geneid | 5311 |
---|---|
ensemblid | ENSG00000118762.8 |
hgncid | 9009 |
symbol | PKD2 |
name | polycystin 2, transient receptor potential cation channel |
refseq_nuc | NM_000297.4 |
refseq_prot | NP_000288.1 |
ensembl_nuc | ENST00000237596.7 |
ensembl_prot | ENSP00000237596.2 |
mane_status | MANE Select |
chr | chr4 |
start | 88007635 |
end | 88077777 |
strand | + |
ver | v1.2 |
region | chr4:88007635-88077777 |
region5000 | chr4:88002635-88082777 |
regionname0 | PKD2_chr4_88007635_88077777 |
regionname5000 | PKD2_chr4_88002635_88082777 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 968 | 244 | 58 | 45 | 114 | 6 | 20 | 97 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002 | 0/0 | 968 | 46 | 0 | 5 | 37 | 2 | 2 | 29 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003 | 0/1 | 968 | 34 | 13 | 12 | 0 | 2 | 6 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0004 | 0/0 | 968 | 8 | 0 | 0 | 7 | 0 | 1 | 4 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005 | 0/0 | 969 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0006 | 0/0 | 968 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0007 | 0/0 | 968 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0008 | 0/0 | 968 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0009 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0010 | 0/0 | 968 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0011 | 0/0 | 968 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2907 | 148 | 48 | 29 | 53 | 4 | 13 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0002 | 0/0 | 2907 | 82 | 0 | 14 | 61 | 2 | 5 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0003 | 0/0 | 2907 | 45 | 0 | 5 | 36 | 2 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0004 | 0/1 | 2907 | 30 | 10 | 11 | 0 | 2 | 6 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0005 | 0/0 | 2907 | 8 | 0 | 0 | 7 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0006 | 0/0 | 2907 | 4 | 4 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0007 | 0/0 | 2907 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0008 | 0/0 | 2910 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0009 | 0/0 | 2907 | 2 | 1 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0010 | 0/0 | 2907 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0011 | 0/0 | 2907 | 2 | 1 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0012 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0013 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0014 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0015 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0016 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0017 | 0/0 | 2907 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0018 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0019 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0020 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0021 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0022 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
c0023 | 0/0 | 2907 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2183 | 192 | 52 | 32 | 84 | 5 | 18 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0002 | 0/0 | 2183 | 69 | 1 | 10 | 50 | 2 | 6 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0003 | 0/0 | 2183 | 39 | 5 | 7 | 23 | 1 | 3 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0004 | 0/1 | 2183 | 24 | 5 | 14 | 0 | 2 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0005 | 0/0 | 2183 | 8 | 7 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0006 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0007 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0008 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0009 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0010 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0011 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0012 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0013 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0014 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
t0015 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2907 | 148 | 48 | 29 | 53 | 4 | 13 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0002 | 0/0 | 2907 | 82 | 0 | 14 | 61 | 2 | 5 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0006 | 0/0 | 2907 | 4 | 4 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0009 | 0/0 | 2907 | 2 | 1 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0010 | 0/0 | 2907 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0012 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0013 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0017 | 0/0 | 2907 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0022 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002c0003 | 0/0 | 2907 | 45 | 0 | 5 | 36 | 2 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002c0019 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0004 | 0/1 | 2907 | 30 | 10 | 11 | 0 | 2 | 6 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0007 | 0/0 | 2907 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0015 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0004c0005 | 0/0 | 2907 | 8 | 0 | 0 | 7 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005c0008 | 0/0 | 2910 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005c0016 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0006c0011 | 0/0 | 2907 | 2 | 1 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0007c0014 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0008c0023 | 0/0 | 2907 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0009c0018 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0010c0020 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0011c0021 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5089 | 125 | 40 | 23 | 45 | 4 | 12 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0002 | 0/0 | 5089 | 3 | 0 | 3 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0003 | 0/0 | 5089 | 5 | 0 | 0 | 5 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0004 | 0/0 | 5089 | 5 | 2 | 3 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0006 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0007 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0008 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0009 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0010 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0011 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0012 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0013 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0014 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0001t0015 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0002t0001 | 0/0 | 5089 | 19 | 0 | 8 | 11 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0002t0002 | 0/0 | 5089 | 63 | 0 | 6 | 50 | 2 | 5 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0006t0001 | 0/0 | 5089 | 4 | 4 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0009t0001 | 0/0 | 5089 | 2 | 1 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0010t0004 | 0/0 | 5089 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0012t0003 | 0/0 | 5089 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0013t0003 | 0/0 | 5089 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0017t0002 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0001c0022t0001 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002c0003t0001 | 0/0 | 5089 | 19 | 0 | 0 | 18 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002c0003t0003 | 0/0 | 5089 | 26 | 0 | 5 | 18 | 1 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0002c0019t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0004t0001 | 0/0 | 5089 | 8 | 3 | 1 | 0 | 0 | 4 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0004t0004 | 0/1 | 5089 | 14 | 0 | 9 | 0 | 2 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0004t0005 | 0/0 | 5089 | 8 | 7 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0007t0004 | 0/0 | 5089 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0003c0015t0003 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0004c0005t0001 | 0/0 | 5089 | 8 | 0 | 0 | 7 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005c0008t0001 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005c0008t0003 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0005c0016t0001 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0006c0011t0002 | 0/0 | 5089 | 2 | 1 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0007c0014t0003 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0008c0023t0003 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0009c0018t0001 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0010c0020t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
a0011c0021t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | copy fasta | chr4 | 88002635 | 88082777 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0014g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0001t0015g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0006t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0006t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0006t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0009t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0009t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0010t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0010t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0012t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0012t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0013t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0013t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0017t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0001c0022t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0002c0019t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0007t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0007t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0007t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0003c0015t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0004c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0005c0008t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0005c0008t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0005c0016t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0006c0011t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0006c0011t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0007c0014t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0008c0023t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0009c0018t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0010c0020t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
a0011c0021t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0137 | EUR | FIN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00323 | hp2 | a0003 | c0004 | t0004 | g0208 | EUR | FIN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00558 | hp2 | a0004 | c0005 | t0001 | g0252 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00609 | hp1 | a0002 | c0003 | t0001 | g0060 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00642 | hp1 | a0003 | c0004 | t0004 | g0206 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01099 | hp2 | a0003 | c0004 | t0004 | g0200 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01109 | hp1 | a0003 | c0004 | t0005 | g0026 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01167 | hp1 | a0001 | c0010 | t0004 | g0100 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01167 | hp2 | a0003 | c0015 | t0003 | g0024 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01175 | hp1 | a0003 | c0004 | t0004 | g0199 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01192 | hp1 | a0003 | c0004 | t0004 | g0204 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01192 | hp2 | a0001 | c0010 | t0004 | g0101 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01243 | hp2 | a0003 | c0004 | t0001 | g0030 | AMR | PUR | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01255 | hp1 | a0007 | c0014 | t0003 | g0198 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01256 | hp2 | a0003 | c0004 | t0004 | g0216 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01257 | hp1 | a0003 | c0004 | t0004 | g0017 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01258 | hp2 | a0003 | c0004 | t0004 | g0205 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0178 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0241 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01516 | hp1 | a0002 | c0003 | t0003 | g0068 | EUR | IBS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01884 | hp2 | a0001 | c0006 | t0001 | g0018 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01891 | hp1 | a0003 | c0004 | t0001 | g0209 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01891 | hp2 | a0001 | c0009 | t0001 | g0229 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01928 | hp1 | a0002 | c0003 | t0003 | g0036 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01952 | hp2 | a0002 | c0003 | t0003 | g0038 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01978 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01981 | hp2 | a0006 | c0011 | t0002 | g0095 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01993 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02004 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02004 | hp2 | a0003 | c0004 | t0004 | g0017 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02015 | hp1 | a0002 | c0003 | t0003 | g0071 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02027 | hp2 | a0002 | c0003 | t0003 | g0056 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02040 | hp2 | a0004 | c0005 | t0001 | g0245 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02055 | hp2 | a0003 | c0007 | t0004 | g0020 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02129 | hp1 | a0004 | c0005 | t0001 | g0299 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02145 | hp2 | a0001 | c0022 | t0001 | g0304 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02155 | hp1 | a0002 | c0003 | t0003 | g0073 | EAS | CDX | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | CDX | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02572 | hp1 | a0005 | c0008 | t0003 | g0225 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02572 | hp2 | a0001 | c0012 | t0003 | g0111 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02615 | hp1 | a0001 | c0012 | t0003 | g0142 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02723 | hp2 | a0006 | c0011 | t0002 | g0094 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02738 | hp1 | a0001 | c0009 | t0001 | g0287 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0219 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02809 | hp2 | a0003 | c0004 | t0005 | g0027 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02818 | hp2 | a0003 | c0004 | t0005 | g0019 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02895 | hp2 | a0003 | c0004 | t0005 | g0032 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02896 | hp1 | a0005 | c0016 | t0001 | g0226 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02896 | hp2 | a0003 | c0007 | t0004 | g0021 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02897 | hp1 | a0003 | c0007 | t0004 | g0022 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02897 | hp2 | a0003 | c0004 | t0005 | g0025 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02965 | hp2 | a0003 | c0004 | t0005 | g0029 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0143 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03195 | hp2 | a0001 | c0006 | t0001 | g0218 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03453 | hp2 | a0003 | c0004 | t0005 | g0028 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03490 | hp1 | a0003 | c0004 | t0001 | g0211 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0177 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0222 | AFR | ESN | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03669 | hp2 | a0003 | c0004 | t0001 | g0212 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03704 | hp1 | a0001 | c0017 | t0002 | g0134 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03704 | hp2 | a0003 | c0004 | t0004 | g0213 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03710 | hp1 | a0003 | c0004 | t0001 | g0215 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03831 | hp1 | a0008 | c0023 | t0003 | g0302 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03927 | hp1 | a0002 | c0003 | t0003 | g0072 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04184 | hp1 | a0004 | c0005 | t0001 | g0043 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04184 | hp2 | a0003 | c0004 | t0004 | g0202 | SAS | BEB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | STU | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG04228 | hp2 | a0003 | c0004 | t0001 | g0210 | SAS | STU | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18612 | hp1 | a0002 | c0003 | t0003 | g0058 | EAS | CHB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18747 | hp1 | a0002 | c0003 | t0003 | g0079 | EAS | CHB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | CHB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18906 | hp1 | a0001 | c0006 | t0001 | g0217 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18946 | hp2 | a0004 | c0005 | t0001 | g0278 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18950 | hp2 | a0004 | c0005 | t0001 | g0297 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18952 | hp2 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18954 | hp2 | a0002 | c0003 | t0003 | g0311 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18956 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18959 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18960 | hp2 | a0010 | c0020 | t0001 | g0054 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18966 | hp1 | a0002 | c0003 | t0003 | g0063 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18969 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18971 | hp2 | a0001 | c0001 | t0014 | g0274 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18972 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18974 | hp1 | a0002 | c0003 | t0003 | g0040 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18977 | hp1 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18979 | hp2 | a0002 | c0003 | t0003 | g0067 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18982 | hp2 | a0002 | c0003 | t0003 | g0081 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18983 | hp2 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18986 | hp2 | a0011 | c0021 | t0001 | g0059 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19000 | hp1 | a0002 | c0003 | t0003 | g0074 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19030 | hp1 | a0003 | c0004 | t0001 | g0203 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19043 | hp2 | a0001 | c0013 | t0003 | g0033 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19057 | hp1 | a0004 | c0005 | t0001 | g0262 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19062 | hp2 | a0004 | c0005 | t0001 | g0246 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19065 | hp1 | a0002 | c0003 | t0003 | g0042 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19081 | hp1 | a0001 | c0001 | t0011 | g0243 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19085 | hp1 | a0001 | c0001 | t0013 | g0264 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19086 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19087 | hp1 | a0002 | c0019 | t0001 | g0080 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19240 | hp1 | a0001 | c0013 | t0003 | g0034 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0179 | EUR | TSI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0065 | EUR | TSI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20805 | hp2 | a0003 | c0004 | t0004 | g0214 | EUR | TSI | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | GIH | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20905 | hp2 | a0002 | c0003 | t0003 | g0070 | SAS | GIH | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG01123 | hp2 | a0003 | c0004 | t0004 | g0207 | AMR | CLM | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03471 | hp1 | a0005 | c0008 | t0001 | g0224 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | MSL | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
HG06807 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | USA | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
NA21309 | hp2 | a0009 | c0018 | t0001 | g0193 | AFR | LWK | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0004 | g0201 | REF | REF | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0256 | REF | REF | PKD2_chr4_88002635_88082777 | PKD2 | chr4 | 88002635 | 88082777 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:88007816
|
G | C | 2 | a0003a0007 | 35 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(32): Show |
missense_variant | MODERATE | c.83G>C | p.Arg28Pro | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 182/5089 | 83/2907 | 28/968 | chr4 | 88007816 | ||
chr4:88008021
|
C | CGAG | 1 | a0005 | 3 | HG02572.hp1 HG02896.hp1 HG03471.hp1 |
disruptive_inframe_insertion | MODERATE | c.305_307dupAGG | p.Glu102dup | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 407/5089 | 308/2907 | 103/968 | INFO_REALIGN_3_PRIME | chr4 | 88008021 | |
chr4:88008301
|
G | A | 3 | a0002a0010a0011 | 48 | HG00609.hp1 HG01516.hp1 HG01928.hp1 others(45): Show |
missense_variant | MODERATE | c.568G>A | p.Ala190Thr | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 667/5089 | 568/2907 | 190/968 | chr4 | 88008301 | ||
chr4:88046676
|
A | G | 2 | a0004a0011 | 9 | HG00558.hp2 HG02040.hp2 HG02129.hp1 others(6): Show |
missense_variant | MODERATE | c.1354A>G | p.Ile452Val | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/15 | 1453/5089 | 1354/2907 | 452/968 | chr4 | 88046676 | ||
chr4:88056102
|
A | G | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1733A>G | p.Asn578Ser | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/15 | 1832/5089 | 1733/2907 | 578/968 | chr4 | 88056102 | ||
chr4:88067937
|
A | C | 2 | a0007a0008 | 2 | HG01255.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.2398A>C | p.Met800Leu | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/15 | 2497/5089 | 2398/2907 | 800/968 | chr4 | 88067937 | ||
chr4:88067950
|
G | A | 1 | a0006 | 2 | HG01981.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.2411G>A | p.Ser804Asn | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/15 | 2510/5089 | 2411/2907 | 804/968 | chr4 | 88067950 | ||
chr4:88074832
|
G | A | 1 | a0010 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.2543G>A | p.Arg848Gln | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 14/15 | 2642/5089 | 2543/2907 | 848/968 | chr4 | 88074832 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:88008153
|
G | A | 3 | a0001c0002a0001c0017a0009c0018 | 84 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
synonymous_variant | LOW | c.420G>A | p.Gly140Gly | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 519/5089 | 420/2907 | 140/968 | chr4 | 88008153 | ||
chr4:88008177
|
C | T | 1 | a0001c0013 | 2 | NA19043.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.444C>T | p.Gly148Gly | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 543/5089 | 444/2907 | 148/968 | chr4 | 88008177 | ||
chr4:88008303
|
G | T | 1 | a0001c0006 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.570G>T | p.Ala190Ala | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 669/5089 | 570/2907 | 190/968 | chr4 | 88008303 | ||
chr4:88046681
|
A | G | 3 | a0001c0012a0003c0015a0005c0008 | 5 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.1359A>G | p.Pro453Pro | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/15 | 1458/5089 | 1359/2907 | 453/968 | chr4 | 88046681 | ||
chr4:88052059
|
G | C | 1 | a0001c0022 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1617G>C | p.Leu539Leu | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/15 | 1716/5089 | 1617/2907 | 539/968 | chr4 | 88052059 | ||
chr4:88056199
|
G | A | 1 | a0001c0009 | 2 | HG01891.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.1830G>A | p.Ala610Ala | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/15 | 1929/5089 | 1830/2907 | 610/968 | chr4 | 88056199 | ||
chr4:88065389
|
T | C | 2 | a0001c0010a0003c0007 | 5 | HG01167.hp1 HG01192.hp2 HG02055.hp2 others(2): Show |
synonymous_variant | LOW | c.2134T>C | p.Leu712Leu | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 11/15 | 2233/5089 | 2134/2907 | 712/968 | chr4 | 88065389 | ||
chr4:88065394
|
C | T | 1 | a0001c0017 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2139C>T | p.Val713Val | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 11/15 | 2238/5089 | 2139/2907 | 713/968 | chr4 | 88065394 | ||
chr4:88065816
|
T | C | 1 | a0002c0019 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.2295T>C | p.Asp765Asp | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/15 | 2394/5089 | 2295/2907 | 765/968 | chr4 | 88065816 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:88007652
|
G | C | 2 | a0001c0001t0006a0001c0001t0007 | 2 | HG02647.hp2 HG02738.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 82 | chr4 | 88007652 | |||||
chr4:88007716
|
C | G | 1 | a0001c0001t0015 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/15 | 18 | chr4 | 88007716 | |||||
chr4:88075933
|
T | G | 1 | a0001c0001t0008 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 239 | chr4 | 88075933 | |||||
chr4:88075950
|
C | T | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(11): Show | 110 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 256 | chr4 | 88075950 | |||||
chr4:88076078
|
T | C | 1 | a0001c0001t0008 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 384 | chr4 | 88076078 | |||||
chr4:88076531
|
C | G | 1 | a0003c0004t0005 | 8 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*837C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 837 | chr4 | 88076531 | |||||
chr4:88076651
|
T | A | 1 | a0001c0001t0009 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*957T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 957 | chr4 | 88076651 | |||||
chr4:88076724
|
G | A | 4 | a0001c0001t0002a0001c0002t0002a0001c0017t0002others(1): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1030G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1030 | chr4 | 88076724 | |||||
chr4:88076751
|
C | T | 1 | a0001c0001t0014 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1057C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1057 | chr4 | 88076751 | |||||
chr4:88076782
|
T | G | 1 | a0001c0001t0010 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1088 | chr4 | 88076782 | |||||
chr4:88076870
|
G | T | 1 | a0001c0001t0013 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1176 | chr4 | 88076870 | |||||
chr4:88076931
|
G | A | 5 | a0001c0001t0004a0001c0010t0004a0003c0004t0004others(2): Show | 32 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1237 | chr4 | 88076931 | |||||
chr4:88076996
|
C | T | 1 | a0001c0001t0012 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1302C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1302 | chr4 | 88076996 | |||||
chr4:88077305
|
T | G | 1 | a0001c0001t0011 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1611T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1611 | chr4 | 88077305 | |||||
chr4:88077433
|
C | T | 1 | a0001c0001t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 15/15 | 1739 | chr4 | 88077433 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:88008343
|
C | T | 1 | a0002c0003t0003g0311 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.595+15C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008343 | ||||||
chr4:88008503
|
G | A | 14 | a0003c0004t0001g0030a0003c0004t0001g0031a0003c0004t0005g0019others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.595+175G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008503 | ||||||
chr4:88008535
|
T | C | 223 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(220): Show | 254 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.595+207T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008535 | ||||||
chr4:88008660
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.595+332A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008660 | ||||||
chr4:88008765
|
T | A | 2 | a0001c0013t0003g0033a0001c0013t0003g0034 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.595+437T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008765 | ||||||
chr4:88008769
|
C | T | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+441C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008769 | ||||||
chr4:88008853
|
G | A | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+525G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008853 | ||||||
chr4:88008887
|
A | G | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+559A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88008887 | ||||||
chr4:88009018
|
G | T | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+690G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009018 | ||||||
chr4:88009109
|
C | T | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+781C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009109 | ||||||
chr4:88009420
|
C | A | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1092C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009420 | ||||||
chr4:88009477
|
A | C | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1149A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009477 | ||||||
chr4:88009490
|
A | AT | 11 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.595+1176dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88009490 | |||||
chr4:88009490
|
AT | A | 109 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 118 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.595+1176delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88009490 | |||||
chr4:88009529
|
A | C | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1201A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009529 | ||||||
chr4:88009590
|
T | C | 1 | a0001c0017t0002g0134 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.595+1262T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009590 | ||||||
chr4:88009624
|
T | C | 63 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(60): Show | 67 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.595+1296T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009624 | ||||||
chr4:88009670
|
A | C | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1342A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009670 | ||||||
chr4:88009689
|
G | A | 230 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.595+1361G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009689 | ||||||
chr4:88009708
|
C | A | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595+1380C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009708 | ||||||
chr4:88009736
|
A | T | 63 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(60): Show | 67 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.595+1408A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009736 | ||||||
chr4:88009898
|
C | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 217 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.595+1570C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009898 | ||||||
chr4:88009992
|
G | A | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1664G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88009992 | ||||||
chr4:88010094
|
AT | A | 12 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0006g0219others(9): Show | 12 | HG00323.hp1 HG01928.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.595+1782delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88010094 | |||||
chr4:88010116
|
T | G | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1788T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010116 | ||||||
chr4:88010117
|
C | T | 3 | a0001c0001t0001g0195a0001c0013t0003g0033a0001c0013t0003g0034 | 3 | NA18906.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.595+1789C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010117 | ||||||
chr4:88010118
|
G | A | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1790G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010118 | ||||||
chr4:88010151
|
G | A | 12 | a0002c0003t0001g0035a0002c0003t0001g0039a0002c0003t0001g0041others(9): Show | 14 | HG01928.hp1 HG01952.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.595+1823G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010151 | ||||||
chr4:88010158
|
A | G | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1830A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010158 | ||||||
chr4:88010173
|
C | T | 1 | a0001c0017t0002g0134 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.595+1845C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010173 | ||||||
chr4:88010294
|
T | C | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+1966T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010294 | ||||||
chr4:88010307
|
C | A | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 66 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.595+1979C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010307 | ||||||
chr4:88010368
|
G | A | 4 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(1): Show | 4 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+2040G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010368 | ||||||
chr4:88010369
|
T | C | 36 | a0001c0001t0004g0196a0001c0001t0004g0197a0003c0004t0001g0030others(33): Show | 37 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.595+2041T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010369 | ||||||
chr4:88010379
|
A | G | 1 | a0001c0002t0001g0194 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.595+2051A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010379 | ||||||
chr4:88010839
|
T | A | 1 | a0002c0003t0001g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.595+2511T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010839 | ||||||
chr4:88010856
|
T | C | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 66 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.595+2528T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010856 | ||||||
chr4:88010877
|
T | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 53 | HG00733.hp2 HG00735.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.595+2549T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88010877 | ||||||
chr4:88011085
|
G | C | 1 | a0001c0001t0001g0232 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.595+2757G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011085 | ||||||
chr4:88011098
|
A | G | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+2770A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011098 | ||||||
chr4:88011106
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.595+2778A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011106 | ||||||
chr4:88011120
|
C | T | 64 | a0001c0002t0001g0138a0001c0002t0001g0146a0001c0002t0001g0156others(61): Show | 84 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.595+2792C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011120 | ||||||
chr4:88011149
|
A | G | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.595+2821A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011149 | ||||||
chr4:88011149
|
A | T | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+2821A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011149 | ||||||
chr4:88011264
|
T | C | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.595+2936T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011264 | ||||||
chr4:88011312
|
C | T | 40 | a0001c0001t0001g0141a0001c0001t0001g0195a0001c0001t0015g0143others(37): Show | 41 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.595+2984C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011312 | ||||||
chr4:88011326
|
C | CT | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG01081.hp1 HG02922.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.595+3012dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011326 | |||||
chr4:88011493
|
G | A | 1 | a0005c0008t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.595+3165G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011493 | ||||||
chr4:88011521
|
C | G | 1 | a0009c0018t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.595+3193C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011521 | ||||||
chr4:88011558
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.595+3230A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011558 | ||||||
chr4:88011670
|
C | A | 2 | a0001c0001t0001g0141a0001c0012t0003g0142 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.595+3342C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011670 | ||||||
chr4:88011715
|
G | C | 12 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+3387G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011715 | ||||||
chr4:88011724
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.595+3396T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011724 | ||||||
chr4:88011800
|
A | G | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+3472A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011800 | ||||||
chr4:88011883
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.595+3555A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011883 | ||||||
chr4:88011893
|
T | TG | 31 | a0001c0001t0001g0223a0001c0001t0001g0233a0001c0001t0001g0282others(28): Show | 31 | HG00597.hp2 HG01099.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.595+3578dupG | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011893 | |||||
chr4:88011893
|
TG | T | 56 | a0001c0001t0001g0128a0001c0001t0001g0234a0001c0001t0001g0240others(53): Show | 62 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.595+3578delG | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011893 | |||||
chr4:88011893
|
TGG | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 81 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.595+3577_595+3578d others(4): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011893 | |||||
chr4:88011893
|
TGGG | T | 53 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0097others(50): Show | 54 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.595+3576_595+3578d others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011893 | |||||
chr4:88011893
|
TGGGG | T | 66 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(63): Show | 70 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.595+3575_595+3578d others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88011893 | |||||
chr4:88011899
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.595+3571G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011899 | ||||||
chr4:88011910
|
G | C | 2 | a0001c0001t0010g0221a0001c0001t0012g0222 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+3582G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88011910 | ||||||
chr4:88012074
|
C | G | 3 | a0001c0001t0010g0221a0001c0001t0012g0222a0001c0022t0001g0304 | 3 | HG02145.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.595+3746C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012074 | ||||||
chr4:88012124
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02148.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.595+3796T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012124 | ||||||
chr4:88012200
|
T | C | 5 | a0001c0001t0001g0141a0001c0001t0010g0221a0001c0001t0012g0222others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+3872T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012200 | ||||||
chr4:88012219
|
A | G | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+3891A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012219 | ||||||
chr4:88012237
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.595+3909C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012237 | ||||||
chr4:88012258
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | NA18995.hp1 NA19011.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+3930G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012258 | ||||||
chr4:88012277
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.595+3949C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012277 | ||||||
chr4:88012367
|
A | G | 2 | a0001c0001t0006g0219a0001c0001t0007g0220 | 2 | HG02647.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.595+4039A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012367 | ||||||
chr4:88012432
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(221): Show | 255 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.595+4104C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012432 | ||||||
chr4:88012443
|
C | T | 3 | a0005c0008t0001g0224a0005c0008t0003g0225a0005c0016t0001g0226 | 3 | HG02572.hp1 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.595+4115C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012443 | ||||||
chr4:88012468
|
T | TA | 229 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.595+4142dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88012468 | |||||
chr4:88012473
|
A | G | 67 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(64): Show | 71 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.595+4145A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012473 | ||||||
chr4:88012620
|
G | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(223): Show | 257 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.595+4292G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012620 | ||||||
chr4:88012656
|
A | G | 226 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(223): Show | 257 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.595+4328A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012656 | ||||||
chr4:88012671
|
CTTT | C | 4 | a0003c0004t0004g0199a0003c0004t0004g0200a0003c0004t0004g0201others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+4347_595+4349d others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88012671 | |||||
chr4:88012695
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.595+4367C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012695 | ||||||
chr4:88012749
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595+4421C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012749 | ||||||
chr4:88012886
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.595+4558G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88012886 | ||||||
chr4:88013320
|
G | A | 2 | a0001c0001t0001g0141a0001c0012t0003g0142 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.595+4992G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88013320 | ||||||
chr4:88013345
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.595+5017G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88013345 | ||||||
chr4:88013640
|
T | C | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 66 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.595+5312T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88013640 | ||||||
chr4:88013709
|
T | TAA | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 66 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.595+5394_595+5395d others(4): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88013709 | |||||
chr4:88013770
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.595+5442G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88013770 | ||||||
chr4:88013803
|
A | G | 227 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 258 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.595+5475A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88013803 | ||||||
chr4:88014011
|
G | A | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0282others(1): Show | 4 | HG00642.hp2 HG01123.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-5447G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014011 | ||||||
chr4:88014036
|
G | A | 3 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0162 | 3 | NA18947.hp1 NA18963.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.596-5422G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014036 | ||||||
chr4:88014079
|
A | G | 228 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 259 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.596-5379A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014079 | ||||||
chr4:88014352
|
T | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0107others(2): Show | 5 | HG01981.hp2 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-5106T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014352 | ||||||
chr4:88014422
|
C | G | 1 | a0001c0002t0002g0159 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.596-5036C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014422 | ||||||
chr4:88014486
|
T | TA | 55 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 60 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.596-4957dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88014486 | |||||
chr4:88014486
|
T | TAA | 127 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(124): Show | 151 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.596-4958_596-4957d others(4): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88014486 | |||||
chr4:88014486
|
T | TAAA | 42 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0103others(39): Show | 44 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.596-4959_596-4957d others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88014486 | |||||
chr4:88014585
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.596-4873C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014585 | ||||||
chr4:88014737
|
G | A | 2 | a0001c0001t0001g0141a0001c0012t0003g0142 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.596-4721G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014737 | ||||||
chr4:88014920
|
C | G | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-4538C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88014920 | ||||||
chr4:88015030
|
C | T | 3 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249 | 3 | HG02015.hp2 HG02083.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.596-4428C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015030 | ||||||
chr4:88015034
|
A | G | 1 | a0002c0003t0003g0042 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.596-4424A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015034 | ||||||
chr4:88015320
|
G | A | 2 | a0001c0001t0001g0228a0001c0009t0001g0229 | 2 | HG00639.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.596-4138G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015320 | ||||||
chr4:88015472
|
G | A | 3 | a0005c0008t0001g0224a0005c0008t0003g0225a0005c0016t0001g0226 | 3 | HG02572.hp1 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.596-3986G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015472 | ||||||
chr4:88015506
|
G | A | 1 | a0004c0005t0001g0252 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.596-3952G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015506 | ||||||
chr4:88015558
|
T | G | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-3900T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88015558 | ||||||
chr4:88016115
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.596-3343G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016115 | ||||||
chr4:88016119
|
C | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG01433.hp1 HG01928.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-3339C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016119 | ||||||
chr4:88016339
|
T | C | 133 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(130): Show | 157 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.596-3119T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016339 | ||||||
chr4:88016352
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.596-3106A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016352 | ||||||
chr4:88016705
|
A | T | 2 | a0002c0003t0001g0085a0002c0003t0001g0086 | 2 | NA18972.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.596-2753A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016705 | ||||||
chr4:88016717
|
T | C | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.596-2741T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016717 | ||||||
chr4:88016915
|
A | G | 65 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(62): Show | 69 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.596-2543A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016915 | ||||||
chr4:88016922
|
T | C | 65 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(62): Show | 69 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.596-2536T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88016922 | ||||||
chr4:88017017
|
A | G | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.596-2441A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017017 | ||||||
chr4:88017180
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.596-2278C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017180 | ||||||
chr4:88017478
|
T | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 56 | HG00733.hp2 HG00735.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.596-1980T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017478 | ||||||
chr4:88017513
|
G | A | 1 | a0002c0003t0003g0037 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.596-1945G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017513 | ||||||
chr4:88017530
|
C | G | 1 | a0001c0002t0001g0158 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.596-1928C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017530 | ||||||
chr4:88017538
|
T | C | 4 | a0003c0004t0005g0019a0003c0007t0004g0020a0003c0007t0004g0021others(1): Show | 4 | HG02055.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-1920T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017538 | ||||||
chr4:88017540
|
G | A | 1 | a0010c0020t0001g0054 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.596-1918G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017540 | ||||||
chr4:88017748
|
A | G | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-1710A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017748 | ||||||
chr4:88017770
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.596-1688C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017770 | ||||||
chr4:88017848
|
C | A | 62 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 66 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.596-1610C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88017848 | ||||||
chr4:88018029
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0128 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.596-1429A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018029 | ||||||
chr4:88018290
|
G | T | 12 | a0001c0001t0001g0233a0001c0001t0001g0247a0001c0001t0001g0279others(9): Show | 12 | HG00558.hp1 HG00597.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-1168G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018290 | ||||||
chr4:88018301
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.596-1157T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018301 | ||||||
chr4:88018306
|
A | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-1152A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018306 | ||||||
chr4:88018584
|
A | G | 64 | a0001c0002t0001g0138a0001c0002t0001g0146a0001c0002t0001g0156others(61): Show | 84 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.596-874A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018584 | ||||||
chr4:88018922
|
G | A | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.596-536G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88018922 | ||||||
chr4:88019014
|
T | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-444T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019014 | ||||||
chr4:88019033
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.596-425T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019033 | ||||||
chr4:88019154
|
C | T | 1 | a0008c0023t0003g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.596-304C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019154 | ||||||
chr4:88019177
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.596-281C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019177 | ||||||
chr4:88019277
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-181A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019277 | ||||||
chr4:88019294
|
C | A | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-164C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019294 | ||||||
chr4:88019327
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-131A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019327 | ||||||
chr4:88019329
|
TA | T | 67 | a0001c0001t0001g0195a0001c0002t0001g0138a0001c0002t0001g0146others(64): Show | 87 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.596-116delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr4 | 88019329 | |||||
chr4:88019371
|
T | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0004g0106others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-87T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019371 | ||||||
chr4:88019442
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0120 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.596-16C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 1/14 | chr4 | 88019442 | ||||||
chr4:88019820
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.709+249A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88019820 | ||||||
chr4:88019871
|
G | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01081.hp1 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+300G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88019871 | ||||||
chr4:88019981
|
A | G | 3 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229 | 3 | HG00639.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.709+410A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88019981 | ||||||
chr4:88020064
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.709+493G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020064 | ||||||
chr4:88020120
|
C | T | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.709+549C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020120 | ||||||
chr4:88020322
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.709+751G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020322 | ||||||
chr4:88020397
|
C | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 118 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.709+826C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020397 | ||||||
chr4:88020445
|
A | G | 2 | a0001c0013t0003g0033a0001c0013t0003g0034 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.709+874A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020445 | ||||||
chr4:88020493
|
G | A | 1 | a0002c0003t0001g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.709+922G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020493 | ||||||
chr4:88020683
|
CT | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0283a0001c0002t0002g0137others(5): Show | 8 | HG00323.hp1 HG01167.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.709+1130delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88020683 | |||||
chr4:88020742
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.709+1171T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020742 | ||||||
chr4:88020943
|
T | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 259 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.709+1372T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88020943 | ||||||
chr4:88021338
|
G | A | 1 | a0001c0001t0006g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.709+1767G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88021338 | ||||||
chr4:88021432
|
G | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 120 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.709+1861G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88021432 | ||||||
chr4:88021595
|
G | A | 1 | a0002c0003t0003g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.709+2024G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88021595 | ||||||
chr4:88021674
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.709+2103T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88021674 | ||||||
chr4:88021992
|
C | T | 1 | a0002c0003t0003g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.709+2421C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88021992 | ||||||
chr4:88022037
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0004g0106others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+2466C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022037 | ||||||
chr4:88022077
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.709+2506G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022077 | ||||||
chr4:88022735
|
A | T | 216 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(213): Show | 246 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.709+3164A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022735 | ||||||
chr4:88022953
|
C | T | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+3382C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022953 | ||||||
chr4:88022983
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.709+3412A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022983 | ||||||
chr4:88022985
|
G | A | 1 | a0004c0005t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.709+3414G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022985 | ||||||
chr4:88022992
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.709+3421A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88022992 | ||||||
chr4:88023037
|
C | T | 1 | a0001c0001t0004g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.709+3466C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88023037 | ||||||
chr4:88023141
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.709+3570G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88023141 | ||||||
chr4:88023359
|
C | T | 175 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(172): Show | 204 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.709+3788C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88023359 | ||||||
chr4:88023642
|
TA | T | 6 | a0001c0002t0001g0157a0001c0002t0001g0186a0001c0002t0001g0187others(3): Show | 6 | HG01074.hp2 HG01934.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.709+4073delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88023642 | |||||
chr4:88023901
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.709+4330A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88023901 | ||||||
chr4:88023991
|
C | G | 3 | a0001c0001t0001g0195a0001c0013t0003g0033a0001c0013t0003g0034 | 3 | NA18906.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.709+4420C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88023991 | ||||||
chr4:88024049
|
C | T | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.709+4478C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024049 | ||||||
chr4:88024071
|
A | G | 11 | a0001c0002t0001g0156a0001c0002t0002g0002a0001c0002t0002g0015others(8): Show | 17 | HG00609.hp2 HG02071.hp1 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.709+4500A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024071 | ||||||
chr4:88024101
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.709+4530A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024101 | ||||||
chr4:88024147
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.709+4576G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024147 | ||||||
chr4:88024313
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.709+4742C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024313 | ||||||
chr4:88024429
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.709+4858C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024429 | ||||||
chr4:88024445
|
AC | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.709+4875delC | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024445 | ||||||
chr4:88024456
|
C | CG | 3 | a0001c0002t0002g0145a0001c0002t0002g0159a0001c0002t0002g0185 | 3 | HG02129.hp2 NA19066.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.709+4886dupG | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88024456 | |||||
chr4:88024457
|
G | GA | 23 | a0001c0001t0001g0233a0001c0001t0001g0254a0001c0001t0001g0255others(20): Show | 24 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.709+4911dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88024457 | |||||
chr4:88024457
|
GA | G | 21 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0102others(18): Show | 21 | HG00609.hp1 HG01256.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.709+4911delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88024457 | |||||
chr4:88024457
|
GAA | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 107 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(104): Show |
intron_variant | MODIFIER | c.709+4910_709+4911d others(4): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88024457 | |||||
chr4:88024458
|
A | G | 62 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0002t0001g0138others(59): Show | 82 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.709+4887A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024458 | ||||||
chr4:88024459
|
A | G | 1 | a0001c0002t0002g0150 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.709+4888A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024459 | ||||||
chr4:88024479
|
A | G | 64 | a0001c0002t0001g0138a0001c0002t0001g0146a0001c0002t0001g0156others(61): Show | 84 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.709+4908A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024479 | ||||||
chr4:88024508
|
A | G | 1 | a0002c0003t0003g0311 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.709+4937A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024508 | ||||||
chr4:88024626
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.709+5055A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024626 | ||||||
chr4:88024949
|
A | G | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+5378A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88024949 | ||||||
chr4:88025064
|
C | T | 1 | a0001c0002t0002g0139 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.709+5493C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025064 | ||||||
chr4:88025239
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 48 | HG00733.hp2 HG00735.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.709+5668A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025239 | ||||||
chr4:88025319
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.709+5748A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025319 | ||||||
chr4:88025613
|
CA | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 21 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.709+6056delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88025613 | |||||
chr4:88025632
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.709+6061A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025632 | ||||||
chr4:88025724
|
C | T | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+6153C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025724 | ||||||
chr4:88025725
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229 | 3 | HG00639.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.709+6154C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025725 | ||||||
chr4:88025833
|
T | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0004g0106others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+6262T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025833 | ||||||
chr4:88025869
|
C | T | 21 | a0003c0004t0001g0203a0003c0004t0001g0209a0003c0004t0001g0210others(18): Show | 22 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.709+6298C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025869 | ||||||
chr4:88025971
|
C | T | 2 | a0001c0001t0001g0275a0001c0001t0001g0296 | 2 | NA19012.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.709+6400C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88025971 | ||||||
chr4:88026280
|
T | C | 2 | a0005c0008t0001g0224a0005c0008t0003g0225 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.709+6709T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026280 | ||||||
chr4:88026318
|
C | T | 1 | a0002c0003t0003g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.709+6747C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026318 | ||||||
chr4:88026428
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.709+6857C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026428 | ||||||
chr4:88026580
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.709+7009A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026580 | ||||||
chr4:88026678
|
C | T | 1 | a0009c0018t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.709+7107C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026678 | ||||||
chr4:88026717
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 120 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.709+7146G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026717 | ||||||
chr4:88026881
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.709+7310A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88026881 | ||||||
chr4:88027047
|
T | C | 2 | a0001c0013t0003g0033a0001c0013t0003g0034 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.709+7476T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88027047 | ||||||
chr4:88027188
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.709+7617G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88027188 | ||||||
chr4:88027240
|
G | C | 1 | a0001c0001t0001g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.709+7669G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88027240 | ||||||
chr4:88027385
|
G | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.709+7814G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88027385 | ||||||
chr4:88027704
|
G | A | 2 | a0004c0005t0001g0278a0004c0005t0001g0297 | 2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.709+8133G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88027704 | ||||||
chr4:88027764
|
TC | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0004g0106others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+8198delC | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88027764 | |||||
chr4:88027828
|
T | TG | 310 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(307): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.709+8260dupG | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88027828 | |||||
chr4:88028023
|
G | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 216 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.710-8197G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028023 | ||||||
chr4:88028210
|
T | C | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710-8010T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028210 | ||||||
chr4:88028374
|
G | A | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.710-7846G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028374 | ||||||
chr4:88028489
|
G | A | 1 | a0001c0001t0009g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.710-7731G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028489 | ||||||
chr4:88028547
|
G | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0107others(2): Show | 5 | HG01981.hp2 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-7673G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028547 | ||||||
chr4:88028669
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-7551T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028669 | ||||||
chr4:88028708
|
C | T | 1 | a0001c0002t0001g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.710-7512C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028708 | ||||||
chr4:88028765
|
G | A | 38 | a0001c0001t0004g0140a0001c0001t0010g0221a0001c0001t0015g0143others(35): Show | 39 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.710-7455G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028765 | ||||||
chr4:88028783
|
T | TCACTTTT others(323): Show |
1 | a0002c0003t0003g0061 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.710-7423_710-7422i others(332): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88028783 | |||||
chr4:88028843
|
T | A | 2 | a0001c0013t0003g0033a0001c0013t0003g0034 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.710-7377T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028843 | ||||||
chr4:88028863
|
T | C | 1 | a0001c0012t0003g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.710-7357T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028863 | ||||||
chr4:88028980
|
A | T | 2 | a0001c0001t0006g0219a0001c0001t0007g0220 | 2 | HG02647.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.710-7240A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88028980 | ||||||
chr4:88029228
|
G | A | 8 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0004g0106others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.710-6992G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029228 | ||||||
chr4:88029237
|
T | C | 2 | a0003c0004t0005g0025a0003c0004t0005g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.710-6983T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029237 | ||||||
chr4:88029362
|
C | T | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.710-6858C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029362 | ||||||
chr4:88029378
|
T | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.710-6842T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029378 | ||||||
chr4:88029392
|
C | A | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710-6828C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029392 | ||||||
chr4:88029430
|
G | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01081.hp1 HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.710-6790G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029430 | ||||||
chr4:88029442
|
G | T | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.710-6778G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029442 | ||||||
chr4:88029477
|
A | G | 1 | a0002c0003t0003g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.710-6743A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029477 | ||||||
chr4:88029687
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.710-6533A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029687 | ||||||
chr4:88029730
|
A | T | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-6490A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029730 | ||||||
chr4:88029734
|
C | T | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-6486C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029734 | ||||||
chr4:88029916
|
A | G | 3 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229 | 3 | HG00639.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.710-6304A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88029916 | ||||||
chr4:88030161
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-6059T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030161 | ||||||
chr4:88030203
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.710-6017G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030203 | ||||||
chr4:88030227
|
C | T | 1 | a0001c0001t0003g0301 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.710-5993C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030227 | ||||||
chr4:88030238
|
G | A | 35 | a0003c0004t0001g0030a0003c0004t0001g0031a0003c0004t0001g0203others(32): Show | 36 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.710-5982G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030238 | ||||||
chr4:88030241
|
C | T | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-5979C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030241 | ||||||
chr4:88030355
|
T | G | 1 | a0003c0004t0004g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.710-5865T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030355 | ||||||
chr4:88030420
|
T | C | 5 | a0001c0002t0001g0138a0001c0002t0001g0164a0001c0002t0001g0165others(2): Show | 5 | NA18957.hp2 NA18961.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.710-5800T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030420 | ||||||
chr4:88030484
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.710-5736C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030484 | ||||||
chr4:88030665
|
C | T | 2 | a0001c0001t0006g0219a0001c0001t0007g0220 | 2 | HG02647.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.710-5555C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030665 | ||||||
chr4:88030676
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229 | 3 | HG00639.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.710-5544G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030676 | ||||||
chr4:88030724
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.710-5496A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030724 | ||||||
chr4:88030730
|
G | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02148.hp2 HG03710.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-5490G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030730 | ||||||
chr4:88030769
|
G | T | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710-5451G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030769 | ||||||
chr4:88030854
|
G | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-5366G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030854 | ||||||
chr4:88030924
|
T | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 205 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.710-5296T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030924 | ||||||
chr4:88030984
|
C | T | 229 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.710-5236C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88030984 | ||||||
chr4:88031152
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.710-5068A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031152 | ||||||
chr4:88031156
|
T | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-5064T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031156 | ||||||
chr4:88031192
|
A | G | 2 | a0002c0019t0001g0080a0010c0020t0001g0054 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.710-5028A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031192 | ||||||
chr4:88031211
|
T | C | 1 | a0001c0002t0001g0164 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.710-5009T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031211 | ||||||
chr4:88031292
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4928T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031292 | ||||||
chr4:88031324
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710-4896A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031324 | ||||||
chr4:88031333
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4887T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031333 | ||||||
chr4:88031334
|
A | G | 2 | a0001c0001t0006g0219a0001c0001t0007g0220 | 2 | HG02647.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.710-4886A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031334 | ||||||
chr4:88031450
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4770A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031450 | ||||||
chr4:88031485
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4735T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031485 | ||||||
chr4:88031531
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4689A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031531 | ||||||
chr4:88031696
|
A | C | 1 | a0001c0002t0001g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.710-4524A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031696 | ||||||
chr4:88031731
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 205 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.710-4489A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031731 | ||||||
chr4:88031776
|
G | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4444G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031776 | ||||||
chr4:88031849
|
T | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4371T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031849 | ||||||
chr4:88031878
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.710-4342A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88031878 | ||||||
chr4:88032014
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-4206A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88032014 | ||||||
chr4:88032482
|
G | C | 1 | a0001c0001t0012g0222 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.710-3738G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88032482 | ||||||
chr4:88032488
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.710-3732T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88032488 | ||||||
chr4:88032567
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.710-3653T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88032567 | ||||||
chr4:88032964
|
C | T | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.710-3256C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88032964 | ||||||
chr4:88033095
|
G | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 119 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.710-3125G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033095 | ||||||
chr4:88033248
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710-2972G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033248 | ||||||
chr4:88033255
|
C | T | 36 | a0001c0001t0004g0140a0003c0004t0001g0030a0003c0004t0001g0031others(33): Show | 37 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.710-2965C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033255 | ||||||
chr4:88033256
|
G | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 119 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.710-2964G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033256 | ||||||
chr4:88033271
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.710-2949T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033271 | ||||||
chr4:88033371
|
G | A | 63 | a0001c0002t0001g0138a0001c0002t0001g0146a0001c0002t0001g0156others(60): Show | 83 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.710-2849G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033371 | ||||||
chr4:88033653
|
A | C | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-2567A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033653 | ||||||
chr4:88033863
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0002g0120 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.710-2357T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88033863 | ||||||
chr4:88034015
|
G | A | 3 | a0001c0002t0001g0157a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01934.hp2 HG01981.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.710-2205G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034015 | ||||||
chr4:88034026
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.710-2194G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034026 | ||||||
chr4:88034451
|
C | G | 60 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(57): Show | 64 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.710-1769C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034451 | ||||||
chr4:88034494
|
C | A | 2 | a0001c0001t0001g0228a0001c0009t0001g0229 | 2 | HG00639.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.710-1726C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034494 | ||||||
chr4:88034610
|
G | A | 21 | a0001c0002t0001g0156a0001c0002t0001g0158a0001c0002t0002g0001others(18): Show | 36 | HG00609.hp2 HG02027.hp1 HG02071.hp1 others(33): Show |
intron_variant | MODIFIER | c.710-1610G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034610 | ||||||
chr4:88034616
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.710-1604C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034616 | ||||||
chr4:88034664
|
G | A | 3 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0012g0222 | 3 | HG02647.hp2 HG02738.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.710-1556G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034664 | ||||||
chr4:88034668
|
C | CA | 95 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0102others(92): Show | 95 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.710-1532dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88034668 | |||||
chr4:88034668
|
CA | C | 31 | a0001c0001t0001g0090a0001c0001t0001g0119a0001c0002t0001g0138others(28): Show | 34 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.710-1532delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88034668 | |||||
chr4:88034691
|
C | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 214 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.710-1529C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034691 | ||||||
chr4:88034862
|
C | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0283 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.710-1358C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034862 | ||||||
chr4:88034943
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.710-1277G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88034943 | ||||||
chr4:88035086
|
T | C | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-1134T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035086 | ||||||
chr4:88035197
|
T | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(8): Show | 11 | HG00099.hp1 HG00733.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.710-1023T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035197 | ||||||
chr4:88035345
|
G | A | 3 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218 | 4 | HG01884.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-875G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035345 | ||||||
chr4:88035369
|
A | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 119 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.710-851A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035369 | ||||||
chr4:88035699
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710-521G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035699 | ||||||
chr4:88035899
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710-321G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88035899 | ||||||
chr4:88036027
|
CT | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0022t0001g0304 | 3 | HG02145.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.710-189delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 88036027 | |||||
chr4:88036069
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.710-151A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88036069 | ||||||
chr4:88036123
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.710-97T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88036123 | ||||||
chr4:88036145
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.710-75C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88036145 | ||||||
chr4:88036190
|
G | A | 1 | a0001c0002t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.710-30G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88036190 | ||||||
chr4:88036191
|
G | A | 3 | a0001c0001t0010g0221a0001c0013t0003g0033a0001c0013t0003g0034 | 3 | HG03209.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.710-29G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 2/14 | chr4 | 88036191 | ||||||
chr4:88036410
|
T | C | 31 | a0003c0004t0001g0030a0003c0004t0001g0203a0003c0004t0001g0209others(28): Show | 32 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.843+57T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036410 | ||||||
chr4:88036469
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843+116A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036469 | ||||||
chr4:88036571
|
C | A | 58 | a0001c0001t0002g0053a0001c0002t0001g0138a0001c0002t0001g0146others(55): Show | 78 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.843+218C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036571 | ||||||
chr4:88036595
|
A | G | 3 | a0001c0002t0001g0157a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01934.hp2 HG01981.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.843+242A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036595 | ||||||
chr4:88036760
|
A | G | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.843+407A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036760 | ||||||
chr4:88036842
|
C | G | 6 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229others(3): Show | 6 | HG00639.hp1 HG01167.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+489C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036842 | ||||||
chr4:88036904
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.843+551T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88036904 | ||||||
chr4:88037002
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.843+649G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037002 | ||||||
chr4:88037016
|
C | T | 8 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229others(5): Show | 8 | HG00639.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+663C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037016 | ||||||
chr4:88037221
|
T | C | 2 | a0001c0002t0002g0013a0001c0002t0002g0177 | 3 | HG03491.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.843+868T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037221 | ||||||
chr4:88037251
|
A | C | 1 | a0001c0002t0001g0138 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.843+898A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037251 | ||||||
chr4:88037340
|
G | A | 120 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0123others(117): Show | 142 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.844-911G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037340 | ||||||
chr4:88037631
|
T | C | 5 | a0001c0001t0006g0219a0001c0001t0007g0220a0001c0001t0010g0221others(2): Show | 5 | HG02647.hp2 HG02738.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-620T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037631 | ||||||
chr4:88037663
|
A | C | 8 | a0001c0001t0001g0228a0001c0001t0004g0106a0001c0009t0001g0229others(5): Show | 8 | HG00639.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-588A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037663 | ||||||
chr4:88037729
|
A | G | 1 | a0002c0003t0001g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.844-522A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037729 | ||||||
chr4:88037731
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0008g0096others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-520A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88037731 | ||||||
chr4:88037872
|
CAA | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(16): Show | 23 | HG00733.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-377_844-376del others(2): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 88037872 | |||||
chr4:88038229
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(208): Show | 241 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.844-22G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 3/14 | chr4 | 88038229 | ||||||
chr4:88038563
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1094+62C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038563 | ||||||
chr4:88038593
|
A | G | 74 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 79 | HG00099.hp1 HG00609.hp1 HG01243.hp1 others(76): Show |
intron_variant | MODIFIER | c.1094+92A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038593 | ||||||
chr4:88038770
|
G | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(136): Show | 164 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1094+269G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038770 | ||||||
chr4:88038809
|
T | C | 59 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0279others(56): Show | 79 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1094+308T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038809 | ||||||
chr4:88038816
|
G | C | 112 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0083others(109): Show | 133 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1094+315G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038816 | ||||||
chr4:88038825
|
T | A | 14 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1094+324T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038825 | ||||||
chr4:88038846
|
A | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(77): Show | 85 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.1094+345A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038846 | ||||||
chr4:88038958
|
C | A | 1 | a0001c0001t0001g0009 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1094+457C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88038958 | ||||||
chr4:88039008
|
A | G | 3 | a0001c0001t0001g0228a0001c0009t0001g0229a0003c0004t0001g0030 | 3 | HG00639.hp1 HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1094+507A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039008 | ||||||
chr4:88039106
|
A | T | 47 | a0001c0001t0002g0053a0001c0001t0002g0120a0001c0002t0001g0176others(44): Show | 67 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1094+605A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039106 | ||||||
chr4:88039153
|
C | T | 2 | a0001c0001t0006g0219a0003c0004t0001g0210 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1094+652C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039153 | ||||||
chr4:88039177
|
C | G | 26 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0083others(23): Show | 27 | HG00609.hp1 HG00639.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1094+676C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039177 | ||||||
chr4:88039183
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1094+682G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039183 | ||||||
chr4:88039225
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0004g0106a0001c0001t0004g0140others(1): Show | 4 | HG03471.hp2 HG03486.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1094+724A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039225 | ||||||
chr4:88039427
|
A | G | 145 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(142): Show | 171 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.1094+926A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039427 | ||||||
chr4:88039430
|
C | T | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1094+929C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039430 | ||||||
chr4:88039435
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0092others(23): Show | 30 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1094+934C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039435 | ||||||
chr4:88039660
|
C | A | 310 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(307): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.1094+1159C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039660 | ||||||
chr4:88039664
|
C | CA | 12 | a0001c0001t0001g0097a0001c0001t0001g0114a0001c0001t0001g0250others(9): Show | 12 | HG01361.hp1 HG01978.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.1094+1178dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 88039664 | |||||
chr4:88039664
|
C | CAA | 51 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0092others(48): Show | 56 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1094+1177_1094+117 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 88039664 | |||||
chr4:88039949
|
C | G | 1 | a0001c0002t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1094+1448C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88039949 | ||||||
chr4:88040032
|
G | A | 21 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0083others(18): Show | 22 | HG00609.hp1 HG01081.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.1094+1531G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040032 | ||||||
chr4:88040259
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1094+1758A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040259 | ||||||
chr4:88040302
|
C | G | 2 | a0002c0019t0001g0080a0010c0020t0001g0054 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1094+1801C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040302 | ||||||
chr4:88040353
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1094+1852G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040353 | ||||||
chr4:88040416
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1094+1915A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040416 | ||||||
chr4:88040419
|
C | T | 62 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(59): Show | 82 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1094+1918C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040419 | ||||||
chr4:88040584
|
A | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(143): Show | 172 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1094+2083A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88040584 | ||||||
chr4:88041408
|
C | T | 1 | a0001c0002t0002g0139 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1095-1825C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041408 | ||||||
chr4:88041529
|
C | A | 1 | a0002c0003t0003g0037 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1095-1704C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041529 | ||||||
chr4:88041634
|
T | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0092others(24): Show | 31 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1095-1599T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041634 | ||||||
chr4:88041779
|
T | C | 1 | a0003c0007t0004g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1095-1454T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041779 | ||||||
chr4:88041890
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1095-1343A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041890 | ||||||
chr4:88041928
|
C | T | 2 | a0002c0003t0001g0077a0002c0003t0001g0078 | 2 | NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1095-1305C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041928 | ||||||
chr4:88041987
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0117 | 3 | HG02109.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1095-1246C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88041987 | ||||||
chr4:88042020
|
G | A | 2 | a0005c0008t0001g0224a0005c0008t0003g0225 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1095-1213G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042020 | ||||||
chr4:88042089
|
G | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0002c0003t0001g0091 | 3 | NA18945.hp1 NA18953.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1095-1144G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042089 | ||||||
chr4:88042103
|
G | A | 31 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249others(28): Show | 33 | HG00597.hp2 HG01516.hp1 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.1095-1130G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042103 | ||||||
chr4:88042199
|
T | C | 2 | a0005c0008t0001g0224a0005c0008t0003g0225 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1095-1034T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042199 | ||||||
chr4:88042250
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0006g0219a0003c0004t0001g0210 | 3 | HG02738.hp2 HG04228.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1095-983C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042250 | ||||||
chr4:88042265
|
G | A | 1 | a0003c0004t0005g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1095-968G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042265 | ||||||
chr4:88042360
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1095-873A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042360 | ||||||
chr4:88042369
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1095-864G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042369 | ||||||
chr4:88042411
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1095-822G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042411 | ||||||
chr4:88042450
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0092others(51): Show | 59 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.1095-783A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042450 | ||||||
chr4:88042564
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1095-669C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042564 | ||||||
chr4:88042668
|
C | G | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1095-565C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042668 | ||||||
chr4:88042865
|
C | T | 3 | a0001c0012t0003g0111a0003c0004t0001g0031a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1095-368C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88042865 | ||||||
chr4:88043003
|
A | G | 1 | a0001c0002t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1095-230A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88043003 | ||||||
chr4:88043023
|
C | T | 1 | a0001c0006t0001g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1095-210C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88043023 | ||||||
chr4:88043027
|
A | T | 1 | a0001c0006t0001g0218 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1095-206A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88043027 | ||||||
chr4:88043109
|
C | T | 1 | a0002c0003t0001g0087 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1095-124C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 4/14 | chr4 | 88043109 | ||||||
chr4:88043615
|
G | A | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1319+158G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88043615 | ||||||
chr4:88043769
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0099 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1319+312G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88043769 | ||||||
chr4:88043804
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1319+347C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88043804 | ||||||
chr4:88043805
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1319+348C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88043805 | ||||||
chr4:88043927
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1319+470G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88043927 | ||||||
chr4:88044008
|
A | G | 3 | a0001c0001t0001g0227a0001c0001t0006g0219a0003c0004t0001g0210 | 3 | HG02738.hp2 HG04228.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1319+551A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044008 | ||||||
chr4:88044020
|
A | C | 4 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0004t0001g0031others(1): Show | 4 | HG01167.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1319+563A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044020 | ||||||
chr4:88044341
|
ACAT | A | 62 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(59): Show | 82 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1319+885_1319+887d others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044341 | ||||||
chr4:88044420
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1319+963G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044420 | ||||||
chr4:88044652
|
G | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0092others(18): Show | 25 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1319+1195G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044652 | ||||||
chr4:88044705
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1319+1248T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044705 | ||||||
chr4:88044728
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319+1271G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044728 | ||||||
chr4:88044757
|
A | G | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1319+1300A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044757 | ||||||
chr4:88044848
|
C | A | 11 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(8): Show | 12 | HG00609.hp1 HG01081.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1319+1391C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044848 | ||||||
chr4:88044906
|
A | C | 1 | a0002c0003t0001g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1319+1449A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88044906 | ||||||
chr4:88045075
|
A | G | 6 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0084others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320-1567A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045075 | ||||||
chr4:88045083
|
A | G | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1320-1559A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045083 | ||||||
chr4:88045159
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0046others(41): Show | 47 | HG00609.hp1 HG01109.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.1320-1483A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045159 | ||||||
chr4:88045348
|
A | G | 2 | a0005c0008t0001g0224a0005c0008t0003g0225 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1320-1294A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045348 | ||||||
chr4:88045649
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1320-993C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045649 | ||||||
chr4:88045763
|
A | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0102others(17): Show | 24 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.1320-879A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045763 | ||||||
chr4:88045767
|
A | G | 2 | a0001c0002t0002g0149a0001c0002t0002g0175 | 2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.1320-875A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045767 | ||||||
chr4:88045784
|
T | TA | 44 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(41): Show | 49 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1320-857dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr4 | 88045784 | |||||
chr4:88045856
|
A | G | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1320-786A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88045856 | ||||||
chr4:88046372
|
C | T | 1 | a0001c0002t0001g0183 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1320-270C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88046372 | ||||||
chr4:88046409
|
A | T | 1 | a0001c0001t0002g0053 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1320-233A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88046409 | ||||||
chr4:88046446
|
A | T | 3 | a0001c0001t0001g0228a0001c0009t0001g0229a0003c0004t0001g0030 | 3 | HG00639.hp1 HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1320-196A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | chr4 | 88046446 | ||||||
chr4:88046606
|
GTTGTTA | G | 4 | a0001c0010t0004g0100a0001c0010t0004g0101a0003c0007t0004g0020others(1): Show | 4 | HG01167.hp1 HG01192.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1320-30_1320-25del others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr4 | 88046606 | |||||
chr4:88047112
|
T | C | 3 | a0001c0001t0001g0228a0001c0009t0001g0229a0003c0004t0001g0030 | 3 | HG00639.hp1 HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1548+242T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047112 | ||||||
chr4:88047175
|
G | GT | 90 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(87): Show | 97 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1548+314dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 88047175 | |||||
chr4:88047191
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(88): Show | 98 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.1548+321A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047191 | ||||||
chr4:88047336
|
C | T | 55 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(52): Show | 75 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1548+466C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047336 | ||||||
chr4:88047561
|
A | G | 153 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(150): Show | 180 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.1548+691A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047561 | ||||||
chr4:88047602
|
G | A | 11 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1548+732G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047602 | ||||||
chr4:88047629
|
T | G | 1 | a0001c0002t0002g0145 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1548+759T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047629 | ||||||
chr4:88047697
|
G | T | 3 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1548+827G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047697 | ||||||
chr4:88047891
|
T | C | 3 | a0001c0001t0001g0244a0002c0003t0001g0085a0002c0003t0001g0086 | 3 | NA18972.hp2 NA18980.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1548+1021T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047891 | ||||||
chr4:88047954
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0268others(1): Show | 4 | NA18962.hp2 NA19003.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548+1084C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88047954 | ||||||
chr4:88048039
|
C | T | 5 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(2): Show | 5 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548+1169C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048039 | ||||||
chr4:88048367
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1548+1497T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048367 | ||||||
chr4:88048388
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1548+1518A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048388 | ||||||
chr4:88048593
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1548+1723C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048593 | ||||||
chr4:88048700
|
T | A | 1 | a0002c0003t0001g0075 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1548+1830T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048700 | ||||||
chr4:88048735
|
C | T | 3 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1548+1865C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048735 | ||||||
chr4:88048797
|
G | A | 1 | a0001c0001t0003g0301 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1548+1927G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048797 | ||||||
chr4:88048848
|
A | C | 1 | a0003c0004t0005g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1548+1978A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048848 | ||||||
chr4:88048904
|
C | T | 5 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(2): Show | 5 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548+2034C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88048904 | ||||||
chr4:88049223
|
C | T | 57 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(54): Show | 77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1548+2353C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049223 | ||||||
chr4:88049270
|
A | G | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1548+2400A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049270 | ||||||
chr4:88049375
|
G | A | 1 | a0003c0004t0004g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1548+2505G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049375 | ||||||
chr4:88049608
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0102others(16): Show | 23 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1549-2383G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049608 | ||||||
chr4:88049700
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1549-2291C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049700 | ||||||
chr4:88049784
|
A | C | 1 | a0001c0001t0001g0276 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1549-2207A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049784 | ||||||
chr4:88049818
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1549-2173A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049818 | ||||||
chr4:88049923
|
T | C | 2 | a0002c0003t0003g0135a0002c0003t0003g0136 | 2 | NA18952.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1549-2068T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88049923 | ||||||
chr4:88049969
|
A | AT | 11 | a0001c0001t0001g0057a0001c0001t0001g0233a0001c0001t0001g0284others(8): Show | 11 | HG01175.hp2 HG01243.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1549-1999dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 88049969 | |||||
chr4:88049969
|
AT | A | 53 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0131others(50): Show | 55 | HG00597.hp2 HG00639.hp1 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1549-1999delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 88049969 | |||||
chr4:88049969
|
ATT | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(38): Show | 46 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1549-2000_1549-199 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 88049969 | |||||
chr4:88050028
|
A | G | 154 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(151): Show | 181 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.1549-1963A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050028 | ||||||
chr4:88050175
|
C | T | 58 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(55): Show | 78 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1549-1816C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050175 | ||||||
chr4:88050260
|
C | G | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1549-1731C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050260 | ||||||
chr4:88050279
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1549-1712A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050279 | ||||||
chr4:88050295
|
G | A | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1549-1696G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050295 | ||||||
chr4:88050717
|
CA | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0102others(16): Show | 23 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1549-1273delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050717 | ||||||
chr4:88050781
|
A | G | 2 | a0005c0008t0001g0224a0005c0008t0003g0225 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1549-1210A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050781 | ||||||
chr4:88050899
|
G | A | 151 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(148): Show | 178 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(175): Show |
intron_variant | MODIFIER | c.1549-1092G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050899 | ||||||
chr4:88050900
|
T | C | 2 | a0002c0003t0003g0062a0002c0003t0003g0063 | 2 | NA18959.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1549-1091T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050900 | ||||||
chr4:88050915
|
T | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(176): Show | 207 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.1549-1076T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050915 | ||||||
chr4:88050983
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1549-1008G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88050983 | ||||||
chr4:88051514
|
A | C | 3 | a0001c0002t0001g0146a0001c0002t0001g0181a0002c0003t0001g0035 | 3 | HG01109.hp2 HG02148.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1549-477A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88051514 | ||||||
chr4:88051837
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1549-154A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88051837 | ||||||
chr4:88051854
|
T | C | 62 | a0001c0001t0001g0133a0001c0001t0001g0244a0001c0001t0002g0052others(59): Show | 83 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1549-137T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88051854 | ||||||
chr4:88051874
|
G | C | 8 | a0003c0004t0005g0019a0003c0004t0005g0023a0003c0004t0005g0025others(5): Show | 8 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1549-117G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88051874 | ||||||
chr4:88051944
|
C | T | 10 | a0001c0001t0004g0106a0001c0001t0004g0140a0003c0004t0005g0019others(7): Show | 10 | HG01109.hp1 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1549-47C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 6/14 | chr4 | 88051944 | ||||||
chr4:88052275
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(152): Show | 182 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.1716+117A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88052275 | ||||||
chr4:88052292
|
AG | A | 25 | a0001c0001t0004g0106a0001c0001t0004g0140a0001c0001t0004g0241others(22): Show | 26 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.1716+137delG | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88052292 | |||||
chr4:88052430
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1716+272G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88052430 | ||||||
chr4:88052468
|
T | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(152): Show | 182 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.1716+310T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88052468 | ||||||
chr4:88052487
|
T | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(152): Show | 182 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.1716+329T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88052487 | ||||||
chr4:88052878
|
A | C | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1716+720A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88052878 | ||||||
chr4:88053014
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0227a0001c0001t0006g0219others(1): Show | 4 | HG02738.hp2 HG03831.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+856C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053014 | ||||||
chr4:88053047
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1716+889A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053047 | ||||||
chr4:88053220
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1716+1062A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053220 | ||||||
chr4:88053228
|
T | C | 1 | a0002c0003t0001g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1716+1070T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053228 | ||||||
chr4:88053408
|
T | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(149): Show | 179 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.1716+1250T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053408 | ||||||
chr4:88053451
|
G | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716+1293G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053451 | ||||||
chr4:88053465
|
T | C | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1716+1307T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053465 | ||||||
chr4:88053469
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1716+1311C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053469 | ||||||
chr4:88053611
|
C | T | 1 | a0002c0003t0001g0006 | 2 | HG02083.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1716+1453C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053611 | ||||||
chr4:88053656
|
C | CA | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0121others(5): Show | 8 | HG00642.hp2 HG01361.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1716+1514dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88053656 | |||||
chr4:88053656
|
CA | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(138): Show | 169 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.1716+1514delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88053656 | |||||
chr4:88053936
|
T | C | 2 | a0001c0001t0007g0220a0001c0022t0001g0304 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1716+1778T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88053936 | ||||||
chr4:88054067
|
T | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(138): Show | 168 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.1716+1909T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054067 | ||||||
chr4:88054071
|
A | ATAATAAT others(11): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0117 | 4 | HG02055.hp1 HG02109.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+1948_1717-196 others(22): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88054071 | |||||
chr4:88054100
|
C | A | 1 | a0002c0003t0003g0042 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1716+1942C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054100 | ||||||
chr4:88054167
|
G | A | 1 | a0002c0003t0003g0311 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1717-1919G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054167 | ||||||
chr4:88054296
|
G | A | 1 | a0002c0003t0003g0311 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1717-1790G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054296 | ||||||
chr4:88054401
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1717-1685A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054401 | ||||||
chr4:88054532
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(50): Show | 58 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1717-1554G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054532 | ||||||
chr4:88054551
|
T | C | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1717-1535T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054551 | ||||||
chr4:88054586
|
T | C | 52 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(49): Show | 72 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1717-1500T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054586 | ||||||
chr4:88054650
|
C | CT | 102 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(99): Show | 109 | HG00597.hp2 HG00609.hp1 HG00733.hp2 others(106): Show |
intron_variant | MODIFIER | c.1717-1414dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88054650 | |||||
chr4:88054650
|
C | CTT | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0133others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1717-1415_1717-141 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88054650 | |||||
chr4:88054650
|
CT | C | 19 | a0001c0001t0004g0196a0001c0001t0004g0197a0001c0001t0004g0241others(16): Show | 20 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1717-1414delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88054650 | |||||
chr4:88054694
|
G | A | 3 | a0001c0001t0009g0110a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01934.hp2 HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1717-1392G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054694 | ||||||
chr4:88054817
|
G | T | 1 | a0003c0004t0004g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1717-1269G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054817 | ||||||
chr4:88054856
|
G | A | 50 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(47): Show | 70 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1717-1230G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054856 | ||||||
chr4:88054873
|
C | T | 1 | a0001c0002t0002g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1717-1213C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054873 | ||||||
chr4:88054945
|
C | T | 5 | a0001c0001t0004g0241a0003c0004t0004g0199a0003c0004t0004g0200others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-1141C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88054945 | ||||||
chr4:88055015
|
A | G | 1 | a0001c0001t0009g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1717-1071A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055015 | ||||||
chr4:88055099
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1717-987T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055099 | ||||||
chr4:88055105
|
A | G | 1 | a0001c0001t0004g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1717-981A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055105 | ||||||
chr4:88055412
|
C | T | 31 | a0001c0001t0004g0106a0001c0001t0004g0140a0001c0001t0004g0196others(28): Show | 32 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1717-674C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055412 | ||||||
chr4:88055441
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(139): Show | 169 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.1717-645A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055441 | ||||||
chr4:88055587
|
C | T | 2 | a0001c0001t0003g0301a0002c0003t0003g0056 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1717-499C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055587 | ||||||
chr4:88055638
|
CT | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0057others(124): Show | 151 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.1717-431delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88055638 | |||||
chr4:88055638
|
CTT | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0093others(13): Show | 19 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1717-432_1717-431d others(4): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 88055638 | |||||
chr4:88055746
|
C | T | 1 | a0003c0004t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1717-340C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 7/14 | chr4 | 88055746 | ||||||
chr4:88056770
|
A | G | 1 | a0001c0001t0009g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1898+503A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88056770 | ||||||
chr4:88056982
|
G | GT | 18 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0093others(15): Show | 22 | HG00733.hp2 HG00735.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1898+724dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 88056982 | |||||
chr4:88056987
|
T | G | 52 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(49): Show | 72 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1898+720T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88056987 | ||||||
chr4:88057250
|
A | G | 1 | a0001c0002t0002g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1899-733A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88057250 | ||||||
chr4:88057303
|
T | C | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1899-680T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88057303 | ||||||
chr4:88057436
|
C | CT | 9 | a0001c0002t0001g0156a0001c0002t0001g0158a0001c0002t0001g0176others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1899-530dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 88057436 | |||||
chr4:88057436
|
CT | C | 6 | a0001c0001t0001g0242a0001c0002t0001g0168a0001c0002t0002g0177others(3): Show | 6 | HG01167.hp1 HG02040.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.1899-530delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 88057436 | |||||
chr4:88057486
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1899-497A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88057486 | ||||||
chr4:88057515
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0008g0096 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1899-468A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88057515 | ||||||
chr4:88057713
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1899-270C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 8/14 | chr4 | 88057713 | ||||||
chr4:88058332
|
A | G | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2019+229A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88058332 | ||||||
chr4:88058377
|
C | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(138): Show | 168 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.2019+274C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88058377 | ||||||
chr4:88058536
|
CTCTTTCT | C | 3 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2019+439_2019+445d others(9): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88058536 | |||||
chr4:88058542
|
C | T | 6 | a0001c0001t0001g0118a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG00099.hp2 HG01256.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2019+439C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88058542 | ||||||
chr4:88058549
|
T | C | 1 | a0002c0003t0003g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2019+446T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88058549 | ||||||
chr4:88058738
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(50): Show | 58 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.2019+635G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88058738 | ||||||
chr4:88059294
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2019+1191C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059294 | ||||||
chr4:88059744
|
C | T | 2 | a0001c0002t0001g0176a0001c0022t0001g0304 | 2 | HG02145.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2019+1641C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059744 | ||||||
chr4:88059745
|
G | A | 1 | a0003c0015t0003g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2019+1642G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059745 | ||||||
chr4:88059745
|
G | GTACA | 92 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0046others(89): Show | 97 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(94): Show |
intron_variant | MODIFIER | c.2019+1677_2019+168 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88059745 | |||||
chr4:88059745
|
G | GTACATAC others(1): Show |
55 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0127others(52): Show | 75 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2019+1673_2019+168 others(12): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88059745 | |||||
chr4:88059745
|
G | GTACATAC others(5): Show |
4 | a0001c0001t0001g0109a0001c0001t0008g0096a0001c0002t0002g0172others(1): Show | 4 | HG01346.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+1669_2019+168 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88059745 | |||||
chr4:88059876
|
G | A | 3 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2019+1773G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059876 | ||||||
chr4:88059900
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2019+1797C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059900 | ||||||
chr4:88059972
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2019+1869A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88059972 | ||||||
chr4:88060130
|
G | A | 1 | a0002c0003t0001g0075 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2020-1776G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060130 | ||||||
chr4:88060178
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2020-1728C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060178 | ||||||
chr4:88060270
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0006g0219a0003c0004t0001g0210 | 3 | HG02738.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2020-1636T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060270 | ||||||
chr4:88060385
|
G | A | 30 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249others(27): Show | 32 | HG00597.hp2 HG01516.hp1 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.2020-1521G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060385 | ||||||
chr4:88060441
|
C | CAT | 4 | a0001c0001t0001g0228a0001c0001t0001g0283a0001c0001t0007g0220others(1): Show | 4 | HG00639.hp1 HG01243.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020-1450_2020-144 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATAT | 5 | a0001c0001t0001g0109a0001c0012t0003g0111a0001c0012t0003g0142others(2): Show | 5 | HG01167.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2020-1452_2020-144 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATAT | 78 | a0001c0001t0001g0044a0001c0001t0001g0057a0001c0001t0001g0064others(75): Show | 99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2020-1454_2020-144 others(10): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(1): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0093others(19): Show | 25 | HG00733.hp2 HG00735.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2020-1456_2020-144 others(12): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(3): Show |
5 | a0001c0006t0001g0018a0001c0006t0001g0217a0001c0006t0001g0218others(2): Show | 6 | HG01255.hp1 HG01884.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2020-1458_2020-144 others(14): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(7): Show |
5 | a0002c0003t0003g0037a0002c0003t0003g0063a0002c0003t0003g0067others(2): Show | 5 | HG01516.hp1 NA18941.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2020-1462_2020-144 others(18): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(9): Show |
12 | a0001c0001t0003g0239a0002c0003t0001g0039a0002c0003t0003g0003others(9): Show | 14 | HG01928.hp1 HG01952.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.2020-1464_2020-144 others(20): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(11): Show |
8 | a0001c0001t0003g0249a0001c0001t0003g0258a0002c0003t0003g0058others(5): Show | 8 | HG02015.hp1 NA18612.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2020-1449_2020-144 others(22): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(13): Show |
2 | a0001c0001t0003g0301a0002c0003t0003g0069 | 2 | HG00597.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2020-1449_2020-144 others(24): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(15): Show |
1 | a0001c0001t0003g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2020-1449_2020-144 others(26): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(17): Show |
1 | a0002c0003t0003g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2020-1449_2020-144 others(28): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060441
|
C | CATATATA others(19): Show |
1 | a0002c0003t0003g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2020-1449_2020-144 others(30): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88060441 | |||||
chr4:88060450
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2020-1456A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060450 | ||||||
chr4:88060516
|
G | C | 1 | a0001c0012t0003g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2020-1390G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060516 | ||||||
chr4:88060538
|
T | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(140): Show | 170 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2020-1368T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060538 | ||||||
chr4:88060603
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2020-1303C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060603 | ||||||
chr4:88060685
|
A | G | 30 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249others(27): Show | 32 | HG00597.hp2 HG01516.hp1 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.2020-1221A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060685 | ||||||
chr4:88060710
|
C | T | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2020-1196C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060710 | ||||||
chr4:88060976
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2020-930A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88060976 | ||||||
chr4:88061163
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2020-743G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061163 | ||||||
chr4:88061222
|
A | G | 1 | a0001c0001t0008g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2020-684A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061222 | ||||||
chr4:88061309
|
A | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(140): Show | 170 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2020-597A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061309 | ||||||
chr4:88061509
|
G | A | 1 | a0001c0001t0009g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2020-397G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061509 | ||||||
chr4:88061601
|
A | G | 1 | a0002c0003t0003g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2020-305A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061601 | ||||||
chr4:88061695
|
G | A | 1 | a0001c0001t0004g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2020-211G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061695 | ||||||
chr4:88061737
|
C | CA | 31 | a0001c0001t0001g0230a0001c0001t0001g0240a0001c0001t0003g0239others(28): Show | 33 | HG01516.hp1 HG01928.hp1 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.2020-158dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88061737 | |||||
chr4:88061737
|
CA | C | 54 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(51): Show | 74 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.2020-158delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 88061737 | |||||
chr4:88061748
|
A | T | 2 | a0001c0001t0007g0220a0001c0012t0003g0142 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2020-158A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061748 | ||||||
chr4:88061838
|
T | G | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2020-68T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 9/14 | chr4 | 88061838 | ||||||
chr4:88062183
|
A | C | 1 | a0001c0001t0001g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2118+179A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88062183 | ||||||
chr4:88062248
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0260 | 2 | NA18957.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2118+244A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88062248 | ||||||
chr4:88062344
|
A | G | 1 | a0001c0009t0001g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2118+340A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88062344 | ||||||
chr4:88062478
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2118+474A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88062478 | ||||||
chr4:88062503
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2118+499C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88062503 | ||||||
chr4:88062729
|
AT | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0099a0002c0003t0001g0060others(3): Show | 6 | HG00609.hp1 HG01255.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2118+736delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88062729 | |||||
chr4:88063166
|
A | G | 1 | a0002c0003t0001g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2118+1162A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063166 | ||||||
chr4:88063174
|
CACAA | C | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2118+1176_2118+117 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88063174 | |||||
chr4:88063185
|
A | C | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2118+1181A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063185 | ||||||
chr4:88063307
|
G | A | 1 | a0009c0018t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2118+1303G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063307 | ||||||
chr4:88063330
|
G | A | 2 | a0001c0002t0001g0183a0001c0002t0001g0194 | 2 | NA18961.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2118+1326G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063330 | ||||||
chr4:88063396
|
C | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(139): Show | 169 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2118+1392C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063396 | ||||||
chr4:88063446
|
G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0227a0001c0001t0006g0219others(1): Show | 4 | HG02738.hp2 HG03831.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118+1442G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063446 | ||||||
chr4:88063527
|
G | A | 1 | a0001c0002t0002g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2118+1523G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063527 | ||||||
chr4:88063531
|
C | CA | 44 | a0001c0001t0002g0052a0001c0001t0002g0120a0001c0002t0002g0001others(41): Show | 64 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.2118+1539dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88063531 | |||||
chr4:88063628
|
T | C | 1 | a0002c0003t0001g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2118+1624T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063628 | ||||||
chr4:88063805
|
C | CTTCACAT others(24): Show |
1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2119-1562_2119-153 others(35): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88063805 | |||||
chr4:88063815
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2119-1559A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063815 | ||||||
chr4:88063893
|
T | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(51): Show | 59 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119-1481T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063893 | ||||||
chr4:88063929
|
T | TA | 3 | a0001c0001t0001g0261a0001c0001t0001g0295a0001c0002t0001g0156 | 3 | NA18970.hp1 NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2119-1445_2119-144 others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88063929 | ||||||
chr4:88064000
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119-1374C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064000 | ||||||
chr4:88064052
|
G | A | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2119-1322G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064052 | ||||||
chr4:88064442
|
G | T | 1 | a0001c0001t0001g0280 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2119-932G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064442 | ||||||
chr4:88064504
|
C | G | 3 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024 | 3 | HG01167.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2119-870C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064504 | ||||||
chr4:88064559
|
G | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(134): Show | 164 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.2119-815G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064559 | ||||||
chr4:88064607
|
C | G | 3 | a0001c0001t0001g0228a0001c0013t0003g0034a0003c0004t0001g0030 | 3 | HG00639.hp1 HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2119-767C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064607 | ||||||
chr4:88064728
|
C | CA | 8 | a0001c0001t0001g0141a0001c0001t0001g0242a0001c0001t0001g0255others(5): Show | 8 | HG02040.hp1 HG02040.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2119-633dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88064728 | |||||
chr4:88064814
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119-560C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064814 | ||||||
chr4:88064849
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119-525G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064849 | ||||||
chr4:88064930
|
TTTTG | T | 51 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(48): Show | 71 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2119-424_2119-421d others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 88064930 | |||||
chr4:88064940
|
T | G | 1 | a0008c0023t0003g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2119-434T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88064940 | ||||||
chr4:88065010
|
C | G | 1 | a0001c0001t0004g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2119-364C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88065010 | ||||||
chr4:88065206
|
T | C | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2119-168T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88065206 | ||||||
chr4:88065243
|
A | G | 2 | a0006c0011t0002g0094a0006c0011t0002g0095 | 2 | HG01981.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2119-131A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 10/14 | chr4 | 88065243 | ||||||
chr4:88065593
|
C | CT | 62 | a0001c0001t0001g0112a0001c0001t0001g0228a0001c0001t0001g0240others(59): Show | 82 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.2240+113dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr4 | 88065593 | |||||
chr4:88065593
|
CT | C | 18 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0083others(15): Show | 19 | HG00609.hp1 HG01167.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.2240+113delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr4 | 88065593 | |||||
chr4:88065609
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0282a0001c0001t0001g0303 | 3 | HG00099.hp1 HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2240+114C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 11/14 | chr4 | 88065609 | ||||||
chr4:88065902
|
G | A | 4 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(1): Show | 4 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2358+23G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88065902 | ||||||
chr4:88065966
|
A | G | 1 | a0001c0001t0007g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2358+87A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88065966 | ||||||
chr4:88066116
|
A | G | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2358+237A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066116 | ||||||
chr4:88066124
|
A | T | 31 | a0001c0001t0004g0106a0001c0001t0004g0140a0001c0001t0004g0196others(28): Show | 32 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.2358+245A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066124 | ||||||
chr4:88066167
|
T | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2358+288T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066167 | ||||||
chr4:88066169
|
A | G | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2358+290A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066169 | ||||||
chr4:88066266
|
A | G | 2 | a0001c0001t0001g0228a0003c0004t0001g0030 | 2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2358+387A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066266 | ||||||
chr4:88066363
|
C | CT | 6 | a0001c0001t0001g0247a0001c0001t0001g0255a0001c0002t0001g0158others(3): Show | 6 | HG00558.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2358+500dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 88066363 | |||||
chr4:88066363
|
CTTTTTTT others(2): Show |
C | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(46): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2358+492_2358+500d others(11): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 88066363 | |||||
chr4:88066369
|
T | C | 2 | a0003c0004t0004g0204a0003c0004t0004g0208 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2358+490T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066369 | ||||||
chr4:88066402
|
C | G | 33 | a0001c0001t0002g0052a0001c0002t0002g0001a0001c0002t0002g0002others(30): Show | 50 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2358+523C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066402 | ||||||
chr4:88066428
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2358+549C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066428 | ||||||
chr4:88066751
|
GA | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0093others(13): Show | 20 | HG00733.hp2 HG00735.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2358+881delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 88066751 | |||||
chr4:88066763
|
C | T | 30 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249others(27): Show | 32 | HG00597.hp2 HG01516.hp1 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.2358+884C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066763 | ||||||
chr4:88066764
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(139): Show | 169 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2358+885A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066764 | ||||||
chr4:88066979
|
G | A | 1 | a0002c0003t0001g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2359-919G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88066979 | ||||||
chr4:88067039
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2359-859A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88067039 | ||||||
chr4:88067441
|
A | G | 12 | a0001c0001t0001g0232a0001c0001t0001g0253a0001c0001t0001g0255others(9): Show | 12 | HG00438.hp1 HG01346.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.2359-457A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88067441 | ||||||
chr4:88067511
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2359-387T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88067511 | ||||||
chr4:88067713
|
C | A | 1 | a0007c0014t0003g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2359-185C>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 12/14 | chr4 | 88067713 | ||||||
chr4:88068212
|
T | C | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2522+151T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88068212 | ||||||
chr4:88068437
|
A | T | 2 | a0006c0011t0002g0094a0006c0011t0002g0095 | 2 | HG01981.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2522+376A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88068437 | ||||||
chr4:88068448
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2522+387C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88068448 | ||||||
chr4:88068463
|
C | G | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2522+402C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88068463 | ||||||
chr4:88068469
|
CA | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(136): Show | 166 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.2522+421delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88068469 | |||||
chr4:88068850
|
C | T | 1 | a0003c0007t0004g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2522+789C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88068850 | ||||||
chr4:88069234
|
T | G | 29 | a0001c0001t0003g0239a0001c0001t0003g0248a0001c0001t0003g0249others(26): Show | 31 | HG00597.hp2 HG01516.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.2522+1173T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069234 | ||||||
chr4:88069505
|
T | G | 1 | a0001c0001t0008g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2522+1444T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069505 | ||||||
chr4:88069564
|
C | T | 1 | a0001c0002t0002g0012 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2522+1503C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069564 | ||||||
chr4:88069602
|
A | G | 1 | a0002c0003t0001g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2522+1541A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069602 | ||||||
chr4:88069828
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2522+1767G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069828 | ||||||
chr4:88069871
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2522+1810A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88069871 | ||||||
chr4:88070077
|
T | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0300others(1): Show | 4 | HG01433.hp1 HG01952.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522+2016T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070077 | ||||||
chr4:88070226
|
C | T | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2522+2165C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070226 | ||||||
chr4:88070329
|
A | G | 1 | a0001c0001t0008g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2522+2268A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070329 | ||||||
chr4:88070384
|
A | G | 1 | a0001c0022t0001g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2522+2323A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070384 | ||||||
chr4:88070435
|
G | A | 1 | a0001c0002t0002g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2522+2374G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070435 | ||||||
chr4:88070571
|
A | T | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2522+2510A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070571 | ||||||
chr4:88070572
|
T | A | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2522+2511T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070572 | ||||||
chr4:88070574
|
T | A | 3 | a0003c0004t0004g0017a0007c0014t0003g0198a0008c0023t0003g0302 | 4 | HG01255.hp1 HG01257.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2522+2513T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070574 | ||||||
chr4:88070574
|
TTA | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0082others(15): Show | 22 | HG00733.hp2 HG00735.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.2522+2540_2522+254 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070574 | |||||
chr4:88070574
|
TTATA | T | 15 | a0001c0001t0001g0044a0001c0001t0001g0064a0001c0001t0001g0084others(12): Show | 15 | HG00597.hp2 HG02145.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2522+2538_2522+254 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070574 | |||||
chr4:88070574
|
TTATATA | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0195a0001c0001t0015g0143 | 3 | HG03130.hp1 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2522+2536_2522+254 others(10): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070574 | |||||
chr4:88070574
|
TTATATAT others(5): Show |
T | 2 | a0001c0001t0001g0057a0001c0001t0001g0119 | 2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2522+2530_2522+254 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070574 | |||||
chr4:88070575
|
T | A | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(46): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2522+2514T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070575 | ||||||
chr4:88070576
|
A | T | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(46): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2522+2515A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070576 | ||||||
chr4:88070578
|
A | T | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(46): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2522+2517A>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070578 | ||||||
chr4:88070589
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0228a0001c0002t0002g0192 | 2 | HG00639.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2522+2530_2522+254 others(18): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070589 | |||||
chr4:88070591
|
T | G | 2 | a0001c0001t0001g0098a0001c0001t0006g0219 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2522+2530T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070591 | ||||||
chr4:88070591
|
TATATATA others(7): Show |
T | 37 | a0001c0001t0002g0052a0001c0001t0002g0120a0001c0002t0002g0001others(34): Show | 54 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2522+2532_2522+254 others(18): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070591 | |||||
chr4:88070593
|
T | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0084others(12): Show | 16 | HG02040.hp2 HG02109.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.2522+2532T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070593 | ||||||
chr4:88070593
|
T | TAG | 4 | a0001c0001t0001g0046a0001c0001t0001g0114a0001c0001t0001g0234others(1): Show | 4 | HG00099.hp2 HG01978.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522+2533_2522+253 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070593 | |||||
chr4:88070593
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2522+2534_2522+254 others(14): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070593 | |||||
chr4:88070593
|
TATATATA others(7): Show |
T | 12 | a0001c0001t0002g0053a0001c0001t0007g0220a0001c0002t0002g0012others(9): Show | 15 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.2522+2534_2522+254 others(18): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070593 | |||||
chr4:88070595
|
T | G | 46 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0066others(43): Show | 47 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.2522+2534T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070595 | ||||||
chr4:88070595
|
T | TAG | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0105others(8): Show | 11 | HG01081.hp1 HG02293.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.2522+2535_2522+253 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070595 | |||||
chr4:88070595
|
TATATATA others(7): Show |
T | 1 | a0001c0002t0002g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2522+2536_2522+254 others(18): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070595 | |||||
chr4:88070597
|
T | G | 108 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0048others(105): Show | 109 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.2522+2536T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070597 | ||||||
chr4:88070597
|
T | TAG | 14 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0090others(11): Show | 14 | HG01433.hp1 HG01952.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.2522+2537_2522+253 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070597 | |||||
chr4:88070597
|
T | TAGAG | 3 | a0001c0001t0001g0240a0003c0004t0001g0203a0005c0008t0003g0225 | 3 | HG02572.hp1 NA18967.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2522+2537_2522+253 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070597 | |||||
chr4:88070599
|
T | G | 163 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0045others(160): Show | 168 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.2522+2538T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070599 | ||||||
chr4:88070599
|
T | TAG | 10 | a0001c0001t0001g0310a0001c0001t0010g0221a0001c0001t0013g0264others(7): Show | 10 | HG02015.hp1 HG02148.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.2522+2539_2522+254 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070599 | |||||
chr4:88070599
|
T | TAGAG | 9 | a0001c0001t0001g0227a0001c0001t0001g0244a0001c0002t0001g0157others(6): Show | 9 | HG00323.hp2 HG01192.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2522+2539_2522+254 others(8): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070599 | |||||
chr4:88070599
|
T | TAGAGAGA others(1): Show |
3 | a0003c0004t0004g0199a0003c0004t0004g0214a0003c0004t0005g0023 | 3 | HG01175.hp1 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2522+2539_2522+254 others(12): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070599 | |||||
chr4:88070601
|
T | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0044others(205): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2522+2540T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070601 | ||||||
chr4:88070601
|
T | TAG | 6 | a0001c0001t0001g0112a0001c0001t0001g0295a0001c0001t0001g0306others(3): Show | 6 | HG02083.hp1 HG03239.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2522+2566_2522+256 others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TAGAGAG | 4 | a0003c0004t0004g0201a0003c0004t0004g0205a0003c0004t0004g0216others(1): Show | 4 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2522+2562_2522+256 others(10): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TAGAGAGA others(3): Show |
2 | a0003c0004t0004g0202a0003c0004t0005g0019 | 2 | HG02818.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2522+2558_2522+256 others(14): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATAGAGA others(5): Show |
2 | a0003c0004t0004g0206a0003c0007t0004g0020 | 2 | HG00642.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.2522+2541_2522+254 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATATAGA others(3): Show |
1 | a0001c0001t0004g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2522+2541_2522+254 others(14): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATATAGA others(5): Show |
3 | a0001c0010t0004g0100a0001c0010t0004g0101a0003c0004t0004g0207 | 3 | HG01123.hp2 HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2522+2541_2522+254 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATATATA others(3): Show |
1 | a0003c0004t0005g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2522+2541_2522+254 others(14): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATATATA others(5): Show |
2 | a0001c0001t0004g0197a0003c0004t0004g0213 | 2 | HG01361.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2522+2541_2522+254 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070601
|
T | TATATATA others(5): Show |
3 | a0001c0001t0004g0196a0003c0007t0004g0021a0003c0007t0004g0022 | 3 | HG01106.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2522+2541_2522+254 others(16): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070601 | |||||
chr4:88070603
|
G | T | 3 | a0001c0001t0001g0281a0003c0004t0005g0025a0003c0004t0005g0032 | 3 | HG02895.hp2 HG02897.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2522+2542G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070603 | ||||||
chr4:88070605
|
G | T | 2 | a0003c0004t0005g0025a0003c0004t0005g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2522+2544G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070605 | ||||||
chr4:88070628
|
A | AG | 3 | a0001c0001t0001g0238a0001c0001t0001g0265a0004c0005t0001g0043 | 3 | HG00438.hp1 HG01433.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2522+2567_2522+256 others(5): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070628 | ||||||
chr4:88070746
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2522+2685C>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070746 | ||||||
chr4:88070803
|
T | A | 4 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(1): Show | 4 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2522+2742T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070803 | ||||||
chr4:88070803
|
T | TA | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(46): Show | 69 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2522+2751dupA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88070803 | |||||
chr4:88070816
|
G | T | 1 | a0001c0001t0001g0232 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2522+2755G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070816 | ||||||
chr4:88070830
|
T | C | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2522+2769T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070830 | ||||||
chr4:88070836
|
T | C | 1 | a0002c0003t0003g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2522+2775T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070836 | ||||||
chr4:88070886
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2522+2825C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070886 | ||||||
chr4:88070924
|
C | T | 2 | a0003c0004t0004g0204a0003c0004t0004g0208 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2522+2863C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070924 | ||||||
chr4:88070934
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2522+2873C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88070934 | ||||||
chr4:88071000
|
G | A | 1 | a0005c0008t0003g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2522+2939G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071000 | ||||||
chr4:88071061
|
C | CT | 47 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(44): Show | 52 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.2522+3010dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88071061 | |||||
chr4:88071076
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2522+3015G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071076 | ||||||
chr4:88071189
|
G | A | 1 | a0003c0004t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2522+3128G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071189 | ||||||
chr4:88071497
|
T | C | 4 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(1): Show | 4 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2523-3315T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071497 | ||||||
chr4:88071561
|
TTTG | T | 3 | a0001c0001t0001g0084a0001c0001t0012g0222a0003c0004t0001g0031 | 3 | HG03041.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2523-3233_2523-323 others(7): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88071561 | |||||
chr4:88071661
|
T | G | 56 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0120others(53): Show | 76 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.2523-3151T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071661 | ||||||
chr4:88071736
|
G | A | 1 | a0001c0002t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2523-3076G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071736 | ||||||
chr4:88071817
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2523-2995T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88071817 | ||||||
chr4:88071975
|
C | CT | 32 | a0001c0001t0001g0048a0001c0001t0001g0082a0001c0001t0001g0123others(29): Show | 33 | HG00639.hp1 HG01106.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.2523-2812dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88071975 | |||||
chr4:88071975
|
CT | C | 46 | a0001c0001t0001g0083a0001c0001t0001g0277a0001c0001t0003g0239others(43): Show | 48 | HG00597.hp2 HG00642.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.2523-2812delT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88071975 | |||||
chr4:88072105
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2523-2707C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072105 | ||||||
chr4:88072275
|
G | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0268others(1): Show | 4 | NA18962.hp2 NA19003.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2523-2537G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072275 | ||||||
chr4:88072429
|
G | A | 1 | a0002c0003t0003g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2523-2383G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072429 | ||||||
chr4:88072429
|
G | C | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2523-2383G>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072429 | ||||||
chr4:88072693
|
A | G | 1 | a0001c0001t0008g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2523-2119A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072693 | ||||||
chr4:88072764
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0228a0001c0001t0007g0220others(1): Show | 4 | HG00639.hp1 HG01243.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2523-2048A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072764 | ||||||
chr4:88072903
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2523-1909G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072903 | ||||||
chr4:88072929
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523-1883G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88072929 | ||||||
chr4:88073034
|
CA | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(79): Show | 88 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.2523-1759delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88073034 | |||||
chr4:88073036
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0128 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2523-1776A>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073036 | ||||||
chr4:88073069
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0083others(11): Show | 15 | HG00609.hp1 HG02723.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.2523-1743G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073069 | ||||||
chr4:88073072
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2523-1740T>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073072 | ||||||
chr4:88073114
|
G | T | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2523-1698G>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073114 | ||||||
chr4:88073188
|
TA | T | 43 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0124others(40): Show | 46 | HG00597.hp2 HG01516.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.2523-1606delA | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88073188 | |||||
chr4:88073242
|
C | T | 1 | a0001c0001t0010g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2523-1570C>T | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073242 | ||||||
chr4:88073807
|
T | A | 1 | a0004c0005t0001g0252 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2523-1005T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073807 | ||||||
chr4:88073922
|
T | C | 2 | a0007c0014t0003g0198a0008c0023t0003g0302 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2523-890T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073922 | ||||||
chr4:88073982
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0006g0219a0003c0004t0001g0210 | 3 | HG02738.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2523-830G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88073982 | ||||||
chr4:88074137
|
TTTTG | T | 3 | a0001c0001t0001g0288a0001c0001t0001g0306a0001c0001t0001g0308 | 3 | NA19011.hp1 NA19058.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2523-659_2523-656d others(6): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88074137 | |||||
chr4:88074153
|
G | GT | 3 | a0001c0001t0001g0084a0001c0001t0012g0222a0003c0004t0001g0031 | 3 | HG03041.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2523-654dupT | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 88074153 | |||||
chr4:88074168
|
T | C | 4 | a0001c0012t0003g0111a0001c0012t0003g0142a0003c0015t0003g0024others(1): Show | 4 | HG01167.hp2 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2523-644T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074168 | ||||||
chr4:88074334
|
T | A | 1 | a0007c0014t0003g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2523-478T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074334 | ||||||
chr4:88074410
|
T | A | 3 | a0001c0001t0001g0228a0001c0001t0007g0220a0003c0004t0001g0030 | 3 | HG00639.hp1 HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2523-402T>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074410 | ||||||
chr4:88074418
|
G | A | 2 | a0001c0001t0001g0277a0003c0004t0001g0215 | 2 | HG01074.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2523-394G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074418 | ||||||
chr4:88074478
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2523-334G>A | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074478 | ||||||
chr4:88074643
|
T | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0044others(138): Show | 168 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.2523-169T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 13/14 | chr4 | 88074643 | ||||||
chr4:88075183
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2670+224T>C | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 14/14 | chr4 | 88075183 | ||||||
chr4:88075230
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2671-228A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 14/14 | chr4 | 88075230 | ||||||
chr4:88075249
|
AGGTGTTA others(27): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2671-208_2671-175d others(36): Show |
PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 14/14 | chr4 | 88075249 | ||||||
chr4:88075331
|
A | G | 1 | a0001c0002t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2671-127A>G | PKD2 | ENSG00000118762.8 | transcript | ENST00000237596.7 | protein_coding | 14/14 | chr4 | 88075331 |