 1 | a0001c0001t0005g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.295+11190C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191520 | ||||||
chr18:80191581
|
G | A | 3 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0031 | 3 | HG02056.hp2 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.295+11129C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191581 | ||||||
chr18:80191676
|
C | A | 1 | a0001c0001t0002g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.295+11034G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191676 | ||||||
chr18:80191713
|
C | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(109): Show | 117 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.295+10997G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191713 | ||||||
chr18:80191939
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.295+10771T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80191939 | ||||||
chr18:80192164
|
G | A | 1 | a0001c0002t0001g0009 | 2 | NA19009.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.295+10546C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192164 | ||||||
chr18:80192417
|
T | TGGGAGCC others(30): Show |
8 | a0001c0001t0004g0363a0001c0001t0008g0080a0001c0001t0008g0085others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+10256_295+1029 others(41): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192417 | ||||||
chr18:80192417
|
T | TGGGAGCC others(104): Show |
5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+10182_295+1029 others(115): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192417 | ||||||
chr18:80192419
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.295+10291C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192419 | ||||||
chr18:80192432
|
C | T | 43 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.295+10278G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192432 | ||||||
chr18:80192455
|
G | A | 1 | a0001c0001t0004g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.295+10255C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192455 | ||||||
chr18:80192506
|
CGGGGGAG others(30): Show |
C | 5 | a0001c0001t0003g0024a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+10167_295+1020 others(41): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192506 | ||||||
chr18:80192507
|
G | A | 2 | a0001c0001t0007g0169a0001c0001t0007g0170 | 2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.295+10203C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192507 | ||||||
chr18:80192555
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0018g0154 | 2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.295+10155C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192555 | ||||||
chr18:80192652
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+10058G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192652 | ||||||
chr18:80192660
|
T | C | 228 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(225): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.295+10050A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192660 | ||||||
chr18:80192785
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0199a0001c0001t0004g0210others(3): Show | 8 | NA18955.hp2 NA18957.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+9925C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192785 | ||||||
chr18:80192942
|
T | A | 1 | a0001c0001t0020g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.295+9768A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80192942 | ||||||
chr18:80193161
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.295+9549C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193161 | ||||||
chr18:80193170
|
G | A | 58 | a0001c0001t0002g0100a0001c0001t0002g0108a0001c0001t0002g0109others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.295+9540C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193170 | ||||||
chr18:80193209
|
G | T | 1 | a0001c0001t0005g0223 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.295+9501C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193209 | ||||||
chr18:80193632
|
T | C | 14 | a0001c0001t0003g0036a0001c0001t0003g0366a0001c0001t0008g0080others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.295+9078A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193632 | ||||||
chr18:80193738
|
G | C | 2 | a0001c0001t0002g0101a0001c0002t0002g0102 | 2 | NA19076.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.295+8972C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193738 | ||||||
chr18:80193888
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.295+8822C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80193888 | ||||||
chr18:80194328
|
A | C | 2 | a0001c0001t0005g0240a0001c0001t0005g0241 | 2 | HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.295+8382T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194328 | ||||||
chr18:80194588
|
C | G | 1 | a0001c0001t0005g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.295+8122G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194588 | ||||||
chr18:80194597
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.295+8113C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194597 | ||||||
chr18:80194756
|
A | C | 72 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(69): Show | 73 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+7954T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194756 | ||||||
chr18:80194850
|
A | C | 62 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(59): Show | 63 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.295+7860T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194850 | ||||||
chr18:80194950
|
C | T | 1 | a0001c0001t0005g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.295+7760G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194950 | ||||||
chr18:80194961
|
C | T | 2 | a0001c0001t0005g0239a0001c0001t0005g0242 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.295+7749G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80194961 | ||||||
chr18:80195035
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.295+7675G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195035 | ||||||
chr18:80195044
|
G | GACT | 370 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(367): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.295+7665_295+7666i others(5): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195044 | ||||||
chr18:80195097
|
C | T | 1 | a0001c0001t0010g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.295+7613G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195097 | ||||||
chr18:80195195
|
A | T | 3 | a0001c0002t0006g0014a0001c0002t0006g0078a0001c0002t0006g0279 | 3 | HG03041.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.295+7515T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195195 | ||||||
chr18:80195252
|
G | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(59): Show | 63 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.295+7458C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195252 | ||||||
chr18:80195329
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+7381C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195329 | ||||||
chr18:80195437
|
C | A | 1 | a0001c0001t0002g0129 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.295+7273G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195437 | ||||||
chr18:80195469
|
G | A | 1 | a0001c0002t0006g0269 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.295+7241C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195469 | ||||||
chr18:80195544
|
G | GATATATA others(11): Show |
1 | a0001c0002t0001g0346 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.295+7165_295+7166i others(20): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195544 | ||||||
chr18:80195544
|
G | GATATATA others(27): Show |
1 | a0001c0002t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.295+7165_295+7166i others(36): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195544 | ||||||
chr18:80195548
|
C | CAT | 23 | a0001c0001t0002g0004a0001c0001t0002g0098a0001c0001t0002g0107others(20): Show | 24 | HG00558.hp1 HG01106.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.295+7160_295+7161d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATACATA others(29): Show |
2 | a0001c0002t0001g0358a0001c0002t0001g0359 | 2 | NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.295+7161_295+7162i others(38): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATAT | 10 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0123others(7): Show | 10 | HG00408.hp2 HG02135.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+7158_295+7161d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATAT | 5 | a0001c0001t0004g0217a0001c0001t0005g0223a0001c0001t0005g0235others(2): Show | 5 | HG01169.hp1 HG01256.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+7156_295+7161d others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(24): Show |
1 | a0001c0002t0001g0257 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.295+7161_295+7162i others(33): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(1): Show |
6 | a0001c0001t0002g0150a0001c0001t0002g0163a0001c0001t0004g0216others(3): Show | 6 | HG02572.hp2 HG03540.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+7154_295+7161d others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(3): Show |
11 | a0001c0001t0003g0182a0001c0001t0007g0120a0001c0001t0007g0130others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.295+7152_295+7161d others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(5): Show |
13 | a0001c0001t0001g0293a0001c0001t0003g0046a0001c0001t0007g0021others(10): Show | 13 | HG00423.hp1 HG01074.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.295+7150_295+7161d others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(7): Show |
3 | a0001c0001t0005g0253a0001c0001t0007g0131a0001c0002t0013g0012 | 3 | HG02897.hp1 HG06807.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.295+7148_295+7161d others(16): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(9): Show |
13 | a0001c0001t0004g0176a0001c0001t0005g0224a0001c0001t0005g0232others(10): Show | 13 | HG01175.hp1 HG01257.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.295+7146_295+7161d others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(11): Show |
16 | a0001c0001t0004g0175a0001c0001t0005g0005a0001c0001t0005g0233others(13): Show | 17 | HG00438.hp1 HG01496.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+7144_295+7161d others(20): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(13): Show |
24 | a0001c0001t0004g0259a0001c0001t0005g0234a0001c0001t0005g0236others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+7142_295+7161d others(22): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(15): Show |
8 | a0001c0001t0005g0340a0001c0001t0006g0258a0001c0001t0027g0368others(5): Show | 8 | HG01255.hp2 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+7140_295+7161d others(24): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(17): Show |
9 | a0001c0001t0005g0231a0001c0001t0005g0241a0001c0002t0001g0291others(6): Show | 9 | HG01074.hp2 HG03041.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+7138_295+7161d others(26): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(19): Show |
3 | a0001c0001t0005g0335a0001c0002t0001g0290a0001c0002t0009g0321 | 3 | NA18945.hp2 NA18973.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.295+7161_295+7162i others(28): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(21): Show |
7 | a0001c0001t0005g0339a0001c0002t0001g0133a0001c0002t0001g0134others(4): Show | 7 | HG01256.hp1 HG02040.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(30): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(23): Show |
5 | a0001c0002t0001g0262a0001c0002t0001g0265a0001c0002t0001g0267others(2): Show | 5 | HG00621.hp1 HG01346.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(32): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(25): Show |
4 | a0001c0002t0001g0288a0001c0002t0001g0308a0001c0002t0001g0324others(1): Show | 4 | HG00408.hp1 NA18939.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(34): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(27): Show |
5 | a0001c0001t0005g0249a0001c0002t0001g0277a0001c0002t0001g0301others(2): Show | 5 | HG02056.hp1 HG03654.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(36): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(29): Show |
4 | a0001c0002t0001g0009a0001c0002t0001g0275a0001c0002t0001g0306others(1): Show | 5 | HG02300.hp2 NA18952.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(38): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(31): Show |
6 | a0001c0001t0001g0329a0001c0002t0001g0261a0001c0002t0001g0264others(3): Show | 6 | HG00673.hp2 NA18942.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+7161_295+7162i others(40): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(33): Show |
1 | a0001c0002t0001g0328 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.295+7161_295+7162i others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(37): Show |
1 | a0001c0002t0001g0352 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.295+7161_295+7162i others(46): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | CATATATA others(41): Show |
2 | a0001c0002t0001g0263a0001c0002t0001g0323 | 2 | HG00099.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.295+7161_295+7162i others(50): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
C | T | 2 | a0001c0002t0001g0331a0001c0002t0001g0346 | 2 | HG03831.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.295+7162G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
CAT | C | 3 | a0001c0002t0001g0006a0001c0002t0001g0280a0001c0002t0001g0364 | 4 | HG01952.hp1 NA18979.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+7160_295+7161d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195548
|
CATATAT | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0295a0001c0001t0005g0245others(5): Show | 9 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+7156_295+7161d others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195548 | ||||||
chr18:80195557
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0004g0197a0001c0001t0004g0202 | 2 | HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.295+7152_295+7153i others(40): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195557 | ||||||
chr18:80195559
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0004g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.295+7150_295+7151i others(34): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(55): Show |
1 | a0001c0001t0004g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.295+7150_295+7151i others(64): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0004g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.295+7150_295+7151i others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(29): Show |
24 | a0001c0001t0004g0001a0001c0001t0004g0187a0001c0001t0004g0195others(21): Show | 26 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.295+7150_295+7151i others(38): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(31): Show |
8 | a0001c0001t0004g0193a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 8 | HG00438.hp2 HG01168.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+7150_295+7151i others(40): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(33): Show |
2 | a0001c0001t0004g0194a0001c0004t0004g0192 | 2 | HG01192.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.295+7150_295+7151i others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195559
|
A | ATATATAT others(69): Show |
1 | a0001c0001t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.295+7150_295+7151i others(78): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195559 | ||||||
chr18:80195566
|
TATATATA others(1): Show |
T | 17 | a0001c0001t0003g0028a0001c0001t0003g0035a0001c0001t0003g0036others(14): Show | 17 | HG01069.hp2 HG01884.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+7136_295+7143d others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195566 | ||||||
chr18:80195568
|
TATATAC | T | 39 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(36): Show | 40 | HG00323.hp1 HG01081.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.295+7136_295+7141d others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195568 | ||||||
chr18:80195570
|
T | TATATATA others(24): Show |
1 | a0001c0002t0001g0330 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.295+7139_295+7140i others(33): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195570 | ||||||
chr18:80195570
|
TATAC | T | 6 | a0001c0001t0003g0038a0001c0001t0003g0040a0001c0001t0003g0047others(3): Show | 6 | HG02886.hp1 NA18999.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+7136_295+7139d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195570 | ||||||
chr18:80195572
|
T | C | 2 | a0001c0002t0001g0358a0001c0002t0001g0359 | 2 | NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.295+7138A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(5): Show |
2 | a0001c0001t0022g0091a0001c0001t0030g0266 | 2 | HG02273.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.295+7137_295+7138i others(14): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(9): Show |
2 | a0001c0002t0001g0284a0001c0002t0013g0011 | 2 | HG02258.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.295+7137_295+7138i others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(11): Show |
1 | a0001c0002t0011g0371 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.295+7137_295+7138i others(20): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(13): Show |
1 | a0001c0001t0005g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.295+7137_295+7138i others(22): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(15): Show |
2 | a0001c0002t0011g0370a0001c0002t0015g0186 | 2 | HG00642.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.295+7137_295+7138i others(24): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(17): Show |
2 | a0001c0002t0011g0010a0001c0002t0015g0185 | 3 | HG00738.hp1 HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.295+7137_295+7138i others(26): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(19): Show |
1 | a0001c0002t0001g0347 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.295+7137_295+7138i others(28): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(27): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0002t0001g0282 | 4 | HG00639.hp1 HG01257.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+7137_295+7138i others(36): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(29): Show |
2 | a0001c0001t0001g0298a0001c0002t0001g0348 | 2 | HG01943.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.295+7137_295+7138i others(38): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(31): Show |
1 | a0001c0001t0001g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.295+7137_295+7138i others(40): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195572
|
T | TATATATA others(33): Show |
1 | a0001c0002t0001g0296 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.295+7137_295+7138i others(42): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195572 | ||||||
chr18:80195574
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+7136G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195574 | ||||||
chr18:80195576
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+7134G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195576 | ||||||
chr18:80195578
|
C | T | 3 | a0001c0003t0008g0082a0001c0003t0008g0083a0002c0006t0028g0081 | 3 | HG02809.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295+7132G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195578 | ||||||
chr18:80195580
|
T | A | 2 | a0001c0003t0008g0082a0001c0003t0008g0083 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+7130A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195580 | ||||||
chr18:80195609
|
G | C | 43 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.295+7101C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195609 | ||||||
chr18:80195657
|
C | T | 1 | a0001c0001t0005g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.295+7053G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195657 | ||||||
chr18:80195797
|
C | T | 1 | a0001c0001t0005g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.295+6913G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195797 | ||||||
chr18:80195814
|
T | G | 1 | a0001c0002t0002g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.295+6896A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195814 | ||||||
chr18:80195880
|
A | G | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.295+6830T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195880 | ||||||
chr18:80195893
|
C | CT | 174 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(171): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.295+6816dupA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80195893 | ||||||
chr18:80196683
|
G | A | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.295+6027C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196683 | ||||||
chr18:80196754
|
C | A | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.295+5956G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196754 | ||||||
chr18:80196875
|
A | G | 1 | a0001c0001t0008g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.295+5835T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196875 | ||||||
chr18:80196890
|
TA | T | 33 | a0001c0001t0002g0101a0001c0001t0002g0107a0001c0001t0002g0149others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.295+5819delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196890 | ||||||
chr18:80196890
|
TAA | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(151): Show | 161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.295+5818_295+5819d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196890 | ||||||
chr18:80196890
|
TAAA | T | 19 | a0001c0001t0002g0110a0001c0001t0004g0191a0001c0001t0004g0193others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.295+5817_295+5819d others(5): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80196890 | ||||||
chr18:80197006
|
CA | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.295+5703delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197006 | ||||||
chr18:80197038
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+5672G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197038 | ||||||
chr18:80197275
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.295+5435C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197275 | ||||||
chr18:80197397
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.295+5313C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197397 | ||||||
chr18:80197443
|
T | C | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+5267A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197443 | ||||||
chr18:80197495
|
C | T | 229 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(226): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.295+5215G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197495 | ||||||
chr18:80197741
|
T | TAGAA | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+4968_295+4969i others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197741 | ||||||
chr18:80197808
|
T | C | 2 | a0001c0001t0007g0169a0001c0001t0007g0170 | 2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.295+4902A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197808 | ||||||
chr18:80197921
|
C | G | 1 | a0001c0001t0004g0225 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.295+4789G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80197921 | ||||||
chr18:80198063
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.295+4647C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198063 | ||||||
chr18:80198172
|
A | C | 229 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(226): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.295+4538T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198172 | ||||||
chr18:80198202
|
T | C | 229 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(226): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.295+4508A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198202 | ||||||
chr18:80198318
|
A | G | 1 | a0001c0001t0026g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.295+4392T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198318 | ||||||
chr18:80198331
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.295+4379C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198331 | ||||||
chr18:80198492
|
G | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.295+4218C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198492 | ||||||
chr18:80198752
|
G | A | 1 | a0001c0002t0006g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295+3958C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80198752 | ||||||
chr18:80199014
|
C | T | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.295+3696G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199014 | ||||||
chr18:80199094
|
T | C | 1 | a0001c0001t0005g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.295+3616A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199094 | ||||||
chr18:80199134
|
G | C | 1 | a0001c0001t0033g0369 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.295+3576C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199134 | ||||||
chr18:80199442
|
G | A | 24 | a0001c0001t0002g0100a0001c0001t0002g0108a0001c0001t0002g0109others(21): Show | 24 | HG00140.hp1 HG00738.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.295+3268C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199442 | ||||||
chr18:80199485
|
T | C | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.295+3225A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199485 | ||||||
chr18:80199558
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.295+3152G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199558 | ||||||
chr18:80199656
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.295+3054A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199656 | ||||||
chr18:80199737
|
G | A | 1 | a0001c0002t0001g0354 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.295+2973C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199737 | ||||||
chr18:80199894
|
C | G | 1 | a0001c0002t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.295+2816G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80199894 | ||||||
chr18:80200195
|
C | G | 14 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0035others(11): Show | 14 | HG01069.hp2 HG01884.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.295+2515G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200195 | ||||||
chr18:80200326
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.295+2384C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200326 | ||||||
chr18:80200358
|
C | A | 1 | a0001c0001t0003g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.295+2352G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200358 | ||||||
chr18:80200461
|
G | A | 1 | a0001c0001t0007g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.295+2249C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200461 | ||||||
chr18:80200498
|
C | T | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+2212G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200498 | ||||||
chr18:80200513
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.295+2197G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200513 | ||||||
chr18:80200623
|
C | T | 1 | a0001c0001t0004g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.295+2087G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200623 | ||||||
chr18:80200763
|
G | A | 1 | a0001c0001t0005g0253 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.295+1947C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200763 | ||||||
chr18:80200865
|
G | A | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295+1845C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200865 | ||||||
chr18:80200959
|
C | A | 3 | a0001c0002t0006g0278a0001c0002t0006g0314a0001c0002t0006g0315 | 3 | HG02486.hp1 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.295+1751G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200959 | ||||||
chr18:80200981
|
G | A | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.295+1729C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200981 | ||||||
chr18:80200999
|
C | A | 2 | a0001c0001t0003g0040a0001c0001t0031g0039 | 2 | NA19054.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.295+1711G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80200999 | ||||||
chr18:80201024
|
C | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(100): Show | 107 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.295+1686G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201024 | ||||||
chr18:80201094
|
G | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+1616C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201094 | ||||||
chr18:80201154
|
A | G | 1 | a0001c0001t0004g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.295+1556T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201154 | ||||||
chr18:80201260
|
T | C | 1 | a0001c0002t0011g0371 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.295+1450A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201260 | ||||||
chr18:80201432
|
G | C | 2 | a0001c0001t0007g0120a0001c0001t0007g0130 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295+1278C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201432 | ||||||
chr18:80201480
|
C | G | 160 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.295+1230G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201480 | ||||||
chr18:80201519
|
T | G | 1 | a0001c0002t0001g0318 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.295+1191A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201519 | ||||||
chr18:80201622
|
A | G | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1088T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201622 | ||||||
chr18:80201635
|
C | T | 6 | a0001c0002t0001g0352a0001c0002t0001g0356a0001c0002t0001g0357others(3): Show | 6 | HG00673.hp2 HG02300.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1075G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201635 | ||||||
chr18:80201636
|
G | A | 1 | a0001c0002t0006g0270 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.295+1074C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201636 | ||||||
chr18:80201695
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.295+1015G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201695 | ||||||
chr18:80201794
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.295+916C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80201794 | ||||||
chr18:80202126
|
AAAC | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(59): Show | 63 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.295+581_295+583del others(3): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202126 | ||||||
chr18:80202298
|
G | A | 1 | a0001c0002t0006g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.295+412C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202298 | ||||||
chr18:80202339
|
C | A | 1 | a0001c0002t0001g0320 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.295+371G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202339 | ||||||
chr18:80202343
|
A | G | 4 | a0001c0001t0005g0005a0001c0001t0005g0246a0001c0001t0005g0250others(1): Show | 5 | NA18957.hp2 NA19055.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+367T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202343 | ||||||
chr18:80202390
|
G | A | 1 | a0001c0001t0005g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.295+320C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202390 | ||||||
chr18:80202400
|
G | C | 48 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0003g0020others(45): Show | 50 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.295+310C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202400 | ||||||
chr18:80202463
|
T | A | 1 | a0001c0002t0001g0013 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.295+247A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202463 | ||||||
chr18:80202516
|
A | G | 1 | a0001c0001t0008g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.295+194T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202516 | ||||||
chr18:80202638
|
G | GA | 156 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(153): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.295+71dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202638 | ||||||
chr18:80202667
|
G | A | 1 | a0001c0002t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.295+43C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202667 | ||||||
chr18:80202688
|
G | A | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+22C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 2/2 | chr18 | 80202688 | ||||||
chr18:80203138
|
C | T | 44 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0004g0001others(41): Show | 46 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.73-206G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203138 | ||||||
chr18:80203352
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.73-420T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203352 | ||||||
chr18:80203429
|
C | T | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.73-497G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203429 | ||||||
chr18:80203464
|
C | T | 43 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.73-532G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203464 | ||||||
chr18:80203646
|
A | G | 72 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(69): Show | 73 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.73-714T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203646 | ||||||
chr18:80203650
|
A | G | 72 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(69): Show | 73 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.73-718T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203650 | ||||||
chr18:80203709
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0130 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.73-777G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203709 | ||||||
chr18:80203785
|
T | A | 2 | a0001c0001t0007g0131a0001c0001t0007g0145 | 2 | HG02897.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.73-853A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203785 | ||||||
chr18:80203785
|
T | C | 1 | a0001c0002t0001g0360 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.73-853A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80203785 | ||||||
chr18:80204468
|
T | C | 1 | a0001c0001t0002g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.73-1536A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204468 | ||||||
chr18:80204606
|
TA | T | 13 | a0001c0001t0002g0004a0001c0001t0002g0099a0001c0001t0002g0122others(10): Show | 14 | HG01074.hp1 HG02647.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-1675delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204606 | ||||||
chr18:80204607
|
A | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-1675T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204607 | ||||||
chr18:80204724
|
A | G | 1 | a0001c0001t0005g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.73-1792T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204724 | ||||||
chr18:80204774
|
C | T | 2 | a0001c0001t0008g0029a0001c0001t0008g0032 | 2 | HG02056.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.73-1842G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204774 | ||||||
chr18:80204801
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.73-1869T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204801 | ||||||
chr18:80204816
|
T | C | 5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-1884A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80204816 | ||||||
chr18:80205015
|
C | T | 4 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0167others(1): Show | 4 | NA18971.hp2 NA18991.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-2083G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205015 | ||||||
chr18:80205209
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.73-2277T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205209 | ||||||
chr18:80205232
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.73-2300C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205232 | ||||||
chr18:80205292
|
A | G | 1 | a0001c0002t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.73-2360T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205292 | ||||||
chr18:80205755
|
T | G | 1 | a0001c0001t0002g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.73-2823A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205755 | ||||||
chr18:80205847
|
T | C | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73-2915A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80205847 | ||||||
chr18:80206083
|
G | C | 59 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(56): Show | 60 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-3151C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206083 | ||||||
chr18:80206376
|
G | A | 1 | a0001c0001t0026g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-3444C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206376 | ||||||
chr18:80206648
|
T | C | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.73-3716A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206648 | ||||||
chr18:80206711
|
C | T | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-3779G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206711 | ||||||
chr18:80206969
|
G | T | 3 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0060 | 3 | HG02630.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.73-4037C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206969 | ||||||
chr18:80206977
|
A | C | 1 | a0002c0006t0028g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-4045T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80206977 | ||||||
chr18:80207013
|
GACTTAAC others(56): Show |
G | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-4144_73-4082del others(63): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207013 | ||||||
chr18:80207015
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.73-4083G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207015 | ||||||
chr18:80207078
|
C | T | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-4146G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207078 | ||||||
chr18:80207166
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-4234G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207166 | ||||||
chr18:80207229
|
A | AGATGTTT others(56): Show |
1 | a0001c0001t0003g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-4360_73-4298dup others(63): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207229 | ||||||
chr18:80207229
|
A | C | 198 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(195): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.73-4297T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207229 | ||||||
chr18:80207229
|
A | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0236a0001c0001t0005g0245 | 3 | HG03491.hp1 HG03669.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.73-4297T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207229 | ||||||
chr18:80207229
|
AGATGTTT others(56): Show |
A | 2 | a0001c0001t0002g0135a0001c0001t0026g0084 | 2 | HG02965.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.73-4360_73-4298del others(63): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207229 | ||||||
chr18:80207365
|
T | C | 1 | a0001c0002t0002g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.73-4433A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207365 | ||||||
chr18:80207467
|
C | T | 39 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(36): Show | 39 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-4535G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207467 | ||||||
chr18:80207994
|
G | T | 3 | a0001c0002t0015g0185a0001c0002t0015g0186a0001c0002t0029g0255 | 3 | HG00642.hp2 HG00738.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.73-5062C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80207994 | ||||||
chr18:80208023
|
GGTATCAA others(25): Show |
G | 1 | a0001c0001t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.73-5123_73-5092del others(32): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208023 | ||||||
chr18:80208023
|
GGTATCAA others(57): Show |
G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-5155_73-5092del others(64): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208023 | ||||||
chr18:80208181
|
A | G | 273 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(270): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.73-5249T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208181 | ||||||
chr18:80208343
|
A | C | 1 | a0001c0002t0001g0355 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.73-5411T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208343 | ||||||
chr18:80208397
|
G | T | 25 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0004g0187others(22): Show | 25 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.73-5465C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208397 | ||||||
chr18:80208458
|
G | T | 4 | a0001c0002t0006g0269a0001c0002t0006g0270a0001c0002t0006g0273others(1): Show | 4 | NA18963.hp1 NA18966.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-5526C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208458 | ||||||
chr18:80208485
|
T | A | 15 | a0001c0002t0001g0006a0001c0002t0001g0275a0001c0002t0001g0280others(12): Show | 16 | HG00099.hp1 HG01099.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.73-5553A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208485 | ||||||
chr18:80208661
|
T | C | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-5729A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208661 | ||||||
chr18:80208738
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-5806C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208738 | ||||||
chr18:80208742
|
A | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-5810T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208742 | ||||||
chr18:80208752
|
T | C | 1 | a0001c0001t0002g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.73-5820A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208752 | ||||||
chr18:80208763
|
A | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 116 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.73-5831T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208763 | ||||||
chr18:80208767
|
A | G | 5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-5835T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208767 | ||||||
chr18:80208805
|
G | A | 40 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(37): Show | 40 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.73-5873C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208805 | ||||||
chr18:80208844
|
C | T | 1 | a0001c0001t0005g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.73-5912G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80208844 | ||||||
chr18:80209011
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73-6079T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209011 | ||||||
chr18:80209124
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0012g0058 | 3 | HG01257.hp2 HG01358.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.73-6192G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209124 | ||||||
chr18:80209124
|
C | CA | 12 | a0001c0001t0003g0182a0001c0001t0007g0021a0001c0001t0010g0086others(9): Show | 12 | HG00438.hp1 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-6193dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209124 | ||||||
chr18:80209128
|
A | C | 51 | a0001c0001t0002g0137a0001c0001t0002g0157a0001c0001t0003g0035others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.73-6196T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209128 | ||||||
chr18:80209136
|
A | C | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-6204T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209136 | ||||||
chr18:80209174
|
T | C | 40 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(37): Show | 40 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.73-6242A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209174 | ||||||
chr18:80209177
|
A | C | 1 | a0001c0002t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.73-6245T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209177 | ||||||
chr18:80209207
|
C | T | 1 | a0001c0002t0001g0328 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.73-6275G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209207 | ||||||
chr18:80209381
|
T | G | 1 | a0001c0001t0004g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.73-6449A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209381 | ||||||
chr18:80209411
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.73-6479A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209411 | ||||||
chr18:80209476
|
A | T | 1 | a0001c0001t0003g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.73-6544T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209476 | ||||||
chr18:80209970
|
C | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-7038G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80209970 | ||||||
chr18:80210003
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-7071G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210003 | ||||||
chr18:80210005
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-7073A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210005 | ||||||
chr18:80210089
|
T | C | 57 | a0001c0001t0003g0002a0001c0001t0003g0024a0001c0001t0003g0025others(54): Show | 58 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-7157A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210089 | ||||||
chr18:80210167
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.73-7235G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210167 | ||||||
chr18:80210414
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.73-7482A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210414 | ||||||
chr18:80210458
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.73-7526C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210458 | ||||||
chr18:80210509
|
C | T | 66 | a0001c0001t0003g0002a0001c0001t0003g0024a0001c0001t0003g0025others(63): Show | 67 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.73-7577G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210509 | ||||||
chr18:80210510
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | NA18957.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.73-7578C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210510 | ||||||
chr18:80210594
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-7662A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210594 | ||||||
chr18:80210651
|
A | G | 1 | a0001c0002t0001g0355 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.73-7719T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210651 | ||||||
chr18:80210720
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-7788G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210720 | ||||||
chr18:80210807
|
A | T | 14 | a0001c0001t0007g0178a0001c0001t0007g0180a0001c0001t0008g0080others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-7875T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210807 | ||||||
chr18:80210899
|
A | G | 18 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0173others(15): Show | 19 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.73-7967T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210899 | ||||||
chr18:80210912
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.73-7980G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210912 | ||||||
chr18:80210913
|
G | A | 63 | a0001c0001t0002g0003a0001c0001t0003g0020a0001c0001t0003g0037others(60): Show | 66 | HG00323.hp2 HG00438.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.73-7981C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80210913 | ||||||
chr18:80211011
|
T | C | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-8079A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211011 | ||||||
chr18:80211057
|
G | A | 14 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0182others(11): Show | 14 | HG01074.hp1 HG01106.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-8125C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211057 | ||||||
chr18:80211277
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.73-8345A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211277 | ||||||
chr18:80211320
|
T | C | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-8388A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211320 | ||||||
chr18:80211402
|
G | C | 260 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(257): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.73-8470C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211402 | ||||||
chr18:80211420
|
G | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-8488C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211420 | ||||||
chr18:80211467
|
G | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-8535C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211467 | ||||||
chr18:80211579
|
G | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-8647C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211579 | ||||||
chr18:80211679
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.73-8747A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211679 | ||||||
chr18:80211700
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0118 | 2 | HG02015.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.73-8768T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211700 | ||||||
chr18:80211734
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.73-8802C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211734 | ||||||
chr18:80211843
|
T | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(198): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.73-8911A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211843 | ||||||
chr18:80211878
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-8946A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211878 | ||||||
chr18:80211932
|
G | T | 201 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(198): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.73-9000C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211932 | ||||||
chr18:80211946
|
CA | C | 57 | a0001c0001t0003g0002a0001c0001t0003g0024a0001c0001t0003g0025others(54): Show | 58 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-9015delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211946 | ||||||
chr18:80211983
|
G | A | 2 | a0001c0001t0005g0250a0001c0001t0021g0220 | 2 | HG00642.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.73-9051C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80211983 | ||||||
chr18:80212312
|
C | G | 1 | a0001c0001t0032g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.73-9380G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212312 | ||||||
chr18:80212312
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-9380G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212312 | ||||||
chr18:80212607
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-9675G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212607 | ||||||
chr18:80212635
|
C | G | 1 | a0001c0008t0006g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.73-9703G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212635 | ||||||
chr18:80212656
|
C | A | 1 | a0001c0002t0006g0351 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-9724G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212656 | ||||||
chr18:80212657
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73-9725C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212657 | ||||||
chr18:80212681
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.73-9749G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212681 | ||||||
chr18:80212721
|
T | G | 45 | a0001c0001t0003g0020a0001c0001t0003g0055a0001c0001t0003g0057others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.73-9789A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212721 | ||||||
chr18:80212803
|
T | C | 1 | a0001c0002t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.73-9871A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212803 | ||||||
chr18:80212810
|
G | A | 2 | a0001c0002t0006g0350a0001c0002t0006g0351 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.73-9878C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212810 | ||||||
chr18:80212872
|
G | A | 14 | a0001c0001t0003g0025a0001c0001t0003g0059a0001c0001t0003g0068others(11): Show | 14 | HG01243.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-9940C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212872 | ||||||
chr18:80212884
|
C | CA | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-9953dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212884 | ||||||
chr18:80212896
|
A | T | 41 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(38): Show | 41 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.73-9964T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212896 | ||||||
chr18:80212898
|
T | C | 4 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(1): Show | 4 | HG02056.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-9966A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80212898 | ||||||
chr18:80213398
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.73-10466G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213398 | ||||||
chr18:80213411
|
G | A | 1 | a0001c0002t0001g0307 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.73-10479C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213411 | ||||||
chr18:80213464
|
A | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-10532T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213464 | ||||||
chr18:80213681
|
G | A | 1 | a0001c0001t0014g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.73-10749C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213681 | ||||||
chr18:80213715
|
C | G | 2 | a0001c0001t0002g0136a0001c0001t0002g0146 | 2 | NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.73-10783G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213715 | ||||||
chr18:80213763
|
C | A | 8 | a0001c0002t0006g0014a0001c0002t0006g0078a0001c0002t0006g0278others(5): Show | 8 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-10831G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213763 | ||||||
chr18:80213868
|
G | T | 1 | a0001c0001t0007g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.73-10936C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213868 | ||||||
chr18:80213873
|
G | A | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-10941C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213873 | ||||||
chr18:80213946
|
C | CA | 260 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(257): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.73-11015dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213946 | ||||||
chr18:80213946
|
C | CAA | 25 | a0001c0001t0003g0024a0001c0001t0003g0043a0001c0001t0003g0044others(22): Show | 25 | HG01069.hp2 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.73-11016_73-11015d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80213946 | ||||||
chr18:80214017
|
C | T | 2 | a0001c0001t0004g0198a0001c0001t0004g0205 | 2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.73-11085G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214017 | ||||||
chr18:80214056
|
T | C | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.73-11124A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214056 | ||||||
chr18:80214111
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.73-11179T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214111 | ||||||
chr18:80214167
|
A | G | 1 | a0001c0001t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.73-11235T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214167 | ||||||
chr18:80214183
|
C | T | 10 | a0001c0001t0005g0223a0001c0001t0005g0224a0001c0001t0005g0238others(7): Show | 10 | HG00140.hp2 HG00735.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-11251G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214183 | ||||||
chr18:80214224
|
G | A | 1 | a0001c0001t0002g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73-11292C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214224 | ||||||
chr18:80214310
|
C | A | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.73-11378G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214310 | ||||||
chr18:80214456
|
A | G | 41 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(38): Show | 41 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.73-11524T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214456 | ||||||
chr18:80214520
|
A | T | 1 | a0001c0002t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.73-11588T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214520 | ||||||
chr18:80214570
|
C | T | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.73-11638G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214570 | ||||||
chr18:80214800
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-11868T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214800 | ||||||
chr18:80214930
|
A | G | 1 | a0001c0001t0008g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-11998T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80214930 | ||||||
chr18:80215007
|
T | C | 1 | a0001c0001t0004g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-12075A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215007 | ||||||
chr18:80215026
|
TA | T | 267 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(264): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.73-12095delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215026 | ||||||
chr18:80215028
|
A | T | 1 | a0001c0001t0004g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-12096T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215028 | ||||||
chr18:80215286
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-12354T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215286 | ||||||
chr18:80215296
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.73-12364A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215296 | ||||||
chr18:80215398
|
T | A | 2 | a0001c0001t0007g0178a0001c0001t0007g0180 | 2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.73-12466A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215398 | ||||||
chr18:80215445
|
G | A | 6 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0026g0084others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-12513C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215445 | ||||||
chr18:80215463
|
T | C | 1 | a0001c0002t0006g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.73-12531A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215463 | ||||||
chr18:80215518
|
C | T | 2 | a0001c0002t0011g0010a0001c0002t0011g0370 | 3 | HG01891.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.73-12586G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215518 | ||||||
chr18:80215519
|
G | A | 2 | a0001c0001t0016g0095a0001c0001t0016g0096 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.73-12587C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215519 | ||||||
chr18:80215574
|
T | G | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-12642A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215574 | ||||||
chr18:80215671
|
C | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0036a0001c0001t0003g0063others(1): Show | 4 | HG01952.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-12739G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215671 | ||||||
chr18:80215672
|
G | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-12740C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215672 | ||||||
chr18:80215700
|
A | G | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-12768T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215700 | ||||||
chr18:80215819
|
G | T | 59 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(56): Show | 60 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-12887C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215819 | ||||||
chr18:80215845
|
C | A | 1 | a0001c0002t0001g0310 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.73-12913G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215845 | ||||||
chr18:80215851
|
G | C | 1 | a0001c0001t0003g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.73-12919C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215851 | ||||||
chr18:80215995
|
A | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(114): Show | 124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.73-13063T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80215995 | ||||||
chr18:80216241
|
A | G | 1 | a0001c0001t0008g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-13309T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216241 | ||||||
chr18:80216466
|
A | G | 6 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-13534T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216466 | ||||||
chr18:80216585
|
C | T | 1 | a0001c0001t0026g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-13653G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216585 | ||||||
chr18:80216634
|
A | G | 1 | a0001c0001t0012g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-13702T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216634 | ||||||
chr18:80216719
|
T | G | 2 | a0001c0003t0008g0082a0001c0003t0008g0083 | 2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73-13787A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216719 | ||||||
chr18:80216780
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-13848G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216780 | ||||||
chr18:80216936
|
G | C | 1 | a0001c0001t0007g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.73-14004C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80216936 | ||||||
chr18:80217100
|
C | A | 274 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(271): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.73-14168G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217100 | ||||||
chr18:80217134
|
G | A | 4 | a0001c0001t0010g0087a0001c0001t0010g0089a0001c0001t0010g0090others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-14202C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217134 | ||||||
chr18:80217405
|
T | C | 1 | a0001c0002t0001g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.73-14473A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217405 | ||||||
chr18:80217462
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-14530C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217462 | ||||||
chr18:80217578
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73-14646G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217578 | ||||||
chr18:80217588
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.73-14656G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217588 | ||||||
chr18:80217647
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-14715T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217647 | ||||||
chr18:80217829
|
C | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-14897G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217829 | ||||||
chr18:80217851
|
G | GA | 41 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(38): Show | 42 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.73-14920dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217851 | ||||||
chr18:80217899
|
A | G | 74 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(71): Show | 75 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.73-14967T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80217899 | ||||||
chr18:80218201
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-15269G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218201 | ||||||
chr18:80218257
|
T | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(111): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.73-15325A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218257 | ||||||
chr18:80218349
|
C | T | 1 | a0001c0001t0002g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73-15417G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218349 | ||||||
chr18:80218541
|
C | A | 2 | a0001c0001t0008g0080a0001c0001t0008g0085 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.73-15609G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218541 | ||||||
chr18:80218569
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.73-15637G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218569 | ||||||
chr18:80218617
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.73-15685C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218617 | ||||||
chr18:80218912
|
C | T | 1 | a0001c0002t0029g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.73-15980G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218912 | ||||||
chr18:80218944
|
G | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-16012C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80218944 | ||||||
chr18:80219073
|
C | G | 271 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.73-16141G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219073 | ||||||
chr18:80219143
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-16211G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219143 | ||||||
chr18:80219169
|
C | A | 1 | a0001c0002t0006g0270 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.73-16237G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219169 | ||||||
chr18:80219202
|
G | C | 1 | a0001c0001t0005g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.73-16270C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219202 | ||||||
chr18:80219203
|
G | GGTTT | 130 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(127): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.73-16275_73-16272d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219203 | ||||||
chr18:80219203
|
G | GGTTTGTT others(1): Show |
80 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(77): Show | 86 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.73-16279_73-16272d others(10): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219203 | ||||||
chr18:80219205
|
T | TTTGC | 42 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(39): Show | 42 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.73-16274_73-16273i others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219205 | ||||||
chr18:80219270
|
G | A | 1 | a0001c0001t0020g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-16338C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219270 | ||||||
chr18:80219369
|
A | C | 53 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(50): Show | 53 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.73-16437T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219369 | ||||||
chr18:80219401
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-16469T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219401 | ||||||
chr18:80219502
|
G | A | 4 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(1): Show | 4 | HG02056.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-16570C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219502 | ||||||
chr18:80219516
|
T | TC | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-16585dupG | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219516 | ||||||
chr18:80219567
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-16635A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219567 | ||||||
chr18:80219572
|
C | G | 1 | a0001c0004t0004g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-16640G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219572 | ||||||
chr18:80219631
|
T | C | 1 | a0001c0001t0004g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.73-16699A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219631 | ||||||
chr18:80219732
|
C | T | 1 | a0001c0001t0012g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-16800G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219732 | ||||||
chr18:80219788
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.73-16856G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219788 | ||||||
chr18:80219917
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73-16985G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219917 | ||||||
chr18:80219993
|
T | C | 2 | a0001c0002t0006g0273a0001c0002t0006g0274 | 2 | NA18963.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.73-17061A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80219993 | ||||||
chr18:80220016
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.73-17084A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220016 | ||||||
chr18:80220018
|
C | T | 3 | a0001c0001t0007g0104a0001c0001t0007g0105a0001c0001t0007g0106 | 3 | HG01074.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.73-17086G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220018 | ||||||
chr18:80220023
|
A | T | 1 | a0001c0001t0002g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.73-17091T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220023 | ||||||
chr18:80220113
|
G | A | 1 | a0001c0001t0021g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.73-17181C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220113 | ||||||
chr18:80220228
|
G | C | 60 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(57): Show | 61 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.73-17296C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220228 | ||||||
chr18:80220449
|
A | C | 1 | a0001c0001t0008g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.73-17517T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220449 | ||||||
chr18:80220458
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.73-17526A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220458 | ||||||
chr18:80220464
|
A | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-17532T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220464 | ||||||
chr18:80220496
|
C | T | 269 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(266): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.73-17564G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220496 | ||||||
chr18:80220848
|
C | A | 1 | a0001c0001t0005g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.73-17916G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80220848 | ||||||
chr18:80221236
|
A | G | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-18304T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221236 | ||||||
chr18:80221389
|
T | A | 1 | a0001c0001t0007g0106 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.73-18457A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221389 | ||||||
chr18:80221504
|
T | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.73-18572A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221504 | ||||||
chr18:80221607
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0184 | 2 | HG00673.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.73-18675C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221607 | ||||||
chr18:80221686
|
C | T | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.73-18754G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221686 | ||||||
chr18:80221739
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-18807C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221739 | ||||||
chr18:80221769
|
G | A | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-18837C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221769 | ||||||
chr18:80221858
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.73-18926G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221858 | ||||||
chr18:80221863
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-18931A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221863 | ||||||
chr18:80221882
|
T | A | 1 | a0001c0002t0001g0264 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.73-18950A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80221882 | ||||||
chr18:80222073
|
A | C | 1 | a0001c0001t0005g0335 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.73-19141T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222073 | ||||||
chr18:80222181
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.73-19249G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222181 | ||||||
chr18:80222234
|
G | A | 5 | a0001c0001t0010g0086a0001c0001t0010g0087a0001c0001t0010g0089others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-19302C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222234 | ||||||
chr18:80222273
|
A | C | 1 | a0001c0008t0006g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.73-19341T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222273 | ||||||
chr18:80222275
|
A | T | 1 | a0001c0001t0007g0021 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-19343T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222275 | ||||||
chr18:80222286
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-19354G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222286 | ||||||
chr18:80222309
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-19377C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222309 | ||||||
chr18:80222342
|
G | A | 3 | a0001c0001t0007g0104a0001c0001t0007g0105a0001c0001t0007g0106 | 3 | HG01074.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.73-19410C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222342 | ||||||
chr18:80222482
|
T | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0079 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.73-19550A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222482 | ||||||
chr18:80222542
|
G | A | 1 | a0001c0002t0009g0322 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.73-19610C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222542 | ||||||
chr18:80222583
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.73-19651G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222583 | ||||||
chr18:80222608
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-19676G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222608 | ||||||
chr18:80222616
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0027g0368 | 2 | HG02109.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.73-19684G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222616 | ||||||
chr18:80222629
|
C | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-19697G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222629 | ||||||
chr18:80222654
|
T | C | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-19722A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222654 | ||||||
chr18:80222666
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.73-19734A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222666 | ||||||
chr18:80222823
|
G | A | 1 | a0001c0002t0001g0318 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.73-19891C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80222823 | ||||||
chr18:80223029
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20097G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223029 | ||||||
chr18:80223250
|
GA | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20319delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223250 | ||||||
chr18:80223349
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20417T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223349 | ||||||
chr18:80223363
|
G | C | 1 | a0001c0001t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73-20431C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223363 | ||||||
chr18:80223381
|
T | A | 60 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(57): Show | 61 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.73-20449A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223381 | ||||||
chr18:80223415
|
T | C | 1 | a0001c0002t0009g0319 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.73-20483A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223415 | ||||||
chr18:80223465
|
T | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20533A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223465 | ||||||
chr18:80223477
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20545G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223477 | ||||||
chr18:80223496
|
T | C | 1 | a0001c0002t0001g0347 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.73-20564A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223496 | ||||||
chr18:80223593
|
T | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-20661A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223593 | ||||||
chr18:80223599
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-20667A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223599 | ||||||
chr18:80223751
|
C | A | 1 | a0001c0001t0025g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73-20819G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223751 | ||||||
chr18:80223777
|
T | A | 3 | a0001c0001t0002g0114a0001c0001t0002g0143a0001c0001t0002g0161 | 3 | NA18612.hp1 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.73-20845A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223777 | ||||||
chr18:80223941
|
C | T | 41 | a0001c0001t0004g0214a0001c0001t0005g0005a0001c0001t0005g0223others(38): Show | 42 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.73-21009G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223941 | ||||||
chr18:80223959
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-21027A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80223959 | ||||||
chr18:80224220
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0158 | 2 | HG01358.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.73-21288G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224220 | ||||||
chr18:80224224
|
T | C | 115 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.73-21292A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224224 | ||||||
chr18:80224345
|
G | A | 272 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(269): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.73-21413C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224345 | ||||||
chr18:80224359
|
G | A | 1 | a0001c0002t0001g0320 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73-21427C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224359 | ||||||
chr18:80224394
|
C | T | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-21462G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224394 | ||||||
chr18:80224487
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.73-21555C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224487 | ||||||
chr18:80224572
|
G | A | 1 | a0001c0001t0005g0235 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.73-21640C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224572 | ||||||
chr18:80224573
|
T | C | 2 | a0001c0001t0004g0214a0001c0002t0001g0328 | 2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.73-21641A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224573 | ||||||
chr18:80224591
|
T | G | 2 | a0001c0001t0002g0188a0001c0001t0004g0194 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.73-21659A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224591 | ||||||
chr18:80224592
|
A | C | 1 | a0001c0001t0003g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.73-21660T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224592 | ||||||
chr18:80224607
|
A | G | 2 | a0001c0001t0002g0144a0001c0001t0003g0047 | 2 | HG01975.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.73-21675T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224607 | ||||||
chr18:80224614
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.73-21682C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224614 | ||||||
chr18:80224651
|
A | T | 4 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0050others(1): Show | 4 | HG02630.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-21719T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224651 | ||||||
chr18:80224663
|
C | T | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.73-21731G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224663 | ||||||
chr18:80224674
|
C | T | 1 | a0001c0001t0007g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.73-21742G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224674 | ||||||
chr18:80224675
|
A | G | 3 | a0001c0001t0007g0145a0001c0001t0014g0030a0001c0001t0021g0220 | 3 | HG00642.hp1 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.73-21743T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224675 | ||||||
chr18:80224707
|
C | T | 1 | a0001c0002t0013g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-21775G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224707 | ||||||
chr18:80224833
|
T | C | 2 | a0001c0002t0009g0321a0001c0002t0009g0322 | 2 | NA18973.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.73-21901A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224833 | ||||||
chr18:80224846
|
C | CA | 110 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.73-21915dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224846 | ||||||
chr18:80224963
|
C | A | 1 | a0001c0001t0008g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.73-22031G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80224963 | ||||||
chr18:80225019
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(109): Show | 118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.73-22087A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80225019 | ||||||
chr18:80225110
|
C | G | 1 | a0001c0002t0001g0280 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.72+22167G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80225110 | ||||||
chr18:80225144
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.72+22133G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80225144 | ||||||
chr18:80225416
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+21861G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80225416 | ||||||
chr18:80225917
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.72+21360C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80225917 | ||||||
chr18:80226012
|
A | C | 2 | a0001c0001t0002g0101a0001c0002t0002g0102 | 2 | NA19076.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.72+21265T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226012 | ||||||
chr18:80226054
|
G | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.72+21223C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226054 | ||||||
chr18:80226151
|
G | GT | 14 | a0001c0001t0002g0003a0001c0001t0002g0101a0001c0001t0002g0108others(11): Show | 15 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+21125dupA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
G | GTT | 6 | a0001c0001t0002g0107a0001c0001t0002g0115a0001c0001t0002g0117others(3): Show | 6 | HG00735.hp1 HG01106.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+21124_72+21125d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GT | G | 28 | a0001c0001t0002g0004a0001c0001t0002g0094a0001c0001t0002g0099others(25): Show | 29 | HG00140.hp1 HG00423.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.72+21125delA | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTT | G | 23 | a0001c0001t0002g0097a0001c0001t0002g0100a0001c0001t0002g0146others(20): Show | 24 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.72+21124_72+21125d others(4): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTT | G | 10 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(7): Show | 10 | HG01358.hp2 HG01978.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+21123_72+21125d others(5): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTT | G | 49 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(46): Show | 50 | HG01192.hp1 HG01243.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+21122_72+21125d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTTT | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(120): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.72+21121_72+21125d others(7): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTTTT | G | 88 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(85): Show | 91 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.72+21120_72+21125d others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0002g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.72+21116_72+21125d others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+21115_72+21125d others(13): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226151
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0002g0159 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.72+21110_72+21125d others(18): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226151 | ||||||
chr18:80226161
|
T | G | 2 | a0001c0001t0003g0002a0001c0001t0003g0040 | 3 | NA18967.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.72+21116A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226161 | ||||||
chr18:80226162
|
T | G | 7 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0038others(4): Show | 7 | HG01978.hp2 HG02132.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+21115A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226162 | ||||||
chr18:80226163
|
T | G | 48 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(45): Show | 49 | HG01192.hp1 HG01243.hp2 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.72+21114A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226163 | ||||||
chr18:80226164
|
T | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(119): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.72+21113A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226164 | ||||||
chr18:80226165
|
T | G | 87 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(84): Show | 90 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.72+21112A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226165 | ||||||
chr18:80226167
|
T | G | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+21110A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226167 | ||||||
chr18:80226170
|
T | G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+21107A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226170 | ||||||
chr18:80226171
|
T | G | 2 | a0001c0001t0003g0025a0001c0002t0001g0323 | 2 | HG00099.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.72+21106A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226171 | ||||||
chr18:80226212
|
G | A | 199 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.72+21065C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226212 | ||||||
chr18:80226233
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+21044A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226233 | ||||||
chr18:80226247
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(106): Show | 114 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.72+21030G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226247 | ||||||
chr18:80226397
|
C | T | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72+20880G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226397 | ||||||
chr18:80226445
|
A | G | 1 | a0001c0001t0004g0363 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.72+20832T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226445 | ||||||
chr18:80226446
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+20831G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226446 | ||||||
chr18:80226462
|
C | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+20815G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226462 | ||||||
chr18:80226622
|
C | A | 1 | a0001c0001t0003g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.72+20655G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226622 | ||||||
chr18:80226721
|
T | C | 273 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(270): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.72+20556A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226721 | ||||||
chr18:80226834
|
A | T | 47 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(44): Show | 49 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.72+20443T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80226834 | ||||||
chr18:80227088
|
T | C | 1 | a0001c0002t0009g0215 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.72+20189A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227088 | ||||||
chr18:80227412
|
T | C | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.72+19865A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227412 | ||||||
chr18:80227577
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.72+19700T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227577 | ||||||
chr18:80227749
|
C | G | 1 | a0001c0001t0003g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72+19528G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227749 | ||||||
chr18:80227767
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0005g0236 | 2 | HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.72+19510G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227767 | ||||||
chr18:80227813
|
C | T | 2 | a0001c0001t0005g0234a0001c0001t0005g0235 | 2 | HG01256.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.72+19464G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227813 | ||||||
chr18:80227857
|
C | T | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.72+19420G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227857 | ||||||
chr18:80227859
|
T | C | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.72+19418A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227859 | ||||||
chr18:80227874
|
G | C | 1 | a0001c0002t0003g0367 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.72+19403C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227874 | ||||||
chr18:80227876
|
C | G | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.72+19401G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227876 | ||||||
chr18:80227878
|
T | G | 270 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(267): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.72+19399A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227878 | ||||||
chr18:80227947
|
C | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+19330G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227947 | ||||||
chr18:80227989
|
A | G | 1 | a0001c0001t0030g0266 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.72+19288T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80227989 | ||||||
chr18:80228015
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+19262A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228015 | ||||||
chr18:80228034
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+19243C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228034 | ||||||
chr18:80228231
|
G | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.72+19046C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228231 | ||||||
chr18:80228247
|
G | A | 24 | a0001c0001t0003g0002a0001c0001t0003g0026a0001c0001t0003g0027others(21): Show | 25 | HG00323.hp1 HG01192.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.72+19030C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228247 | ||||||
chr18:80228281
|
TGGGGAGG others(3): Show |
T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18986_72+18995d others(12): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228281 | ||||||
chr18:80228354
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.72+18923T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228354 | ||||||
chr18:80228382
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18895A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228382 | ||||||
chr18:80228406
|
C | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+18871G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228406 | ||||||
chr18:80228411
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.72+18866T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228411 | ||||||
chr18:80228412
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18865A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228412 | ||||||
chr18:80228460
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18817T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228460 | ||||||
chr18:80228494
|
C | T | 47 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(44): Show | 49 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.72+18783G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228494 | ||||||
chr18:80228568
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18709G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228568 | ||||||
chr18:80228664
|
C | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18613G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228664 | ||||||
chr18:80228730
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.72+18547T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228730 | ||||||
chr18:80228838
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18439A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228838 | ||||||
chr18:80228962
|
G | A | 1 | a0001c0002t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+18315C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80228962 | ||||||
chr18:80229041
|
C | G | 11 | a0001c0001t0002g0327a0001c0001t0004g0259a0001c0001t0006g0258others(8): Show | 11 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+18236G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229041 | ||||||
chr18:80229249
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+18028A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229249 | ||||||
chr18:80229278
|
C | A | 1 | a0001c0002t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+17999G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229278 | ||||||
chr18:80229346
|
G | T | 42 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+17931C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229346 | ||||||
chr18:80229349
|
A | T | 10 | a0001c0002t0001g0257a0001c0002t0001g0261a0001c0002t0001g0262others(7): Show | 10 | HG00408.hp1 HG00621.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+17928T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229349 | ||||||
chr18:80229383
|
A | G | 1 | a0001c0001t0002g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+17894T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229383 | ||||||
chr18:80229471
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.72+17806G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80229471 | ||||||
chr18:80230070
|
A | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+17207T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230070 | ||||||
chr18:80230152
|
T | C | 1 | a0001c0001t0021g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.72+17125A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230152 | ||||||
chr18:80230205
|
G | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0036a0001c0001t0003g0063others(1): Show | 4 | HG01952.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+17072C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230205 | ||||||
chr18:80230214
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+17063G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230214 | ||||||
chr18:80230333
|
G | C | 41 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(38): Show | 42 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.72+16944C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230333 | ||||||
chr18:80230358
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+16919G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230358 | ||||||
chr18:80230363
|
G | A | 1 | a0001c0002t0001g0326 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.72+16914C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230363 | ||||||
chr18:80230443
|
G | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(41): Show | 45 | HG00323.hp1 HG01192.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.72+16834C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230443 | ||||||
chr18:80230747
|
G | C | 12 | a0001c0001t0008g0029a0001c0001t0008g0080a0001c0001t0008g0085others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+16530C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80230747 | ||||||
chr18:80231688
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+15589A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80231688 | ||||||
chr18:80231967
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72+15310G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80231967 | ||||||
chr18:80232012
|
G | A | 1 | a0001c0002t0029g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.72+15265C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232012 | ||||||
chr18:80232154
|
A | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+15123T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232154 | ||||||
chr18:80232291
|
C | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+14986G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232291 | ||||||
chr18:80232478
|
G | C | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+14799C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232478 | ||||||
chr18:80232482
|
C | G | 1 | a0001c0001t0030g0266 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.72+14795G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232482 | ||||||
chr18:80232564
|
C | G | 49 | a0001c0001t0002g0100a0001c0001t0002g0108a0001c0001t0002g0109others(46): Show | 50 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+14713G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232564 | ||||||
chr18:80232641
|
AACACGTG others(14): Show |
A | 107 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(104): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.72+14615_72+14635d others(23): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232641 | ||||||
chr18:80232921
|
C | T | 1 | a0001c0002t0029g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.72+14356G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80232921 | ||||||
chr18:80233091
|
A | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0033a0001c0001t0003g0034 | 4 | NA18967.hp2 NA18979.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+14186T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233091 | ||||||
chr18:80233116
|
C | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+14161G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233116 | ||||||
chr18:80233116
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.72+14161G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233116 | ||||||
chr18:80233323
|
C | T | 1 | a0001c0002t0006g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+13954G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233323 | ||||||
chr18:80233324
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+13953C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233324 | ||||||
chr18:80233361
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+13916G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233361 | ||||||
chr18:80233518
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.72+13759T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233518 | ||||||
chr18:80233557
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+13720C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233557 | ||||||
chr18:80233591
|
C | T | 1 | a0001c0001t0004g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+13686G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233591 | ||||||
chr18:80233592
|
G | A | 1 | a0001c0002t0001g0324 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.72+13685C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233592 | ||||||
chr18:80233596
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+13681A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233596 | ||||||
chr18:80233644
|
T | C | 74 | a0001c0001t0002g0003a0001c0001t0003g0002a0001c0001t0003g0022others(71): Show | 76 | HG00323.hp1 HG01069.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.72+13633A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233644 | ||||||
chr18:80233969
|
C | T | 3 | a0001c0001t0003g0038a0001c0001t0003g0040a0001c0001t0031g0039 | 3 | NA18999.hp2 NA19054.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.72+13308G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80233969 | ||||||
chr18:80234102
|
G | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(102): Show | 110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.72+13175C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234102 | ||||||
chr18:80234156
|
TTTCA | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+13117_72+13120d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234156 | ||||||
chr18:80234216
|
G | T | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+13061C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234216 | ||||||
chr18:80234340
|
C | T | 1 | a0001c0001t0002g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.72+12937G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234340 | ||||||
chr18:80234414
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72+12863C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234414 | ||||||
chr18:80234510
|
G | C | 1 | a0001c0001t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+12767C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234510 | ||||||
chr18:80234829
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+12448G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234829 | ||||||
chr18:80234894
|
C | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+12383G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234894 | ||||||
chr18:80234937
|
TAGAC | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+12336_72+12339d others(6): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80234937 | ||||||
chr18:80235115
|
A | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+12162T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235115 | ||||||
chr18:80235216
|
A | G | 1 | a0001c0002t0001g0348 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.72+12061T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235216 | ||||||
chr18:80235311
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11966C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235311 | ||||||
chr18:80235351
|
T | C | 48 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(45): Show | 50 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+11926A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235351 | ||||||
chr18:80235376
|
T | G | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+11901A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235376 | ||||||
chr18:80235442
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11835T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235442 | ||||||
chr18:80235534
|
C | T | 1 | a0001c0001t0032g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+11743G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235534 | ||||||
chr18:80235608
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11669C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235608 | ||||||
chr18:80235710
|
G | C | 2 | a0001c0001t0014g0030a0001c0001t0014g0031 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.72+11567C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235710 | ||||||
chr18:80235749
|
A | G | 4 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(1): Show | 5 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+11528T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235749 | ||||||
chr18:80235770
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11507G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235770 | ||||||
chr18:80235867
|
G | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11410C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235867 | ||||||
chr18:80235882
|
C | A | 1 | a0001c0002t0001g0325 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.72+11395G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235882 | ||||||
chr18:80235936
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.72+11341C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235936 | ||||||
chr18:80235964
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+11313G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80235964 | ||||||
chr18:80236120
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11157T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236120 | ||||||
chr18:80236154
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+11123G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236154 | ||||||
chr18:80236160
|
A | G | 1 | a0001c0001t0003g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.72+11117T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236160 | ||||||
chr18:80236242
|
G | A | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+11035C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236242 | ||||||
chr18:80236277
|
A | G | 5 | a0001c0001t0007g0021a0001c0001t0007g0103a0001c0001t0007g0104others(2): Show | 5 | HG01074.hp1 HG01106.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+11000T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236277 | ||||||
chr18:80236304
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.72+10973G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236304 | ||||||
chr18:80236371
|
T | C | 1 | a0001c0001t0002g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.72+10906A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236371 | ||||||
chr18:80236479
|
A | G | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | NA18943.hp2 NA18975.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+10798T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236479 | ||||||
chr18:80236538
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10739C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236538 | ||||||
chr18:80236607
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+10670G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236607 | ||||||
chr18:80236688
|
A | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0033a0001c0001t0003g0034 | 4 | NA18967.hp2 NA18979.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+10589T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236688 | ||||||
chr18:80236766
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10511T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236766 | ||||||
chr18:80236790
|
A | G | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10487T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236790 | ||||||
chr18:80236887
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.72+10390C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236887 | ||||||
chr18:80236920
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10357A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236920 | ||||||
chr18:80236928
|
G | A | 1 | a0001c0002t0001g0326 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.72+10349C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236928 | ||||||
chr18:80236953
|
C | G | 1 | a0001c0008t0006g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.72+10324G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80236953 | ||||||
chr18:80237032
|
G | C | 1 | a0001c0001t0002g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.72+10245C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237032 | ||||||
chr18:80237080
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10197T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237080 | ||||||
chr18:80237137
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.72+10140C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237137 | ||||||
chr18:80237142
|
CA | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10134delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237142 | ||||||
chr18:80237459
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9818T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237459 | ||||||
chr18:80237465
|
A | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9812T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237465 | ||||||
chr18:80237532
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9745T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237532 | ||||||
chr18:80237558
|
C | T | 107 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(104): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.72+9719G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237558 | ||||||
chr18:80237562
|
T | C | 118 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(115): Show | 123 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.72+9715A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237562 | ||||||
chr18:80237704
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9573A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237704 | ||||||
chr18:80237728
|
C | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9549G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237728 | ||||||
chr18:80237823
|
T | C | 66 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(63): Show | 67 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.72+9454A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237823 | ||||||
chr18:80237852
|
T | A | 1 | a0001c0001t0002g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+9425A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237852 | ||||||
chr18:80237893
|
T | C | 66 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(63): Show | 67 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.72+9384A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237893 | ||||||
chr18:80237912
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9365T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237912 | ||||||
chr18:80237922
|
T | C | 1 | a0001c0002t0001g0328 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.72+9355A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237922 | ||||||
chr18:80237981
|
G | A | 1 | a0001c0001t0008g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.72+9296C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80237981 | ||||||
chr18:80238013
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9264A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238013 | ||||||
chr18:80238048
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+9229C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238048 | ||||||
chr18:80238144
|
C | T | 12 | a0001c0001t0004g0194a0001c0001t0008g0080a0001c0001t0008g0085others(9): Show | 12 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+9133G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238144 | ||||||
chr18:80238175
|
G | A | 8 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+9102C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238175 | ||||||
chr18:80238219
|
G | T | 8 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+9058C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238219 | ||||||
chr18:80238380
|
T | C | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+8897A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238380 | ||||||
chr18:80238491
|
C | CA | 45 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(42): Show | 46 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.72+8785dupT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238491 | ||||||
chr18:80238491
|
C | CAA | 7 | a0001c0001t0005g0344a0001c0001t0005g0345a0001c0001t0010g0086others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+8784_72+8785dup others(2): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238491 | ||||||
chr18:80238500
|
A | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+8777T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238500 | ||||||
chr18:80238507
|
T | C | 1 | a0001c0001t0007g0170 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.72+8770A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238507 | ||||||
chr18:80238590
|
G | A | 3 | a0001c0003t0008g0082a0001c0003t0008g0083a0002c0006t0028g0081 | 3 | HG02809.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.72+8687C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238590 | ||||||
chr18:80238660
|
C | T | 5 | a0001c0001t0008g0029a0001c0001t0008g0032a0001c0001t0014g0030others(2): Show | 5 | HG02056.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+8617G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80238660 | ||||||
chr18:80239060
|
G | T | 1 | a0001c0001t0022g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+8217C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239060 | ||||||
chr18:80239119
|
G | A | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+8158C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239119 | ||||||
chr18:80239123
|
C | T | 2 | a0001c0001t0004g0175a0001c0001t0004g0176 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.72+8154G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239123 | ||||||
chr18:80239169
|
A | G | 276 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.72+8108T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239169 | ||||||
chr18:80239256
|
GA | G | 41 | a0001c0001t0005g0005a0001c0001t0005g0223a0001c0001t0005g0224others(38): Show | 42 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.72+8020delT | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239256 | ||||||
chr18:80239308
|
T | C | 115 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(112): Show | 117 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.72+7969A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239308 | ||||||
chr18:80239406
|
G | A | 1 | a0001c0002t0001g0362 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.72+7871C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239406 | ||||||
chr18:80239517
|
T | C | 4 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0167others(1): Show | 4 | NA18971.hp2 NA18991.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+7760A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239517 | ||||||
chr18:80239580
|
G | C | 15 | a0001c0001t0005g0254a0001c0001t0005g0332a0001c0001t0005g0333others(12): Show | 15 | HG00621.hp2 NA18942.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+7697C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239580 | ||||||
chr18:80239649
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.72+7628G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239649 | ||||||
chr18:80239696
|
C | G | 2 | a0001c0001t0005g0332a0001c0001t0005g0333 | 2 | HG00621.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.72+7581G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239696 | ||||||
chr18:80239723
|
T | C | 73 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(70): Show | 74 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.72+7554A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239723 | ||||||
chr18:80239738
|
G | C | 1 | a0001c0002t0002g0168 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.72+7539C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239738 | ||||||
chr18:80239895
|
C | CAAGAAGC others(72): Show |
1 | a0001c0001t0003g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.72+7381_72+7382ins others(79): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80239895 | ||||||
chr18:80240114
|
G | T | 1 | a0001c0001t0003g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.72+7163C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240114 | ||||||
chr18:80240191
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+7086A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240191 | ||||||
chr18:80240251
|
G | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+7026C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240251 | ||||||
chr18:80240326
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+6951C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240326 | ||||||
chr18:80240362
|
T | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0066 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.72+6915A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240362 | ||||||
chr18:80240375
|
C | T | 1 | a0001c0001t0026g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72+6902G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240375 | ||||||
chr18:80240452
|
G | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(103): Show | 111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.72+6825C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240452 | ||||||
chr18:80240457
|
C | A | 63 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(60): Show | 64 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.72+6820G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240457 | ||||||
chr18:80240468
|
C | G | 5 | a0001c0001t0004g0191a0001c0001t0004g0193a0001c0002t0001g0013others(2): Show | 5 | HG00438.hp2 HG03492.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+6809G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240468 | ||||||
chr18:80240492
|
A | G | 61 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(58): Show | 62 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+6785T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240492 | ||||||
chr18:80240613
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.72+6664G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240613 | ||||||
chr18:80240662
|
C | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+6615G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240662 | ||||||
chr18:80240743
|
G | T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+6534C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240743 | ||||||
chr18:80240794
|
G | A | 3 | a0001c0001t0005g0253a0001c0002t0006g0350a0001c0002t0006g0351 | 3 | HG03130.hp2 NA18906.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.72+6483C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240794 | ||||||
chr18:80240937
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+6340A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80240937 | ||||||
chr18:80241058
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.72+6219G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241058 | ||||||
chr18:80241089
|
A | G | 48 | a0001c0001t0003g0020a0001c0001t0003g0077a0001c0001t0003g0366others(45): Show | 50 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+6188T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241089 | ||||||
chr18:80241239
|
T | C | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+6038A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241239 | ||||||
chr18:80241262
|
C | T | 1 | a0001c0001t0017g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+6015G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241262 | ||||||
chr18:80241297
|
C | A | 15 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0025others(12): Show | 15 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+5980G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241297 | ||||||
chr18:80241342
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.72+5935G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241342 | ||||||
chr18:80241406
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.72+5871G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241406 | ||||||
chr18:80241427
|
AGATGGGC others(64): Show |
A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5779_72+5849del others(71): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241427 | ||||||
chr18:80241447
|
T | A | 1 | a0001c0002t0004g0219 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.72+5830A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241447 | ||||||
chr18:80241565
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5712C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241565 | ||||||
chr18:80241635
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.72+5642C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241635 | ||||||
chr18:80241742
|
T | G | 1 | a0001c0002t0006g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+5535A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241742 | ||||||
chr18:80241774
|
T | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5503A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241774 | ||||||
chr18:80241786
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5491T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241786 | ||||||
chr18:80241809
|
A | G | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5468T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241809 | ||||||
chr18:80241825
|
C | T | 1 | a0001c0001t0003g0024 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.72+5452G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241825 | ||||||
chr18:80241852
|
T | G | 1 | a0001c0001t0001g0329 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.72+5425A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241852 | ||||||
chr18:80241912
|
T | C | 1 | a0001c0002t0001g0330 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.72+5365A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241912 | ||||||
chr18:80241920
|
G | A | 1 | a0001c0001t0021g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.72+5357C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80241920 | ||||||
chr18:80242171
|
TTGGGTCC others(1): Show |
T | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5098_72+5105del others(8): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242171 | ||||||
chr18:80242316
|
G | A | 2 | a0001c0001t0007g0169a0001c0001t0007g0170 | 2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.72+4961C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242316 | ||||||
chr18:80242397
|
C | G | 1 | a0001c0001t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+4880G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242397 | ||||||
chr18:80242558
|
C | G | 61 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(58): Show | 62 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+4719G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242558 | ||||||
chr18:80242574
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.72+4703G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242574 | ||||||
chr18:80242595
|
G | A | 11 | a0001c0001t0008g0080a0001c0001t0008g0085a0001c0001t0010g0086others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+4682C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242595 | ||||||
chr18:80242689
|
A | T | 3 | a0001c0003t0008g0082a0001c0003t0008g0083a0002c0006t0028g0081 | 3 | HG02809.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.72+4588T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242689 | ||||||
chr18:80242893
|
A | G | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+4384T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242893 | ||||||
chr18:80242969
|
A | T | 2 | a0001c0001t0004g0259a0001c0001t0006g0258 | 2 | HG00099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.72+4308T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80242969 | ||||||
chr18:80243028
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.72+4249G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80243028 | ||||||
chr18:80243385
|
G | A | 1 | a0001c0002t0001g0331 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.72+3892C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80243385 | ||||||
chr18:80243399
|
C | A | 104 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(101): Show | 109 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.72+3878G>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80243399 | ||||||
chr18:80243704
|
C | T | 2 | a0001c0001t0003g0022a0001c0001t0003g0023 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.72+3573G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80243704 | ||||||
chr18:80243936
|
C | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(256): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.72+3341G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80243936 | ||||||
chr18:80244030
|
C | G | 1 | a0001c0001t0005g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.72+3247G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244030 | ||||||
chr18:80244130
|
C | T | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+3147G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244130 | ||||||
chr18:80244138
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.72+3139A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244138 | ||||||
chr18:80244171
|
C | T | 6 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0174others(3): Show | 6 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3106G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244171 | ||||||
chr18:80244172
|
G | A | 42 | a0001c0001t0004g0221a0001c0001t0004g0222a0001c0001t0005g0005others(39): Show | 43 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+3105C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244172 | ||||||
chr18:80244288
|
A | T | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.72+2989T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244288 | ||||||
chr18:80244356
|
T | C | 273 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(270): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.72+2921A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244356 | ||||||
chr18:80244424
|
C | T | 5 | a0001c0002t0011g0010a0001c0002t0011g0370a0001c0002t0011g0371others(2): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2853G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244424 | ||||||
chr18:80244427
|
G | A | 10 | a0001c0001t0008g0085a0001c0001t0010g0086a0001c0001t0010g0087others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2850C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244427 | ||||||
chr18:80244442
|
T | C | 1 | a0001c0001t0004g0225 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.72+2835A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244442 | ||||||
chr18:80244646
|
T | A | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+2631A>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244646 | ||||||
chr18:80244789
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.72+2488C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244789 | ||||||
chr18:80244847
|
T | C | 238 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0287others(235): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.72+2430A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244847 | ||||||
chr18:80244913
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.72+2364C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80244913 | ||||||
chr18:80245324
|
A | C | 75 | a0001c0001t0003g0366a0001c0001t0004g0001a0001c0001t0004g0187others(72): Show | 79 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.72+1953T>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245324 | ||||||
chr18:80245397
|
A | T | 1 | a0001c0001t0004g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+1880T>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245397 | ||||||
chr18:80245424
|
G | A | 61 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0023others(58): Show | 62 | HG00323.hp1 HG01069.hp2 HG01192.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+1853C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245424 | ||||||
chr18:80245610
|
A | G | 1 | a0001c0002t0001g0346 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.72+1667T>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245610 | ||||||
chr18:80245640
|
T | C | 5 | a0001c0002t0001g0009a0001c0002t0001g0346a0001c0002t0001g0347others(2): Show | 6 | HG00597.hp1 NA18960.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+1637A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245640 | ||||||
chr18:80245690
|
G | A | 271 | a0001c0001t0001g0007a0001c0001t0001g0287a0001c0001t0001g0293others(268): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.72+1587C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80245690 | ||||||
chr18:80246004
|
C | T | 1 | a0001c0001t0019g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72+1273G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246004 | ||||||
chr18:80246026
|
T | C | 65 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(62): Show | 66 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.72+1251A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246026 | ||||||
chr18:80246049
|
G | A | 11 | a0001c0002t0001g0352a0001c0002t0001g0353a0001c0002t0001g0354others(8): Show | 11 | HG00673.hp2 HG01928.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+1228C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246049 | ||||||
chr18:80246143
|
G | A | 1 | a0001c0001t0004g0363 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.72+1134C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246143 | ||||||
chr18:80246165
|
T | C | 196 | a0001c0001t0001g0007a0001c0001t0001g0287a0001c0001t0001g0293others(193): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.72+1112A>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246165 | ||||||
chr18:80246249
|
C | T | 75 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(72): Show | 76 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.72+1028G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246249 | ||||||
chr18:80246258
|
C | G | 1 | a0001c0001t0003g0079 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72+1019G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246258 | ||||||
chr18:80246353
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72+924C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246353 | ||||||
chr18:80246385
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+892C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246385 | ||||||
chr18:80246448
|
C | T | 64 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0022others(61): Show | 65 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.72+829G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246448 | ||||||
chr18:80246462
|
G | C | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+815C>G | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246462 | ||||||
chr18:80246598
|
AGGTGGGG others(38): Show |
A | 1 | a0001c0002t0001g0364 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.72+634_72+678delCC others(43): Show |
PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246598 | ||||||
chr18:80246709
|
G | A | 1 | a0001c0001t0004g0365 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.72+568C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246709 | ||||||
chr18:80246738
|
G | T | 2 | a0001c0002t0002g0015a0001c0002t0002g0016 | 2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.72+539C>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246738 | ||||||
chr18:80246759
|
T | G | 2 | a0001c0001t0003g0366a0001c0002t0003g0367 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+518A>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246759 | ||||||
chr18:80246833
|
C | G | 1 | a0001c0002t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+444G>C | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246833 | ||||||
chr18:80246885
|
C | T | 1 | a0001c0002t0001g0013 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.72+392G>A | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246885 | ||||||
chr18:80246998
|
G | A | 1 | a0001c0001t0027g0368 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+279C>T | PARD6G | ENSG00000178184.16 | transcript | ENST00000353265.8 | protein_coding | 1/2 | chr18 | 80246998 |