geneid | 10016 |
---|---|
ensemblid | ENSG00000249915.9 |
hgncid | 8765 |
symbol | PDCD6 |
name | programmed cell death 6 |
refseq_nuc | NM_013232.4 |
refseq_prot | NP_037364.1 |
ensembl_nuc | ENST00000264933.9 |
ensembl_prot | ENSP00000264933.4 |
mane_status | MANE Select |
chr | chr5 |
start | 271646 |
end | 314974 |
strand | + |
ver | v1.2 |
region | chr5:271646-314974 |
region5000 | chr5:266646-319974 |
regionname0 | PDCD6_chr5_271646_314974 |
regionname5000 | PDCD6_chr5_266646_319974 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 191 | 316 | 62 | 66 | 138 | 13 | 35 | 99 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002 | 0/0 | 187 | 37 | 10 | 15 | 8 | 1 | 3 | 5 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0003 | 0/0 | 187 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 576 | 158 | 43 | 34 | 50 | 11 | 19 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
c0002 | 1/0 | 576 | 158 | 19 | 32 | 88 | 2 | 16 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
c0003 | 0/0 | 564 | 24 | 2 | 12 | 7 | 1 | 2 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
c0004 | 0/0 | 564 | 13 | 8 | 3 | 1 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
c0005 | 0/0 | 564 | 7 | 6 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 535 | 304 | 34 | 75 | 143 | 14 | 36 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0002 | 0/0 | 535 | 24 | 22 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0003 | 0/0 | 535 | 15 | 10 | 3 | 1 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0004 | 0/0 | 535 | 7 | 6 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0005 | 0/0 | 535 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0006 | 0/0 | 534 | 3 | 0 | 0 | 2 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
t0007 | 0/0 | 535 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 576 | 158 | 43 | 34 | 50 | 11 | 19 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0002 | 1/0 | 576 | 158 | 19 | 32 | 88 | 2 | 16 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0003 | 0/0 | 564 | 24 | 2 | 12 | 7 | 1 | 2 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0004 | 0/0 | 564 | 13 | 8 | 3 | 1 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0003c0005 | 0/0 | 564 | 7 | 6 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1110 | 123 | 13 | 32 | 48 | 11 | 18 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0001t0002 | 0/0 | 1110 | 23 | 21 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0001t0003 | 0/0 | 1110 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0001t0005 | 0/0 | 1110 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0001t0006 | 0/0 | 1109 | 3 | 0 | 0 | 2 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0001c0002t0001 | 1/0 | 1110 | 158 | 19 | 32 | 88 | 2 | 16 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0003t0001 | 0/0 | 1098 | 23 | 2 | 11 | 7 | 1 | 2 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0003t0007 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0004t0002 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0002c0004t0003 | 0/0 | 1098 | 12 | 7 | 3 | 1 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
a0003c0005t0004 | 0/0 | 1098 | 7 | 6 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | copy fasta | chr5 | 266646 | 319974 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0003t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0002c0004t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
a0003c0005t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | GBR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0291 | EUR | GBR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | FIN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0283 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00733 | hp2 | a0002 | c0003 | t0007 | g0287 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00735 | hp1 | a0002 | c0004 | t0003 | g0298 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01070 | hp2 | a0002 | c0003 | t0001 | g0297 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0288 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01081 | hp2 | a0002 | c0004 | t0003 | g0282 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01099 | hp2 | a0003 | c0005 | t0004 | g0306 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0327 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01169 | hp1 | a0002 | c0004 | t0003 | g0281 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0277 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0289 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01891 | hp2 | a0003 | c0005 | t0004 | g0308 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0294 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0296 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0293 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02004 | hp2 | a0002 | c0003 | t0001 | g0285 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0302 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0295 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02055 | hp2 | a0002 | c0004 | t0003 | g0276 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0300 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | CDX | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | CDX | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0278 | AMR | PEL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02451 | hp2 | a0002 | c0004 | t0003 | g0267 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02572 | hp2 | a0002 | c0004 | t0003 | g0279 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0286 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02886 | hp2 | a0003 | c0005 | t0004 | g0305 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03041 | hp2 | a0002 | c0004 | t0002 | g0269 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03130 | hp2 | a0003 | c0005 | t0004 | g0020 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03139 | hp2 | a0003 | c0005 | t0004 | g0307 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03209 | hp2 | a0003 | c0005 | t0004 | g0309 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03486 | hp2 | a0003 | c0005 | t0004 | g0020 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | ESN | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03669 | hp2 | a0002 | c0004 | t0003 | g0275 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0320 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0321 | SAS | PJL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0221 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0027 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | BEB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | CHB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | CHB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18906 | hp1 | a0002 | c0004 | t0003 | g0266 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18978 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19012 | hp2 | a0002 | c0004 | t0003 | g0280 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19030 | hp1 | a0002 | c0004 | t0003 | g0290 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0304 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA19240 | hp2 | a0002 | c0004 | t0003 | g0265 | AFR | YRI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ASW | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ASW | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0299 | AMR | CLM | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02486 | hp2 | a0002 | c0004 | t0003 | g0268 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | USA | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
HG06807 | hp2 | a0002 | c0003 | t0001 | g0274 | AFR | USA | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0292 | AFR | LWK | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0211 | REF | REF | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0088 | REF | REF | PDCD6_chr5_266646_319974 | PDCD6 | chr5 | 266646 | 319974 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:271728
|
C | G | 1 | a0003 | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
missense_variant | MODERATE | c.8C>G | p.Ala3Gly | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/6 | 83/1110 | 8/576 | 3/191 | chr5 | 271728 | ||
chr5:271742
|
CCCGGCCC others(5): Show |
C | 2 | a0002a0003 | 44 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(41): Show |
conservative_inframe_deletion | MODERATE | c.34_45delGCCGGCCCTG others(2): Show |
p.Ala12_Gly15del | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/6 | 109/1110 | 34/576 | 12/191 | INFO_REALIGN_3_PRIME | chr5 | 271742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:311363
|
T | C | 3 | a0001c0001a0002c0004a0003c0005 | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
synonymous_variant | LOW | c.438T>C | p.Ile146Ile | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/6 | 513/1110 | 438/576 | 146/191 | chr5 | 311363 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:271657
|
C | T | 1 | a0003c0005t0004 | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-64C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/6 | 64 | chr5 | 271657 | |||||
chr5:271672
|
A | C | 1 | a0002c0003t0007 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/6 | 49 | chr5 | 271672 | |||||
chr5:271703
|
A | G | 1 | a0003c0005t0004 | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-18A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/6 | 18 | chr5 | 271703 | |||||
chr5:314634
|
C | T | 1 | a0001c0001t0005 | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*119C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 6/6 | 119 | chr5 | 314634 | |||||
chr5:314820
|
T | C | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(3): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 6/6 | 305 | chr5 | 314820 | |||||
chr5:314903
|
CT | C | 1 | a0001c0001t0006 | 3 | HG03834.hp1 NA18941.hp1 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*394delT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 6/6 | 394 | INFO_REALIGN_3_PRIME | chr5 | 314903 | ||||
chr5:314958
|
G | A | 2 | a0001c0001t0002a0002c0004t0002 | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*443G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 6/6 | 443 | chr5 | 314958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:271928
|
TCCTCCGT others(24): Show |
T | 4 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 5 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+113_101+143del others(31): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 271928 | |||||
chr5:271997
|
A | G | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.101+176A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 271997 | ||||||
chr5:272046
|
C | T | 26 | a0001c0001t0001g0328a0001c0002t0001g0003a0001c0002t0001g0311others(23): Show | 28 | HG00609.hp2 HG01109.hp2 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.101+225C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272046 | ||||||
chr5:272107
|
CG | C | 67 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(64): Show | 71 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.101+289delG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 272107 | |||||
chr5:272113
|
C | A | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.101+292C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272113 | ||||||
chr5:272252
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(170): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.101+431C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272252 | ||||||
chr5:272257
|
G | GC | 173 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(170): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.101+437dupC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 272257 | |||||
chr5:272278
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.102-433C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272278 | ||||||
chr5:272330
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-381C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272330 | ||||||
chr5:272350
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102-361C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272350 | ||||||
chr5:272391
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.102-320C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272391 | ||||||
chr5:272423
|
G | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG00099.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-288G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272423 | ||||||
chr5:272447
|
G | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.102-264G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272447 | ||||||
chr5:272524
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102-187G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272524 | ||||||
chr5:272578
|
C | A | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-133C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272578 | ||||||
chr5:272579
|
C | G | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0159others(80): Show | 88 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.102-132C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272579 | ||||||
chr5:272645
|
A | G | 10 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 10 | HG00621.hp1 HG00639.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-66A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272645 | ||||||
chr5:272675
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.102-36C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 1/5 | chr5 | 272675 | ||||||
chr5:272791
|
A | C | 66 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(63): Show | 69 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.163+19A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272791 | ||||||
chr5:272801
|
C | T | 1 | a0001c0002t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.163+29C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272801 | ||||||
chr5:272816
|
C | T | 73 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0002g0008others(70): Show | 76 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.163+44C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272816 | ||||||
chr5:272895
|
T | A | 72 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(69): Show | 75 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.163+123T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272895 | ||||||
chr5:272905
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+133G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272905 | ||||||
chr5:272907
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+135A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272907 | ||||||
chr5:272974
|
C | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00438.hp1 HG01192.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+202C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 272974 | ||||||
chr5:273028
|
A | G | 72 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(69): Show | 75 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.163+256A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273028 | ||||||
chr5:273063
|
C | CTGTACAG others(71): Show |
6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+292_163+369dup others(78): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 273063 | |||||
chr5:273094
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.163+322A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273094 | ||||||
chr5:273204
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0001g0157 | 2 | HG02080.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.163+432A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273204 | ||||||
chr5:273211
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0157 | 2 | HG02080.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.163+439T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273211 | ||||||
chr5:273381
|
A | G | 10 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG02015.hp2 HG02132.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+609A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273381 | ||||||
chr5:273424
|
C | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(333): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.163+652C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273424 | ||||||
chr5:273438
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.163+666C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273438 | ||||||
chr5:273683
|
C | A | 1 | a0001c0002t0001g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163+911C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273683 | ||||||
chr5:273692
|
TG | T | 73 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(70): Show | 76 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.163+927delG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 273692 | |||||
chr5:273693
|
G | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+921G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273693 | ||||||
chr5:273696
|
G | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+924G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273696 | ||||||
chr5:273711
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+939G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273711 | ||||||
chr5:273789
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163+1017A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273789 | ||||||
chr5:273839
|
C | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+1067C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273839 | ||||||
chr5:273935
|
GT | G | 113 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.163+1177delT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 273935 | |||||
chr5:273935
|
GTTT | G | 70 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.163+1175_163+1177d others(5): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 273935 | |||||
chr5:273939
|
T | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+1167T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273939 | ||||||
chr5:273940
|
T | G | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1168T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273940 | ||||||
chr5:273966
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+1194G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273966 | ||||||
chr5:273970
|
T | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+1198T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273970 | ||||||
chr5:273990
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+1218G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273990 | ||||||
chr5:273995
|
T | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+1223T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 273995 | ||||||
chr5:274290
|
T | A | 1 | a0002c0003t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.163+1518T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274290 | ||||||
chr5:274485
|
T | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00597.hp2 NA18975.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.163+1713T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274485 | ||||||
chr5:274581
|
G | C | 1 | a0001c0002t0001g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+1809G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274581 | ||||||
chr5:274747
|
C | T | 1 | a0001c0002t0001g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.163+1975C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274747 | ||||||
chr5:274769
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+1997T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274769 | ||||||
chr5:274787
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.163+2015A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274787 | ||||||
chr5:274788
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.163+2016G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274788 | ||||||
chr5:274872
|
A | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG02602.hp1 HG02698.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+2100A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274872 | ||||||
chr5:274892
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+2120T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274892 | ||||||
chr5:274925
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.163+2153T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274925 | ||||||
chr5:274926
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.163+2154G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274926 | ||||||
chr5:274928
|
G | A | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+2156G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274928 | ||||||
chr5:274969
|
C | T | 5 | a0001c0002t0001g0013a0001c0002t0001g0091a0001c0002t0001g0145others(2): Show | 6 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+2197C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274969 | ||||||
chr5:274986
|
A | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(166): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.163+2214A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274986 | ||||||
chr5:274993
|
C | T | 1 | a0001c0001t0005g0272 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163+2221C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 274993 | ||||||
chr5:275002
|
C | T | 5 | a0001c0001t0001g0237a0001c0002t0001g0054a0001c0002t0001g0055others(2): Show | 5 | HG00621.hp2 HG02135.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2230C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275002 | ||||||
chr5:275019
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.163+2247C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275019 | ||||||
chr5:275020
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+2248A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275020 | ||||||
chr5:275026
|
C | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+2254C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275026 | ||||||
chr5:275062
|
CT | C | 179 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.163+2291delT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275062 | ||||||
chr5:275080
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.163+2308T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275080 | ||||||
chr5:275081
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.163+2309G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275081 | ||||||
chr5:275091
|
C | T | 6 | a0001c0001t0001g0159a0002c0004t0002g0269a0002c0004t0003g0265others(3): Show | 6 | HG01358.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+2319C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275091 | ||||||
chr5:275094
|
A | AC | 6 | a0001c0001t0001g0159a0002c0004t0002g0269a0002c0004t0003g0265others(3): Show | 6 | HG01358.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+2324dupC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 275094 | |||||
chr5:275173
|
C | T | 44 | a0001c0001t0001g0336a0001c0001t0001g0337a0002c0003t0001g0274others(41): Show | 45 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.163+2401C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275173 | ||||||
chr5:275187
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.163+2415G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275187 | ||||||
chr5:275365
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.163+2593C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275365 | ||||||
chr5:275388
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+2616G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275388 | ||||||
chr5:275477
|
G | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+2705G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275477 | ||||||
chr5:275548
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.163+2776T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275548 | ||||||
chr5:275755
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+2983C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275755 | ||||||
chr5:275810
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.163+3038A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275810 | ||||||
chr5:275870
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.163+3098G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275870 | ||||||
chr5:275887
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.163+3115C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275887 | ||||||
chr5:275953
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163+3181C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275953 | ||||||
chr5:275984
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+3212A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 275984 | ||||||
chr5:276075
|
A | G | 31 | a0001c0001t0001g0328a0001c0002t0001g0003a0001c0002t0001g0053others(28): Show | 33 | HG00609.hp2 HG01109.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.163+3303A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276075 | ||||||
chr5:276085
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3313T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276085 | ||||||
chr5:276113
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3341C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276113 | ||||||
chr5:276202
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3430C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276202 | ||||||
chr5:276250
|
G | A | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | NA18939.hp2 NA18973.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+3478G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276250 | ||||||
chr5:276353
|
A | G | 3 | a0001c0002t0001g0135a0001c0002t0001g0156a0001c0002t0001g0157 | 3 | NA18945.hp2 NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.163+3581A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276353 | ||||||
chr5:276368
|
GC | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0247others(1): Show | 4 | HG02071.hp1 NA18941.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+3597delC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276368 | ||||||
chr5:276395
|
G | C | 2 | a0001c0002t0001g0026a0002c0003t0001g0027 | 2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.163+3623G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276395 | ||||||
chr5:276509
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.163+3737C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276509 | ||||||
chr5:276521
|
A | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3749A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276521 | ||||||
chr5:276603
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3831T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276603 | ||||||
chr5:276966
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163+4194G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276966 | ||||||
chr5:276973
|
G | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+4201G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 276973 | ||||||
chr5:277096
|
A | C | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+4324A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277096 | ||||||
chr5:277165
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.163+4393G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277165 | ||||||
chr5:277179
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+4407G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277179 | ||||||
chr5:277187
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+4415A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277187 | ||||||
chr5:277190
|
C | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+4418C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277190 | ||||||
chr5:277263
|
C | CT | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+4492dupT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277263 | |||||
chr5:277276
|
C | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.163+4504C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277276 | ||||||
chr5:277299
|
GTA | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(8): Show | 13 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+4529_163+4530d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277299 | |||||
chr5:277301
|
A | AT | 8 | a0001c0001t0003g0064a0001c0002t0001g0002a0001c0002t0001g0050others(5): Show | 10 | HG00438.hp1 HG01952.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+4551dupT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277301 | |||||
chr5:277301
|
A | T | 5 | a0001c0002t0001g0052a0001c0002t0001g0095a0001c0002t0001g0132others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+4529A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277301 | ||||||
chr5:277301
|
AT | A | 65 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(62): Show | 65 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.163+4551delT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277301 | |||||
chr5:277301
|
ATT | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.163+4550_163+4551d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277301 | |||||
chr5:277307
|
T | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00741.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.163+4535T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277307 | ||||||
chr5:277340
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.163+4568C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277340 | ||||||
chr5:277341
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+4569G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277341 | ||||||
chr5:277363
|
A | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.163+4591A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277363 | ||||||
chr5:277379
|
G | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0087 | 4 | NA18980.hp2 NA19012.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+4607G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277379 | ||||||
chr5:277415
|
C | T | 1 | a0001c0002t0001g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.163+4643C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277415 | ||||||
chr5:277502
|
C | T | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+4730C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277502 | ||||||
chr5:277545
|
C | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+4773C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277545 | ||||||
chr5:277710
|
G | A | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+4938G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277710 | ||||||
chr5:277870
|
G | A | 1 | a0001c0002t0001g0335 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163+5098G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277870 | ||||||
chr5:277912
|
C | CA | 109 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 116 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.163+5158dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277912 | |||||
chr5:277912
|
C | CAA | 12 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(9): Show | 13 | HG00280.hp1 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.163+5157_163+5158d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277912 | |||||
chr5:277912
|
C | CAAA | 22 | a0001c0001t0001g0264a0001c0001t0002g0008a0001c0001t0002g0065others(19): Show | 23 | HG01261.hp2 HG02145.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.163+5156_163+5158d others(5): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277912 | |||||
chr5:277912
|
CA | C | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(6): Show | 9 | HG00738.hp1 HG01070.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+5158delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 277912 | |||||
chr5:277943
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+5171C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 277943 | ||||||
chr5:278025
|
C | T | 1 | a0001c0001t0006g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.163+5253C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278025 | ||||||
chr5:278184
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+5412G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278184 | ||||||
chr5:278347
|
T | C | 1 | a0002c0003t0001g0295 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163+5575T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278347 | ||||||
chr5:278377
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.163+5605G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278377 | ||||||
chr5:278389
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+5617T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278389 | ||||||
chr5:278526
|
A | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+5754A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278526 | ||||||
chr5:278546
|
C | CA | 10 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(7): Show | 10 | HG02004.hp1 HG02132.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+5790dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 278546 | |||||
chr5:278546
|
CA | C | 44 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(41): Show | 49 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.163+5790delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 278546 | |||||
chr5:278609
|
A | G | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+5837A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278609 | ||||||
chr5:278637
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+5865T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278637 | ||||||
chr5:278731
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+5959G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278731 | ||||||
chr5:278790
|
GGGAGGGT others(33): Show |
G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+6037_163+6076d others(42): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 278790 | |||||
chr5:278956
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+6184T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 278956 | ||||||
chr5:279036
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163+6264C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279036 | ||||||
chr5:279112
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.163+6340C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279112 | ||||||
chr5:279142
|
C | G | 1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.163+6370C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279142 | ||||||
chr5:279204
|
C | G | 1 | a0001c0002t0001g0130 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.163+6432C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279204 | ||||||
chr5:279205
|
C | CG | 66 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(63): Show | 68 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.163+6433_163+6434i others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279205 | ||||||
chr5:279217
|
C | G | 3 | a0001c0002t0001g0098a0001c0002t0001g0128a0001c0002t0001g0129 | 3 | NA18973.hp1 NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.163+6445C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279217 | ||||||
chr5:279218
|
G | A | 323 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(320): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.163+6446G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279218 | ||||||
chr5:279254
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163+6482A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279254 | ||||||
chr5:279274
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+6502T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279274 | ||||||
chr5:279319
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+6547G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279319 | ||||||
chr5:279397
|
G | A | 43 | a0001c0001t0003g0310a0002c0003t0001g0274a0002c0003t0001g0277others(40): Show | 44 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.163+6625G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279397 | ||||||
chr5:279438
|
G | T | 1 | a0001c0001t0002g0073 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.163+6666G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279438 | ||||||
chr5:279522
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.163+6750G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279522 | ||||||
chr5:279571
|
C | T | 72 | a0001c0001t0001g0246a0001c0001t0002g0008a0001c0001t0002g0065others(69): Show | 75 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.163+6799C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279571 | ||||||
chr5:279598
|
G | C | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+6826G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279598 | ||||||
chr5:279610
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+6838C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279610 | ||||||
chr5:279643
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+6871A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279643 | ||||||
chr5:279662
|
T | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+6890T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279662 | ||||||
chr5:279684
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.163+6912A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279684 | ||||||
chr5:279783
|
C | CA | 36 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(33): Show | 37 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.163+7034dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 279783 | |||||
chr5:279783
|
CA | C | 16 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0190others(13): Show | 16 | HG00609.hp2 HG02027.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+7034delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 279783 | |||||
chr5:279783
|
CAA | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 89 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.163+7033_163+7034d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 279783 | |||||
chr5:279783
|
CAAA | C | 38 | a0002c0003t0001g0274a0002c0003t0001g0283a0002c0003t0001g0284others(35): Show | 39 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.163+7032_163+7034d others(5): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 279783 | |||||
chr5:279794
|
A | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0262a0001c0002t0001g0118 | 3 | HG00738.hp2 HG01358.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.163+7022A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279794 | ||||||
chr5:279803
|
AAAAC | A | 27 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(24): Show | 29 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.163+7032_163+7035d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279803 | ||||||
chr5:279850
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+7078T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279850 | ||||||
chr5:279946
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.163+7174G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279946 | ||||||
chr5:279996
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+7224G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279996 | ||||||
chr5:279999
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+7227G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 279999 | ||||||
chr5:280014
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.163+7242G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280014 | ||||||
chr5:280072
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.163+7300A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280072 | ||||||
chr5:280129
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+7357A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280129 | ||||||
chr5:280199
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+7427C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280199 | ||||||
chr5:280200
|
C | G | 4 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 5 | HG02145.hp2 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+7428C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280200 | ||||||
chr5:280294
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.163+7522C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280294 | ||||||
chr5:280313
|
CA | C | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+7542delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280313 | ||||||
chr5:280549
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+7777G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280549 | ||||||
chr5:280955
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+8183G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280955 | ||||||
chr5:280982
|
A | C | 1 | a0002c0004t0002g0269 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+8210A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 280982 | ||||||
chr5:281098
|
C | T | 31 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(28): Show | 31 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.163+8326C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281098 | ||||||
chr5:281166
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.163+8394G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281166 | ||||||
chr5:281202
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.163+8430T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281202 | ||||||
chr5:281399
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.163+8627G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281399 | ||||||
chr5:281470
|
A | G | 1 | a0002c0003t0001g0294 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.163+8698A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281470 | ||||||
chr5:281491
|
G | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+8719G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281491 | ||||||
chr5:281500
|
G | A | 15 | a0002c0003t0001g0277a0002c0003t0001g0278a0002c0003t0001g0283others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+8728G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281500 | ||||||
chr5:281584
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.163+8812A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281584 | ||||||
chr5:281785
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.163+9013G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281785 | ||||||
chr5:281795
|
A | G | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+9023A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281795 | ||||||
chr5:281869
|
G | C | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9097G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 281869 | ||||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0002c0003t0001g0286 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0002c0004t0003g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2593): Show |
1 | a0002c0003t0001g0301 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.163+9162_163+9163i others(2602): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0002c0003t0007g0287 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
22 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(19): Show | 22 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2596): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.163+9162_163+9163i others(2605): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0001c0001t0002g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0002c0004t0003g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
19 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(16): Show | 20 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
4 | a0001c0001t0002g0081a0002c0004t0003g0281a0002c0004t0003g0282others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2547): Show |
2 | a0001c0001t0005g0272a0001c0001t0005g0273 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.163+9163_163+9164i others(2556): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2547): Show |
3 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271 | 4 | HG02647.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+9163_163+9164i others(2556): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2594): Show |
1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+9163_163+9164i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281895
|
T | TCGGGGAG others(2690): Show |
1 | a0001c0001t0002g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163+9163_163+9164i others(2699): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281895 | |||||
chr5:281931
|
C | CAGCCGAA others(2594): Show |
5 | a0002c0004t0002g0269a0002c0004t0003g0265a0002c0004t0003g0266others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+9162_163+9163i others(2603): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 281931 | |||||
chr5:282272
|
C | CG | 18 | a0001c0001t0001g0176a0001c0001t0001g0241a0001c0001t0001g0251others(15): Show | 18 | HG00609.hp2 HG02165.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.163+9511dupG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 282272 | |||||
chr5:282272
|
CG | C | 68 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(65): Show | 70 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.163+9511delG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 282272 | |||||
chr5:282272
|
CGG | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(15): Show | 20 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.163+9510_163+9511d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 282272 | |||||
chr5:282275
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+9503G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282275 | ||||||
chr5:282275
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.163+9503G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282275 | ||||||
chr5:282276
|
G | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.163+9504G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282276 | ||||||
chr5:282276
|
G | T | 1 | a0001c0002t0001g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163+9504G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282276 | ||||||
chr5:282279
|
G | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+9507G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282279 | ||||||
chr5:282305
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.163+9533G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282305 | ||||||
chr5:282320
|
A | C | 1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.163+9548A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282320 | ||||||
chr5:282420
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.163+9648C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282420 | ||||||
chr5:282683
|
C | G | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+9911C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282683 | ||||||
chr5:282761
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163+9989G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282761 | ||||||
chr5:282761
|
G | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.163+9989G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 282761 | ||||||
chr5:283165
|
C | A | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+10393C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283165 | ||||||
chr5:283362
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0186a0001c0001t0001g0187others(5): Show | 9 | HG00673.hp1 HG01167.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.163+10590G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283362 | ||||||
chr5:283404
|
G | A | 26 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(23): Show | 27 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.163+10632G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283404 | ||||||
chr5:283452
|
A | ACCCCCCC others(19): Show |
1 | a0002c0003t0001g0301 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.163+10683_163+1068 others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 283452 | |||||
chr5:283502
|
C | T | 1 | a0002c0004t0003g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+10730C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283502 | ||||||
chr5:283582
|
T | A | 1 | a0001c0001t0002g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.163+10810T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283582 | ||||||
chr5:283765
|
T | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+10993T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283765 | ||||||
chr5:283802
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.163+11030C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283802 | ||||||
chr5:283932
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.163+11160G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 283932 | ||||||
chr5:284002
|
G | T | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+11230G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284002 | ||||||
chr5:284007
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+11235G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284007 | ||||||
chr5:284073
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.163+11301G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284073 | ||||||
chr5:284136
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+11364A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284136 | ||||||
chr5:284266
|
G | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+11494G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284266 | ||||||
chr5:284302
|
G | GAGGAGGA others(84): Show |
4 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02602.hp1 HG03239.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+11548_163+1163 others(95): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 284302 | |||||
chr5:284378
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163+11606C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284378 | ||||||
chr5:284410
|
C | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+11638C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284410 | ||||||
chr5:284413
|
A | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.163+11641A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284413 | ||||||
chr5:284439
|
T | C | 336 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(333): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.163+11667T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284439 | ||||||
chr5:284518
|
G | A | 1 | a0001c0002t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.163+11746G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284518 | ||||||
chr5:284519
|
G | A | 1 | a0002c0004t0003g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+11747G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284519 | ||||||
chr5:284639
|
C | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+11867C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284639 | ||||||
chr5:284641
|
GTGCAGCT others(39): Show |
G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+11884_163+1192 others(50): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 284641 | |||||
chr5:284687
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(156): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.163+11915A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284687 | ||||||
chr5:284781
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.163+12009G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284781 | ||||||
chr5:284825
|
G | A | 2 | a0001c0001t0001g0191a0001c0002t0001g0120 | 2 | HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.163+12053G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284825 | ||||||
chr5:284827
|
G | C | 1 | a0001c0002t0001g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.163+12055G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284827 | ||||||
chr5:284874
|
C | CG | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+12105dupG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 284874 | |||||
chr5:284890
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.163+12118C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 284890 | ||||||
chr5:285048
|
C | T | 1 | a0001c0001t0005g0272 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163+12276C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285048 | ||||||
chr5:285171
|
C | T | 1 | a0002c0004t0003g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163+12399C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285171 | ||||||
chr5:285218
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.163+12446C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285218 | ||||||
chr5:285281
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+12509C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285281 | ||||||
chr5:285328
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.163+12556C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285328 | ||||||
chr5:285330
|
G | A | 1 | a0001c0002t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.163+12558G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285330 | ||||||
chr5:285364
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+12592G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285364 | ||||||
chr5:285469
|
G | A | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+12697G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285469 | ||||||
chr5:285552
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+12780A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285552 | ||||||
chr5:285633
|
C | G | 74 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(71): Show | 77 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.163+12861C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285633 | ||||||
chr5:285912
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+13140A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285912 | ||||||
chr5:285962
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.163+13190T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285962 | ||||||
chr5:285964
|
C | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0186a0001c0001t0001g0187others(5): Show | 9 | HG00673.hp1 HG01167.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.163+13192C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285964 | ||||||
chr5:285977
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163+13205C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285977 | ||||||
chr5:285978
|
G | A | 1 | a0002c0004t0003g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+13206G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285978 | ||||||
chr5:285994
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+13222A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 285994 | ||||||
chr5:286048
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+13276G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286048 | ||||||
chr5:286094
|
A | AG | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+13328dupG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 286094 | |||||
chr5:286096
|
G | C | 1 | a0001c0002t0001g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163+13324G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286096 | ||||||
chr5:286159
|
G | A | 1 | a0001c0002t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.163+13387G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286159 | ||||||
chr5:286236
|
C | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+13464C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286236 | ||||||
chr5:286288
|
G | A | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG01943.hp1 NA18939.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+13516G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286288 | ||||||
chr5:286331
|
G | A | 1 | a0002c0003t0001g0293 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163+13559G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286331 | ||||||
chr5:286355
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18987.hp1 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.163+13583C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286355 | ||||||
chr5:286367
|
G | A | 3 | a0001c0002t0001g0136a0001c0002t0001g0317a0001c0002t0001g0318 | 3 | NA18980.hp1 NA19002.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.163+13595G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286367 | ||||||
chr5:286372
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+13600G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286372 | ||||||
chr5:286391
|
C | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.163+13619C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286391 | ||||||
chr5:286408
|
G | A | 1 | a0001c0002t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.163+13636G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286408 | ||||||
chr5:286409
|
C | A | 1 | a0001c0002t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.163+13637C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286409 | ||||||
chr5:286504
|
C | T | 1 | a0002c0003t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.163+13732C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286504 | ||||||
chr5:286613
|
G | A | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.163+13841G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286613 | ||||||
chr5:286654
|
G | C | 1 | a0001c0001t0001g0014 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.163+13882G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286654 | ||||||
chr5:286674
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163+13902G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286674 | ||||||
chr5:286691
|
CTGGAGAC others(40): Show |
C | 1 | a0002c0003t0001g0303 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.163+13946_163+1399 others(51): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 286691 | |||||
chr5:286720
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.163+13948C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286720 | ||||||
chr5:286837
|
G | A | 1 | a0001c0002t0001g0320 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.163+14065G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286837 | ||||||
chr5:286884
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.163+14112G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286884 | ||||||
chr5:286904
|
C | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+14132C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 286904 | ||||||
chr5:287082
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.163+14310C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287082 | ||||||
chr5:287171
|
C | T | 5 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0113others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+14399C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287171 | ||||||
chr5:287293
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+14521G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287293 | ||||||
chr5:287306
|
C | T | 1 | a0002c0003t0001g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+14534C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287306 | ||||||
chr5:287307
|
G | A | 27 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(24): Show | 28 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.163+14535G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287307 | ||||||
chr5:287363
|
A | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.163+14591A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287363 | ||||||
chr5:287366
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18987.hp1 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.163+14594T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287366 | ||||||
chr5:287420
|
ATGCATTC others(19): Show |
A | 3 | a0002c0004t0003g0281a0002c0004t0003g0282a0002c0004t0003g0298 | 3 | HG00735.hp1 HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.163+14651_163+1467 others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 287420 | |||||
chr5:287453
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163+14681T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287453 | ||||||
chr5:287634
|
A | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+14862A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287634 | ||||||
chr5:287731
|
G | A | 1 | a0002c0004t0003g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.163+14959G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287731 | ||||||
chr5:287792
|
A | G | 38 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(35): Show | 39 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.163+15020A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287792 | ||||||
chr5:287861
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.163+15089C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287861 | ||||||
chr5:287873
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0048 | 2 | NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.163+15101G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287873 | ||||||
chr5:287899
|
T | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.163+15127T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 287899 | ||||||
chr5:288232
|
T | C | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+15460T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288232 | ||||||
chr5:288292
|
T | TAATA | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+15520_163+1552 others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288292 | ||||||
chr5:288292
|
T | TAATATA | 18 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(15): Show | 19 | HG02145.hp2 HG02273.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.163+15520_163+1552 others(10): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288292 | ||||||
chr5:288292
|
T | TAATATAT others(1): Show |
5 | a0001c0001t0002g0065a0001c0001t0002g0078a0001c0001t0002g0079others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+15520_163+1552 others(12): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288292 | ||||||
chr5:288292
|
T | TAATATAT others(3): Show |
3 | a0002c0004t0003g0281a0002c0004t0003g0282a0002c0004t0003g0298 | 3 | HG00735.hp1 HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.163+15520_163+1552 others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288292 | ||||||
chr5:288292
|
T | TAATATAT others(7): Show |
1 | a0002c0004t0003g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.163+15520_163+1552 others(18): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288292 | ||||||
chr5:288292
|
T | TTA | 10 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0164others(7): Show | 10 | HG00280.hp1 HG00544.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+15539_163+1554 others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288292 | |||||
chr5:288292
|
T | TTTTATA | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | NA18939.hp2 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+15521_163+1552 others(10): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288292 | |||||
chr5:288293
|
T | A | 45 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(42): Show | 47 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.163+15521T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288293 | ||||||
chr5:288294
|
A | T | 3 | a0001c0002t0001g0104a0001c0002t0001g0106a0002c0004t0003g0279 | 3 | HG02572.hp2 NA18948.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.163+15522A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288294 | ||||||
chr5:288306
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.163+15534A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288306 | ||||||
chr5:288307
|
T | C | 1 | a0002c0004t0003g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+15535T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288307 | ||||||
chr5:288309
|
T | C | 32 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(29): Show | 32 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.163+15537T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288309 | ||||||
chr5:288311
|
T | C | 34 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(31): Show | 35 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.163+15539T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288311 | ||||||
chr5:288311
|
T | TATAC | 77 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 80 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.163+15540_163+1554 others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288311 | |||||
chr5:288311
|
T | TATATAC | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0220others(7): Show | 10 | HG00621.hp1 HG01943.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+15540_163+1554 others(10): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288311 | |||||
chr5:288311
|
TAC | T | 32 | a0001c0001t0003g0310a0002c0003t0001g0274a0002c0003t0001g0277others(29): Show | 32 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.163+15543_163+1554 others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288311 | |||||
chr5:288313
|
C | T | 11 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(8): Show | 13 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+15541C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288313 | ||||||
chr5:288352
|
C | G | 6 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(3): Show | 10 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+15580C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288352 | ||||||
chr5:288495
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.164-15682T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288495 | ||||||
chr5:288534
|
C | T | 1 | a0002c0003t0001g0291 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.164-15643C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288534 | ||||||
chr5:288604
|
AAAAG | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-15555_164-1555 others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288604 | |||||
chr5:288715
|
ATTG | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-15459_164-1545 others(7): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 288715 | |||||
chr5:288718
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-15459G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288718 | ||||||
chr5:288811
|
T | C | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-15366T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288811 | ||||||
chr5:288923
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.164-15254A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 288923 | ||||||
chr5:289038
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.164-15139G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289038 | ||||||
chr5:289102
|
A | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-15075A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289102 | ||||||
chr5:289291
|
A | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-14886A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289291 | ||||||
chr5:289441
|
C | T | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.164-14736C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289441 | ||||||
chr5:289527
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.164-14650G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289527 | ||||||
chr5:289562
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-14615C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289562 | ||||||
chr5:289585
|
C | G | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-14592C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289585 | ||||||
chr5:289643
|
A | G | 3 | a0002c0004t0003g0281a0002c0004t0003g0282a0002c0004t0003g0298 | 3 | HG00735.hp1 HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.164-14534A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289643 | ||||||
chr5:289759
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.164-14418G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289759 | ||||||
chr5:289789
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0163 | 2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.164-14388C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289789 | ||||||
chr5:289963
|
A | C | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-14214A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 289963 | ||||||
chr5:290083
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-14094T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290083 | ||||||
chr5:290183
|
A | G | 1 | a0002c0003t0001g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-13994A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290183 | ||||||
chr5:290216
|
C | G | 1 | a0001c0002t0001g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.164-13961C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290216 | ||||||
chr5:290282
|
C | A | 1 | a0001c0002t0001g0127 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.164-13895C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290282 | ||||||
chr5:290307
|
A | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-13870A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290307 | ||||||
chr5:290391
|
C | T | 1 | a0002c0003t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.164-13786C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290391 | ||||||
chr5:290445
|
T | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-13732T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290445 | ||||||
chr5:290640
|
T | TA | 12 | a0001c0002t0001g0003a0001c0002t0001g0151a0001c0002t0001g0172others(9): Show | 14 | HG02273.hp1 HG03710.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-13536dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 290640 | |||||
chr5:290705
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0163 | 2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.164-13472G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290705 | ||||||
chr5:290901
|
C | T | 2 | a0001c0001t0003g0310a0001c0002t0001g0094 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.164-13276C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290901 | ||||||
chr5:290941
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164-13236A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 290941 | ||||||
chr5:290941
|
AAGT | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-13234_164-1323 others(7): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 290941 | |||||
chr5:291086
|
A | C | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-13091A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291086 | ||||||
chr5:291208
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-12969T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291208 | ||||||
chr5:291261
|
G | A | 1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-12916G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291261 | ||||||
chr5:291361
|
CCTCCATT others(328): Show |
C | 11 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0001g0201others(8): Show | 11 | HG00597.hp2 HG02135.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-12750_164-1241 others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 291361 | |||||
chr5:291426
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-12751C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291426 | ||||||
chr5:291483
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.164-12694C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291483 | ||||||
chr5:291530
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.164-12647A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291530 | ||||||
chr5:291546
|
G | GCTGCGTG others(60): Show |
46 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.164-12580_164-1251 others(71): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 291546 | |||||
chr5:291592
|
C | G | 1 | a0001c0002t0001g0318 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.164-12585C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291592 | ||||||
chr5:291613
|
ACTGCGTG others(60): Show |
A | 1 | a0001c0002t0001g0060 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-12509_164-1244 others(71): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 291613 | |||||
chr5:291616
|
G | C | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.164-12561G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291616 | ||||||
chr5:291618
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02886.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-12559G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291618 | ||||||
chr5:291628
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0048 | 2 | NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.164-12549G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291628 | ||||||
chr5:291664
|
A | G | 6 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(3): Show | 7 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-12513A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291664 | ||||||
chr5:291694
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-12483C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291694 | ||||||
chr5:291695
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-12482G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291695 | ||||||
chr5:291820
|
A | G | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-12357A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291820 | ||||||
chr5:291856
|
G | A | 1 | a0002c0004t0003g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.164-12321G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291856 | ||||||
chr5:291987
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.164-12190A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 291987 | ||||||
chr5:292033
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.164-12144C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292033 | ||||||
chr5:292145
|
C | G | 2 | a0001c0001t0001g0164a0001c0002t0001g0138 | 2 | HG02683.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.164-12032C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292145 | ||||||
chr5:292196
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-11981A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292196 | ||||||
chr5:292202
|
G | T | 1 | a0001c0002t0001g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.164-11975G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292202 | ||||||
chr5:292249
|
C | A | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-11928C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292249 | ||||||
chr5:292307
|
GGAATGCA others(7): Show |
G | 5 | a0001c0002t0001g0052a0001c0002t0001g0095a0001c0002t0001g0132others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-11867_164-1185 others(18): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 292307 | |||||
chr5:292404
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-11773G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292404 | ||||||
chr5:292562
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0115 | 2 | HG01496.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.164-11615C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292562 | ||||||
chr5:292581
|
A | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-11596A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292581 | ||||||
chr5:292826
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-11351C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292826 | ||||||
chr5:292862
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(2): Show | 7 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-11315C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292862 | ||||||
chr5:292915
|
G | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-11262G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 292915 | ||||||
chr5:293202
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.164-10975A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293202 | ||||||
chr5:293229
|
TGATCAAG others(713): Show |
T | 1 | a0001c0001t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.164-10924_164-1020 others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293229 | |||||
chr5:293278
|
A | ACGATACT others(173): Show |
1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.164-10869_164-1086 others(184): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293278 | |||||
chr5:293284
|
C | CTGTCAGA others(84): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-10835_164-1083 others(95): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293284 | |||||
chr5:293284
|
CTGTCAGA others(83): Show |
C | 1 | a0001c0001t0001g0235 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.164-10810_164-1072 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293284 | |||||
chr5:293301
|
A | G | 1 | a0001c0002t0001g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.164-10876A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293301 | ||||||
chr5:293367
|
T | C | 189 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.164-10810T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293367 | ||||||
chr5:293368
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0080 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.164-10809G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293368 | ||||||
chr5:293374
|
A | ATGTCAGA others(353): Show |
1 | a0001c0001t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.164-10794_164-1079 others(364): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293374 | |||||
chr5:293374
|
A | ATGTCAGA others(623): Show |
1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.164-10794_164-1079 others(634): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293374 | |||||
chr5:293374
|
A | C | 32 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(29): Show | 34 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.164-10803A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293374 | ||||||
chr5:293384
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0143others(12): Show | 17 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-10793T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293384 | ||||||
chr5:293384
|
T | TGGAGAAA others(83): Show |
1 | a0001c0002t0001g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.164-10704_164-1070 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293384 | |||||
chr5:293384
|
TGGAGAAA others(263): Show |
T | 2 | a0001c0002t0001g0028a0001c0002t0001g0046 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.164-10703_164-1043 others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293384 | |||||
chr5:293393
|
G | GTATGACA others(173): Show |
2 | a0001c0001t0002g0008a0001c0001t0002g0066 | 3 | HG03041.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.164-10614_164-1061 others(184): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293393 | |||||
chr5:293432
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.164-10745C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293432 | ||||||
chr5:293464
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.164-10713C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293464 | ||||||
chr5:293474
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.164-10703T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293474 | ||||||
chr5:293474
|
T | TGGAGAAA others(83): Show |
4 | a0001c0002t0001g0005a0001c0002t0001g0038a0001c0002t0001g0130others(1): Show | 5 | HG02300.hp1 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-10239_164-1015 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293474 | |||||
chr5:293474
|
T | TGGAGAAA others(893): Show |
1 | a0001c0001t0001g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.164-10354_164-1035 others(904): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293474 | |||||
chr5:293474
|
TGGAGAAA others(83): Show |
T | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.164-10239_164-1015 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293474 | |||||
chr5:293474
|
TGGAGAAA others(173): Show |
T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG00621.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-10329_164-1015 others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293474 | |||||
chr5:293474
|
TGGAGAAA others(263): Show |
T | 2 | a0001c0002t0001g0026a0001c0002t0001g0137 | 2 | HG03017.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.164-10419_164-1015 others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293474 | |||||
chr5:293476
|
G | A | 1 | a0001c0002t0001g0311 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.164-10701G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293476 | ||||||
chr5:293522
|
C | CGAGGCAC others(533): Show |
1 | a0001c0001t0001g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.164-10150_164-1014 others(544): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293522 | |||||
chr5:293548
|
G | A | 1 | a0001c0002t0001g0313 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.164-10629G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293548 | ||||||
chr5:293564
|
C | T | 72 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(69): Show | 75 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.164-10613C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293564 | ||||||
chr5:293565
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.164-10612G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293565 | ||||||
chr5:293573
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0084 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.164-10604G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293573 | ||||||
chr5:293640
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0066 | 3 | HG03041.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.164-10537G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293640 | ||||||
chr5:293654
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10523C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293654 | ||||||
chr5:293744
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10433C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293744 | ||||||
chr5:293801
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.164-10376G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293801 | ||||||
chr5:293814
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-10363G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293814 | ||||||
chr5:293820
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0084 | 3 | HG02145.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.164-10357G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293820 | ||||||
chr5:293834
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10343C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293834 | ||||||
chr5:293907
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.164-10270C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293907 | ||||||
chr5:293908
|
G | GCGATACT others(83): Show |
16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-10184_164-1018 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293908 | |||||
chr5:293924
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10253C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293924 | ||||||
chr5:293961
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-10216C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293961 | ||||||
chr5:293972
|
C | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10205C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293972 | ||||||
chr5:293974
|
A | AGGCACTG others(353): Show |
19 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(16): Show | 19 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-10164_164-1016 others(364): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293974 | |||||
chr5:293974
|
A | AGGCACTG others(173): Show |
38 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(35): Show | 39 | HG00642.hp2 HG00735.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.164-10164_164-1016 others(184): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293974 | |||||
chr5:293974
|
A | AGGCACTG others(83): Show |
1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-10164_164-1016 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293974 | |||||
chr5:293974
|
A | AGGCACTG others(173): Show |
4 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 5 | HG02145.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-10164_164-1016 others(184): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293974 | |||||
chr5:293974
|
A | AGGCACTG others(83): Show |
4 | a0002c0003t0001g0291a0002c0003t0001g0304a0002c0003t0007g0287others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-10179_164-1017 others(94): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 293974 | |||||
chr5:293974
|
A | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10203A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 293974 | ||||||
chr5:294014
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10163C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294014 | ||||||
chr5:294083
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.164-10094A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294083 | ||||||
chr5:294088
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10089G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294088 | ||||||
chr5:294126
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10051A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294126 | ||||||
chr5:294157
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10020C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294157 | ||||||
chr5:294162
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-10015C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294162 | ||||||
chr5:294211
|
T | A | 1 | a0001c0002t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.164-9966T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294211 | ||||||
chr5:294218
|
T | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9959T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294218 | ||||||
chr5:294224
|
G | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9953G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294224 | ||||||
chr5:294237
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9940A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294237 | ||||||
chr5:294239
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9938A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294239 | ||||||
chr5:294246
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9931T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294246 | ||||||
chr5:294267
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9910C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294267 | ||||||
chr5:294280
|
T | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9897T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294280 | ||||||
chr5:294283
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9894A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294283 | ||||||
chr5:294284
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9893C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294284 | ||||||
chr5:294367
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9810G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294367 | ||||||
chr5:294396
|
G | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9781G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294396 | ||||||
chr5:294400
|
C | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9777C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294400 | ||||||
chr5:294401
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9776A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294401 | ||||||
chr5:294419
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.164-9758G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294419 | ||||||
chr5:294490
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9687A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294490 | ||||||
chr5:294495
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-9682C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294495 | ||||||
chr5:294585
|
T | A | 1 | a0001c0002t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.164-9592T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294585 | ||||||
chr5:294609
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.164-9568G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294609 | ||||||
chr5:294834
|
A | T | 1 | a0001c0001t0001g0264 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.164-9343A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294834 | ||||||
chr5:294896
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9281C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294896 | ||||||
chr5:294903
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9274A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294903 | ||||||
chr5:294922
|
G | C | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-9255G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294922 | ||||||
chr5:294927
|
G | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-9250G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294927 | ||||||
chr5:294945
|
C | T | 4 | a0001c0002t0001g0095a0001c0002t0001g0132a0001c0002t0001g0133others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-9232C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294945 | ||||||
chr5:294949
|
A | G | 2 | a0001c0001t0001g0092a0001c0002t0001g0025 | 2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.164-9228A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294949 | ||||||
chr5:294951
|
G | A | 2 | a0001c0001t0001g0092a0001c0002t0001g0025 | 2 | HG02132.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.164-9226G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294951 | ||||||
chr5:294954
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-9223A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 294954 | ||||||
chr5:295043
|
T | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-9134T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295043 | ||||||
chr5:295093
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-9084G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295093 | ||||||
chr5:295210
|
AAAAT | A | 40 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(37): Show | 41 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.164-8963_164-8960d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 295210 | |||||
chr5:295214
|
T | A | 1 | a0002c0004t0003g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.164-8963T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295214 | ||||||
chr5:295214
|
T | TA | 29 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(26): Show | 31 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-8956dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 295214 | |||||
chr5:295222
|
C | A | 64 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(61): Show | 66 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.164-8955C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295222 | ||||||
chr5:295227
|
A | C | 1 | a0002c0004t0003g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.164-8950A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295227 | ||||||
chr5:295387
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.164-8790C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295387 | ||||||
chr5:295388
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-8789G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295388 | ||||||
chr5:295438
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-8739C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295438 | ||||||
chr5:295479
|
A | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(185): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.164-8698A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295479 | ||||||
chr5:295489
|
T | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.164-8688T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295489 | ||||||
chr5:295502
|
A | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.164-8675A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295502 | ||||||
chr5:295503
|
G | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.164-8674G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295503 | ||||||
chr5:295518
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.164-8659A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295518 | ||||||
chr5:295607
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(99): Show | 107 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.164-8570C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295607 | ||||||
chr5:295645
|
CT | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(16): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-8524delT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 295645 | |||||
chr5:295672
|
C | T | 2 | a0001c0002t0001g0156a0001c0002t0001g0157 | 2 | NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.164-8505C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295672 | ||||||
chr5:295700
|
G | T | 2 | a0002c0004t0003g0276a0002c0004t0003g0290 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.164-8477G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295700 | ||||||
chr5:295712
|
C | G | 9 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-8465C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295712 | ||||||
chr5:295717
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.164-8460C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295717 | ||||||
chr5:295770
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-8407C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295770 | ||||||
chr5:295784
|
C | G | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-8393C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295784 | ||||||
chr5:295830
|
A | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.164-8347A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295830 | ||||||
chr5:295935
|
G | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.164-8242G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 295935 | ||||||
chr5:296058
|
C | T | 3 | a0002c0004t0003g0281a0002c0004t0003g0282a0002c0004t0003g0298 | 3 | HG00735.hp1 HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.164-8119C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296058 | ||||||
chr5:296104
|
A | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-8073A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296104 | ||||||
chr5:296193
|
C | A | 4 | a0002c0004t0003g0280a0002c0004t0003g0281a0002c0004t0003g0282others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-7984C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296193 | ||||||
chr5:296221
|
C | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.164-7956C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296221 | ||||||
chr5:296383
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.164-7794A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296383 | ||||||
chr5:296384
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.164-7793C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296384 | ||||||
chr5:296437
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-7740C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296437 | ||||||
chr5:296569
|
AGT | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-7602_164-7601d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 296569 | |||||
chr5:296626
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.164-7551G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296626 | ||||||
chr5:296626
|
G | T | 1 | a0001c0002t0001g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.164-7551G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296626 | ||||||
chr5:296707
|
T | C | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.164-7470T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296707 | ||||||
chr5:296739
|
G | A | 6 | a0002c0003t0001g0277a0002c0003t0001g0283a0002c0003t0001g0294others(3): Show | 6 | HG00642.hp2 HG01070.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-7438G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296739 | ||||||
chr5:296770
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.164-7407A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296770 | ||||||
chr5:296866
|
AG | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-7308delG | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 296866 | |||||
chr5:296877
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-7300G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296877 | ||||||
chr5:296882
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-7295G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296882 | ||||||
chr5:296946
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.164-7231C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296946 | ||||||
chr5:296951
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.164-7226C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296951 | ||||||
chr5:296976
|
A | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-7201A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 296976 | ||||||
chr5:297024
|
C | T | 23 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-7153C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297024 | ||||||
chr5:297032
|
G | T | 3 | a0001c0002t0001g0332a0001c0002t0001g0333a0001c0002t0001g0334 | 3 | HG00609.hp2 HG02165.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.164-7145G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297032 | ||||||
chr5:297073
|
C | T | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.164-7104C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297073 | ||||||
chr5:297078
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.164-7099C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297078 | ||||||
chr5:297116
|
A | G | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.164-7061A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297116 | ||||||
chr5:297149
|
C | T | 42 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(39): Show | 43 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.164-7028C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297149 | ||||||
chr5:297299
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-6878G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297299 | ||||||
chr5:297304
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.164-6873C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297304 | ||||||
chr5:297342
|
T | A | 1 | a0001c0002t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.164-6835T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297342 | ||||||
chr5:297359
|
C | T | 1 | a0002c0003t0001g0295 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.164-6818C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297359 | ||||||
chr5:297419
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.164-6758G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297419 | ||||||
chr5:297615
|
G | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0106 | 2 | NA18948.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.164-6562G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297615 | ||||||
chr5:297641
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-6536C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297641 | ||||||
chr5:297680
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-6497A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297680 | ||||||
chr5:297909
|
T | C | 1 | a0001c0001t0006g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.164-6268T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 297909 | ||||||
chr5:298007
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.164-6170G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298007 | ||||||
chr5:298118
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.164-6059C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298118 | ||||||
chr5:298151
|
A | T | 1 | a0001c0001t0001g0014 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.164-6026A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298151 | ||||||
chr5:298168
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-6009G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298168 | ||||||
chr5:298192
|
A | G | 2 | a0001c0002t0001g0058a0001c0002t0001g0059 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.164-5985A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298192 | ||||||
chr5:298237
|
C | T | 5 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0307others(2): Show | 6 | HG01891.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5940C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298237 | ||||||
chr5:298321
|
C | T | 1 | a0001c0002t0001g0334 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-5856C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298321 | ||||||
chr5:298330
|
G | A | 1 | a0001c0001t0005g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.164-5847G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298330 | ||||||
chr5:298577
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.164-5600G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298577 | ||||||
chr5:298584
|
A | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.164-5593A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298584 | ||||||
chr5:298644
|
C | CAGCTGCT others(6): Show |
1 | a0001c0001t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.164-5533_164-5532i others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298644 | ||||||
chr5:298644
|
CCAGCTGC others(7): Show |
C | 7 | a0001c0002t0001g0006a0001c0002t0001g0030a0001c0002t0001g0050others(4): Show | 8 | HG01346.hp1 NA18943.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-5477_164-5464d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298644 | |||||
chr5:298658
|
T | TCAGCTGC others(171): Show |
1 | a0001c0002t0001g0318 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.164-5518_164-5341d others(180): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298658 | |||||
chr5:298658
|
T | TCAGCTGC others(35): Show |
91 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-5480_164-5479i others(44): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298658 | |||||
chr5:298658
|
T | TCAGCTGC others(49): Show |
6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | NA18939.hp2 NA18973.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-5480_164-5479i others(58): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298658 | |||||
chr5:298672
|
T | TCAGCTGC others(21): Show |
13 | a0001c0001t0001g0167a0001c0001t0001g0195a0001c0001t0001g0206others(10): Show | 13 | HG00673.hp1 HG00741.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-5480_164-5479i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298672 | |||||
chr5:298672
|
T | TCAGCTGC others(35): Show |
1 | a0001c0001t0001g0217 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.164-5480_164-5479i others(44): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298672 | |||||
chr5:298672
|
T | TCAGCTGC others(7): Show |
5 | a0001c0001t0003g0310a0002c0004t0003g0265a0002c0004t0003g0266others(2): Show | 5 | HG02451.hp2 HG02486.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-5494_164-5493i others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298672 | |||||
chr5:298683
|
CA | C | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.164-5493delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298683 | ||||||
chr5:298684
|
A | C | 46 | a0001c0001t0001g0143a0001c0001t0001g0169a0001c0001t0001g0170others(43): Show | 48 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.164-5493A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298684 | ||||||
chr5:298686
|
T | C | 70 | a0001c0001t0001g0143a0001c0001t0001g0169a0001c0001t0001g0170others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-5491T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298686 | ||||||
chr5:298686
|
T | TCAGCTGC others(21): Show |
1 | a0001c0002t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.164-5477_164-5450d others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298686 | |||||
chr5:298686
|
T | TCAGCTGC others(7): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0149 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-5480_164-5479i others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298686 | |||||
chr5:298686
|
T | TCAGCTGC others(35): Show |
1 | a0002c0004t0003g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-5480_164-5479i others(44): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298686 | |||||
chr5:298700
|
T | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.164-5477T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298700 | ||||||
chr5:298712
|
A | C | 1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.164-5465A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298712 | ||||||
chr5:298714
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG02886.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5463C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298714 | ||||||
chr5:298725
|
CA | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.164-5451delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298725 | ||||||
chr5:298726
|
A | ACCCAGCT others(20): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-5439_164-5438i others(29): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298726 | |||||
chr5:298726
|
A | ACCCAGCT others(6): Show |
4 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00673.hp1 HG01943.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-5439_164-5427d others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298726 | |||||
chr5:298726
|
A | ACCCAGCT others(34): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-5438_164-5437i others(43): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298726 | |||||
chr5:298726
|
A | ACCCAGCT others(21): Show |
35 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(32): Show | 36 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.164-5438_164-5437i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298726 | |||||
chr5:298726
|
A | ACTCAGCT others(48): Show |
1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.164-5450_164-5449i others(57): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298726 | |||||
chr5:298726
|
A | C | 5 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(2): Show | 5 | HG02451.hp2 HG02486.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-5451A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298726 | ||||||
chr5:298728
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.164-5449C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298728 | ||||||
chr5:298739
|
C | CA | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-5438_164-5437i others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298739 | ||||||
chr5:298750
|
CA | C | 24 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(21): Show | 25 | HG00741.hp1 HG02257.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.164-5426delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298750 | ||||||
chr5:298751
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.164-5426A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298751 | ||||||
chr5:298752
|
C | CCCCAGCT others(5): Show |
1 | a0001c0001t0001g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.164-5422_164-5421i others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298752 | |||||
chr5:298758
|
A | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 106 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.164-5419A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298758 | ||||||
chr5:298765
|
C | A | 14 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(11): Show | 15 | HG02257.hp1 HG02280.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.164-5412C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298765 | ||||||
chr5:298779
|
C | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-5398C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298779 | ||||||
chr5:298784
|
C | CAGCTGCT others(26): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-5381_164-5380i others(35): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298784 | |||||
chr5:298786
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-5391G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298786 | ||||||
chr5:298791
|
T | TC | 33 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(30): Show | 35 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.164-5381dupC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298791 | |||||
chr5:298791
|
T | TCC | 49 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(46): Show | 50 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.164-5382_164-5381d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298791 | |||||
chr5:298791
|
T | TCCCCCAG others(6): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-5380_164-5368d others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298791 | |||||
chr5:298808
|
CCT | C | 9 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(6): Show | 9 | HG02602.hp1 HG03239.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-5368_164-5367d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298808 | ||||||
chr5:298810
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(1): Show | 4 | HG02922.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-5367T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298810 | ||||||
chr5:298819
|
C | A | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.164-5358C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298819 | ||||||
chr5:298822
|
C | CCAGCTGC others(33): Show |
1 | a0001c0001t0002g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-5354_164-5353i others(42): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CCAGCTGC others(47): Show |
22 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(19): Show | 23 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-5354_164-5353i others(56): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CCAGCTGC others(47): Show |
1 | a0001c0001t0002g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.164-5354_164-5353i others(56): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CCAGCTGC others(34): Show |
30 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(27): Show | 30 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.164-5354_164-5353i others(43): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CCAGCTGC others(34): Show |
6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-5354_164-5353i others(43): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CCAGCTGC others(20): Show |
4 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(1): Show | 4 | HG02451.hp2 HG02486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-5354_164-5353i others(29): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298822 | |||||
chr5:298822
|
C | CGAGCTGC others(47): Show |
5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5355_164-5354i others(56): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298822 | ||||||
chr5:298822
|
C | G | 1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-5355C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298822 | ||||||
chr5:298823
|
CCAGCTGC others(7): Show |
C | 1 | a0001c0002t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.164-5340_164-5327d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298823 | |||||
chr5:298824
|
C | T | 9 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(6): Show | 9 | HG02602.hp1 HG03239.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-5353C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298824 | ||||||
chr5:298832
|
CCCCCGCA others(6): Show |
C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-5340_164-5328d others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298832 | |||||
chr5:298836
|
C | T | 70 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-5341C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298836 | ||||||
chr5:298837
|
G | C | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(6): Show | 9 | HG02922.hp1 HG03139.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-5340G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298837 | ||||||
chr5:298838
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-5339C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298838 | ||||||
chr5:298843
|
G | A | 70 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-5334G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298843 | ||||||
chr5:298846
|
CCCCCCAG others(5): Show |
C | 1 | a0001c0002t0001g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.164-5315_164-5304d others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 298846 | |||||
chr5:298850
|
C | CG | 5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | NA18950.hp1 NA18957.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-5327_164-5326i others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298850 | ||||||
chr5:298991
|
T | C | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-5186T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 298991 | ||||||
chr5:299009
|
CCTCCCCA others(20): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164-5166_164-5140d others(29): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299009 | |||||
chr5:299011
|
T | TCCCTAGC others(6): Show |
1 | a0002c0003t0001g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.164-5163_164-5162i others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299011 | |||||
chr5:299011
|
T | TCCCTAGC others(7): Show |
31 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(28): Show | 31 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-5163_164-5162i others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299011 | |||||
chr5:299011
|
T | TCCCTAGC others(21): Show |
7 | a0002c0004t0003g0279a0003c0005t0004g0020a0003c0005t0004g0305others(4): Show | 8 | HG01099.hp2 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-5163_164-5162i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299011 | |||||
chr5:299015
|
C | T | 32 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(29): Show | 34 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.164-5162C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299015 | ||||||
chr5:299023
|
CCCCCCCA others(6): Show |
C | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.164-5144_164-5132d others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299023 | |||||
chr5:299033
|
C | T | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0143others(91): Show | 99 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.164-5144C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299033 | ||||||
chr5:299046
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.164-5131T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299046 | ||||||
chr5:299049
|
T | TCCCCCCA others(7): Show |
1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.164-5116_164-5103d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299049 | |||||
chr5:299049
|
T | TCCCCCCC others(8): Show |
20 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(17): Show | 21 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-5122_164-5121i others(17): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299049 | |||||
chr5:299049
|
T | TCCCCCCC others(48): Show |
3 | a0001c0001t0002g0069a0001c0001t0002g0071a0001c0001t0003g0070 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.164-5122_164-5121i others(57): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299049 | |||||
chr5:299050
|
CCCCCCAG others(5): Show |
C | 1 | a0001c0001t0001g0234 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.164-5121_164-5110d others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299050 | |||||
chr5:299059
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-5118T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299059 | ||||||
chr5:299070
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-5107A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299070 | ||||||
chr5:299074
|
G | GCTCCCCC others(46): Show |
5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5103_164-5102i others(55): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299074 | ||||||
chr5:299075
|
T | C | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-5102T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299075 | ||||||
chr5:299076
|
T | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5101T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299076 | ||||||
chr5:299080
|
A | C | 6 | a0001c0001t0003g0310a0001c0001t0005g0019a0001c0001t0005g0270others(3): Show | 7 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-5097A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299080 | ||||||
chr5:299080
|
ACCCAGCT others(7): Show |
A | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(15): Show | 20 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.164-5057_164-5044d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299080 | |||||
chr5:299090
|
TC | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 94 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.164-5080delC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299090 | |||||
chr5:299090
|
TCCCCCCC others(8): Show |
T | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | NA18950.hp1 NA18957.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-5080_164-5066d others(17): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299090 | |||||
chr5:299094
|
C | CCCCAGCT others(61): Show |
1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-5072_164-5071i others(70): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299094 | |||||
chr5:299094
|
C | CCCCCAGC others(35): Show |
1 | a0002c0003t0001g0293 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-5080_164-5079i others(44): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299094 | |||||
chr5:299104
|
TC | T | 64 | a0001c0001t0001g0188a0001c0001t0002g0008a0001c0001t0002g0065others(61): Show | 66 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.164-5066delC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299104 | |||||
chr5:299106
|
C | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5071C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299106 | ||||||
chr5:299108
|
C | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-5069C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299108 | ||||||
chr5:299124
|
C | T | 2 | a0001c0001t0003g0310a0002c0003t0001g0293 | 2 | HG01978.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164-5053C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299124 | ||||||
chr5:299134
|
T | C | 7 | a0001c0001t0003g0310a0001c0001t0005g0019a0001c0001t0005g0270others(4): Show | 8 | HG01978.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-5043T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299134 | ||||||
chr5:299137
|
C | CCCAGCTG others(35): Show |
64 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(61): Show | 66 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.164-5023_164-5022i others(44): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299137 | |||||
chr5:299137
|
C | T | 7 | a0001c0001t0003g0310a0001c0001t0005g0019a0001c0001t0005g0270others(4): Show | 8 | HG01978.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-5040C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299137 | ||||||
chr5:299192
|
A | C | 70 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-4985A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299192 | ||||||
chr5:299206
|
C | CT | 5 | a0001c0002t0001g0053a0001c0002t0001g0136a0001c0002t0001g0316others(2): Show | 5 | HG02056.hp2 HG02071.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-4971_164-4970i others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299206 | ||||||
chr5:299208
|
A | C | 5 | a0001c0002t0001g0053a0001c0002t0001g0136a0001c0002t0001g0316others(2): Show | 5 | HG02056.hp2 HG02071.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-4969A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299208 | ||||||
chr5:299240
|
CTCCCCCC others(7): Show |
C | 1 | a0001c0002t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.164-4920_164-4907d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299240 | |||||
chr5:299244
|
C | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(88): Show | 95 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.164-4933C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299244 | ||||||
chr5:299260
|
C | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-4917C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299260 | ||||||
chr5:299322
|
G | A | 67 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(64): Show | 70 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.164-4855G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299322 | ||||||
chr5:299352
|
CAA | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.164-4823_164-4822d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299352 | |||||
chr5:299417
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-4760T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299417 | ||||||
chr5:299428
|
C | T | 41 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(38): Show | 42 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-4749C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299428 | ||||||
chr5:299446
|
C | T | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-4731C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299446 | ||||||
chr5:299456
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-4721C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299456 | ||||||
chr5:299506
|
T | C | 41 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(38): Show | 42 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-4671T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299506 | ||||||
chr5:299551
|
G | GT | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0143others(45): Show | 51 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.164-4614dupT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299551 | |||||
chr5:299551
|
G | GTT | 6 | a0001c0001t0001g0168a0001c0001t0005g0019a0001c0001t0005g0270others(3): Show | 7 | HG01515.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-4615_164-4614d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299551 | |||||
chr5:299558
|
T | TC | 31 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(28): Show | 32 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.164-4619_164-4618i others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299558 | ||||||
chr5:299575
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.164-4602A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299575 | ||||||
chr5:299584
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-4593T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299584 | ||||||
chr5:299589
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-4588G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299589 | ||||||
chr5:299603
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.164-4574C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299603 | ||||||
chr5:299610
|
T | C | 2 | a0001c0001t0001g0199a0002c0003t0001g0284 | 2 | HG01943.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.164-4567T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299610 | ||||||
chr5:299613
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.164-4564A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299613 | ||||||
chr5:299619
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02683.hp1 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-4558A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299619 | ||||||
chr5:299636
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.164-4541A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299636 | ||||||
chr5:299642
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00741.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.164-4535C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299642 | ||||||
chr5:299687
|
C | T | 8 | a0001c0001t0001g0167a0001c0001t0001g0244a0002c0003t0001g0288others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-4490C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299687 | ||||||
chr5:299689
|
A | G | 1 | a0001c0001t0006g0204 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.164-4488A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299689 | ||||||
chr5:299695
|
A | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0230a0001c0001t0001g0245others(3): Show | 6 | HG00597.hp2 NA18941.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-4482A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299695 | ||||||
chr5:299697
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.164-4480A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299697 | ||||||
chr5:299702
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.164-4475G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299702 | ||||||
chr5:299706
|
T | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0188others(3): Show | 6 | HG02559.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-4471T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299706 | ||||||
chr5:299708
|
C | A | 1 | a0001c0001t0001g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.164-4469C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299708 | ||||||
chr5:299739
|
T | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0160a0001c0001t0001g0166others(10): Show | 13 | HG00597.hp2 HG00609.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-4438T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299739 | ||||||
chr5:299742
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.164-4435G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299742 | ||||||
chr5:299750
|
C | T | 8 | a0001c0001t0002g0071a0001c0002t0001g0131a0002c0004t0003g0279others(5): Show | 9 | HG01099.hp2 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-4427C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299750 | ||||||
chr5:299751
|
A | G | 5 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0224others(2): Show | 5 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-4426A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299751 | ||||||
chr5:299753
|
A | G | 70 | a0001c0001t0001g0021a0001c0001t0001g0171a0001c0001t0001g0175others(67): Show | 72 | HG00140.hp2 HG00544.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.164-4424A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299753 | ||||||
chr5:299779
|
C | G | 10 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-4398C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299779 | ||||||
chr5:299784
|
G | C | 10 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-4393G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299784 | ||||||
chr5:299795
|
C | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-4382C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299795 | ||||||
chr5:299800
|
T | C | 8 | a0001c0001t0001g0175a0001c0001t0005g0019a0001c0001t0005g0270others(5): Show | 9 | HG00099.hp1 HG01975.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-4377T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299800 | ||||||
chr5:299845
|
A | G | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(2): Show | 5 | HG02818.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-4332A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299845 | ||||||
chr5:299852
|
A | AT | 45 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(42): Show | 48 | HG00558.hp2 HG01099.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.164-4314dupT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299852 | |||||
chr5:299852
|
A | ATT | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(14): Show | 19 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.164-4315_164-4314d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 299852 | |||||
chr5:299856
|
T | A | 1 | a0002c0003t0001g0288 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-4321T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299856 | ||||||
chr5:299864
|
A | G | 36 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(33): Show | 39 | HG01099.hp2 HG01243.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.164-4313A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299864 | ||||||
chr5:299864
|
A | T | 1 | a0002c0003t0001g0286 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164-4313A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299864 | ||||||
chr5:299866
|
T | A | 1 | a0002c0003t0001g0286 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164-4311T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299866 | ||||||
chr5:299903
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-4274A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299903 | ||||||
chr5:299945
|
T | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.164-4232T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299945 | ||||||
chr5:299958
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.164-4219A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299958 | ||||||
chr5:299972
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.164-4205G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299972 | ||||||
chr5:299990
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.164-4187T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 299990 | ||||||
chr5:300026
|
A | G | 80 | a0001c0001t0001g0170a0001c0001t0002g0008a0001c0001t0002g0065others(77): Show | 83 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-4151A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300026 | ||||||
chr5:300073
|
G | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.164-4104G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300073 | ||||||
chr5:300135
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.164-4042C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300135 | ||||||
chr5:300139
|
T | C | 275 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.164-4038T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300139 | ||||||
chr5:300140
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-4037G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300140 | ||||||
chr5:300335
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.164-3842C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300335 | ||||||
chr5:300353
|
C | T | 70 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(67): Show | 73 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.164-3824C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300353 | ||||||
chr5:300373
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.164-3804C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300373 | ||||||
chr5:300395
|
G | A | 27 | a0001c0002t0001g0003a0001c0002t0001g0053a0001c0002t0001g0136others(24): Show | 29 | HG00609.hp2 HG01109.hp2 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.164-3782G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300395 | ||||||
chr5:300644
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-3533A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300644 | ||||||
chr5:300676
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.164-3501C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300676 | ||||||
chr5:300786
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-3391C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 300786 | ||||||
chr5:301073
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.164-3104G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301073 | ||||||
chr5:301138
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-3039G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301138 | ||||||
chr5:301177
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.164-3000C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301177 | ||||||
chr5:301215
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-2962C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301215 | ||||||
chr5:301328
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(68): Show | 74 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164-2849G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301328 | ||||||
chr5:301441
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.164-2736T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301441 | ||||||
chr5:301487
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.164-2690A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301487 | ||||||
chr5:301494
|
T | C | 1 | a0002c0003t0001g0295 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.164-2683T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301494 | ||||||
chr5:301573
|
C | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2604C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301573 | ||||||
chr5:301578
|
G | A | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2599G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301578 | ||||||
chr5:301584
|
C | G | 34 | a0002c0003t0001g0274a0002c0003t0001g0277a0002c0003t0001g0278others(31): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.164-2593C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301584 | ||||||
chr5:301603
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.164-2574A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301603 | ||||||
chr5:301604
|
T | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.164-2573T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301604 | ||||||
chr5:301608
|
T | TCAGGTTC others(1187): Show |
1 | a0001c0002t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-2506_164-1313d others(1196): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 301608 | |||||
chr5:301765
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.164-2412G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301765 | ||||||
chr5:301772
|
G | A | 1 | a0002c0003t0001g0299 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.164-2405G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301772 | ||||||
chr5:301947
|
G | T | 30 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(27): Show | 32 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.164-2230G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301947 | ||||||
chr5:301967
|
G | A | 2 | a0001c0001t0002g0075a0001c0002t0001g0044 | 2 | HG02818.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.164-2210G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301967 | ||||||
chr5:301975
|
G | C | 1 | a0001c0001t0005g0272 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.164-2202G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301975 | ||||||
chr5:301989
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.164-2188C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 301989 | ||||||
chr5:302070
|
C | CTG | 51 | a0001c0001t0001g0093a0001c0001t0001g0143a0001c0001t0001g0201others(48): Show | 53 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.164-2070_164-2069d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTG | 16 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0001g0193others(13): Show | 16 | HG00597.hp2 HG02056.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-2072_164-2069d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTG | 6 | a0001c0001t0001g0144a0001c0001t0001g0247a0001c0001t0001g0257others(3): Show | 6 | HG01192.hp1 HG02071.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2074_164-2069d others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(1): Show |
8 | a0001c0001t0001g0190a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 8 | HG01175.hp1 HG01261.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-2076_164-2069d others(10): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(3): Show |
13 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0001g0231others(10): Show | 14 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-2078_164-2069d others(12): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(5): Show |
10 | a0001c0001t0001g0023a0001c0001t0001g0188a0001c0001t0001g0200others(7): Show | 10 | HG00140.hp1 HG02148.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-2080_164-2069d others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(7): Show |
23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(20): Show | 25 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.164-2082_164-2069d others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(9): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0179others(5): Show | 9 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-2084_164-2069d others(18): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(11): Show |
14 | a0001c0001t0001g0016a0001c0001t0001g0180a0001c0001t0001g0181others(11): Show | 15 | HG00733.hp1 HG01256.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-2086_164-2069d others(20): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(13): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0192a0001c0001t0001g0199others(1): Show | 4 | HG01943.hp1 NA18747.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-2088_164-2069d others(22): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.164-2090_164-2069d others(24): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
CTG | C | 10 | a0001c0001t0002g0072a0001c0001t0002g0074a0001c0001t0002g0075others(7): Show | 10 | HG01978.hp2 HG02040.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-2070_164-2069d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
CTGTG | C | 17 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(14): Show | 17 | HG02145.hp1 HG02273.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-2072_164-2069d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
CTGTGTG | C | 6 | a0001c0001t0001g0175a0001c0001t0002g0008a0001c0001t0002g0066others(3): Show | 7 | HG02145.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-2074_164-2069d others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
CTGTGTGT others(5): Show |
C | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-2080_164-2069d others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302070
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.164-2090_164-2069d others(24): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302070 | |||||
chr5:302080
|
G | GTGTC | 11 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-2094_164-2093i others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302080 | |||||
chr5:302084
|
G | C | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2093G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302084 | ||||||
chr5:302107
|
T | C | 37 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(34): Show | 38 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.164-2070T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302107 | ||||||
chr5:302107
|
T | TGC | 9 | a0001c0001t0002g0068a0001c0002t0001g0043a0001c0002t0001g0046others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-2069_164-2068d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGCGC | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2068_164-2067i others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGCGC | 2 | a0001c0001t0005g0019a0001c0001t0005g0270 | 3 | HG03471.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.164-2069_164-2068i others(8): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0005g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.164-2069_164-2068i others(12): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0005g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.164-2069_164-2068i others(14): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0196 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.164-2069_164-2068i others(16): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0232 | 2 | HG01106.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.164-2069_164-2068i others(18): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302107
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.164-2069_164-2068i others(20): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302107 | |||||
chr5:302180
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.164-1997G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302180 | ||||||
chr5:302191
|
C | CTG | 8 | a0001c0002t0001g0053a0001c0002t0001g0108a0001c0002t0001g0110others(5): Show | 8 | HG00544.hp1 HG01074.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-1966_164-1965d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302191 | |||||
chr5:302191
|
CTG | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.164-1966_164-1965d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302191 | |||||
chr5:302191
|
CTGTGTGT others(297): Show |
C | 1 | a0001c0001t0001g0193 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.164-1966_164-1663d others(2): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302191 | |||||
chr5:302246
|
T | G | 4 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | NA18957.hp2 NA18992.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-1931T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302246 | ||||||
chr5:302329
|
C | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.164-1848C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302329 | ||||||
chr5:302345
|
GGCACAGC others(88): Show |
G | 2 | a0001c0001t0001g0243a0001c0001t0001g0260 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.164-1801_164-1707d others(97): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302345 | |||||
chr5:302382
|
GTGGAGTG others(88): Show |
G | 47 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(44): Show | 50 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.164-1782_164-1688d others(97): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302382 | |||||
chr5:302393
|
CTCTGTGT others(82): Show |
C | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1782_164-1694d others(91): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302393 | |||||
chr5:302395
|
CTGTGTGT others(105): Show |
C | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(9): Show | 14 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-1767_164-1656d others(2): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302395 | |||||
chr5:302410
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.164-1767A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302410 | ||||||
chr5:302491
|
C | CTG | 22 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(19): Show | 23 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-1664_164-1663d others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302491 | |||||
chr5:302491
|
C | CTGTG | 26 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(23): Show | 27 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.164-1666_164-1663d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302491 | |||||
chr5:302491
|
CTGTG | C | 18 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(15): Show | 19 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-1666_164-1663d others(6): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 302491 | |||||
chr5:302652
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.164-1525A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302652 | ||||||
chr5:302663
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.164-1514A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302663 | ||||||
chr5:302711
|
C | T | 4 | a0001c0002t0001g0137a0001c0002t0001g0326a0001c0002t0001g0327others(1): Show | 4 | HG01109.hp2 HG01952.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-1466C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302711 | ||||||
chr5:302940
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.164-1237C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302940 | ||||||
chr5:302963
|
G | A | 1 | a0001c0001t0005g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.164-1214G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302963 | ||||||
chr5:302995
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-1182G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302995 | ||||||
chr5:302995
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.164-1182G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 302995 | ||||||
chr5:303011
|
T | A | 1 | a0001c0002t0001g0320 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.164-1166T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303011 | ||||||
chr5:303036
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-1141G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303036 | ||||||
chr5:303038
|
A | AC | 5 | a0001c0001t0001g0208a0001c0001t0001g0225a0001c0001t0002g0065others(2): Show | 5 | HG00738.hp1 HG01175.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-1134dupC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303038 | |||||
chr5:303223
|
A | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.164-954A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303223 | ||||||
chr5:303297
|
T | TA | 19 | a0001c0001t0001g0021a0001c0001t0001g0242a0001c0001t0001g0255others(16): Show | 20 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.164-865dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303297 | |||||
chr5:303297
|
T | TAA | 6 | a0001c0001t0002g0083a0001c0001t0003g0310a0001c0001t0005g0019others(3): Show | 7 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-866_164-865dup others(2): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303297 | |||||
chr5:303297
|
T | TAAA | 28 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(25): Show | 30 | HG01099.hp2 HG01261.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.164-867_164-865dup others(3): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303297 | |||||
chr5:303297
|
T | TAAAA | 11 | a0001c0001t0002g0065a0002c0004t0003g0265a0002c0004t0003g0266others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-868_164-865dup others(4): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303297 | |||||
chr5:303297
|
TA | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(10): Show | 15 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.164-865delA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 303297 | |||||
chr5:303325
|
C | T | 1 | a0001c0001t0001g0211 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.164-852C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303325 | ||||||
chr5:303331
|
C | T | 49 | a0001c0001t0001g0211a0001c0001t0002g0008a0001c0001t0002g0065others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.164-846C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303331 | ||||||
chr5:303449
|
C | T | 1 | a0002c0003t0001g0288 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-728C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303449 | ||||||
chr5:303541
|
C | G | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(4): Show | 7 | HG02056.hp2 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-636C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303541 | ||||||
chr5:303570
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.164-607C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303570 | ||||||
chr5:303571
|
A | G | 49 | a0001c0001t0001g0238a0001c0001t0002g0008a0001c0001t0002g0065others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.164-606A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303571 | ||||||
chr5:303603
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.164-574G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303603 | ||||||
chr5:303663
|
C | T | 11 | a0001c0001t0001g0158a0001c0001t0001g0214a0001c0001t0001g0223others(8): Show | 13 | HG00673.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-514C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303663 | ||||||
chr5:303733
|
T | C | 49 | a0001c0001t0001g0220a0001c0001t0002g0008a0001c0001t0002g0065others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.164-444T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303733 | ||||||
chr5:303735
|
C | T | 48 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.164-442C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303735 | ||||||
chr5:303759
|
C | T | 36 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(33): Show | 39 | HG01099.hp2 HG01261.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.164-418C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303759 | ||||||
chr5:303789
|
C | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-388C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303789 | ||||||
chr5:303797
|
C | T | 48 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.164-380C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303797 | ||||||
chr5:303859
|
T | C | 49 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.164-318T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303859 | ||||||
chr5:303888
|
T | C | 42 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(39): Show | 44 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.164-289T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303888 | ||||||
chr5:303908
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0217 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.164-269G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303908 | ||||||
chr5:303924
|
G | A | 43 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(40): Show | 45 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.164-253G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303924 | ||||||
chr5:303937
|
G | A | 9 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(6): Show | 9 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-240G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303937 | ||||||
chr5:303961
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-216G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303961 | ||||||
chr5:303990
|
A | C | 43 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0008others(40): Show | 45 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.164-187A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303990 | ||||||
chr5:303993
|
C | T | 1 | a0002c0003t0001g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-184C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 303993 | ||||||
chr5:304046
|
C | T | 2 | a0002c0003t0001g0301a0002c0003t0001g0303 | 2 | NA18965.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.164-131C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 304046 | ||||||
chr5:304071
|
T | C | 58 | a0001c0001t0001g0167a0001c0001t0001g0220a0001c0001t0001g0233others(55): Show | 61 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.164-106T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | 304071 | ||||||
chr5:304347
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(13): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+126C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304347 | ||||||
chr5:304371
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.208+150T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304371 | ||||||
chr5:304373
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.208+152C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304373 | ||||||
chr5:304392
|
A | G | 49 | a0001c0001t0001g0194a0001c0001t0002g0008a0001c0001t0002g0065others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.208+171A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304392 | ||||||
chr5:304463
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0223 | 2 | HG02148.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.208+242G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304463 | ||||||
chr5:304550
|
G | A | 2 | a0001c0002t0001g0321a0001c0002t0001g0322 | 2 | HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.208+329G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304550 | ||||||
chr5:304690
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.208+469G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304690 | ||||||
chr5:304928
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+707G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 304928 | ||||||
chr5:305072
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.208+851A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305072 | ||||||
chr5:305480
|
T | C | 30 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(27): Show | 32 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.209-1122T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305480 | ||||||
chr5:305624
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.209-978T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305624 | ||||||
chr5:305676
|
C | CA | 4 | a0002c0004t0003g0280a0002c0004t0003g0281a0002c0004t0003g0282others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-925dupA | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 305676 | |||||
chr5:305689
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.209-913G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305689 | ||||||
chr5:305725
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.209-877A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305725 | ||||||
chr5:305738
|
C | T | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-864C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305738 | ||||||
chr5:305799
|
T | A | 1 | a0002c0004t0003g0298 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.209-803T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305799 | ||||||
chr5:305868
|
A | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.209-734A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305868 | ||||||
chr5:305917
|
G | A | 42 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(39): Show | 44 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.209-685G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 305917 | ||||||
chr5:306070
|
G | A | 5 | a0002c0003t0001g0288a0002c0003t0001g0289a0002c0003t0001g0291others(2): Show | 5 | HG00140.hp2 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-532G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 306070 | ||||||
chr5:306198
|
C | T | 2 | a0001c0002t0001g0013a0001c0002t0001g0145 | 3 | HG01891.hp1 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.209-404C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 306198 | ||||||
chr5:306568
|
T | C | 24 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-34T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 306568 | ||||||
chr5:306585
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-17G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 3/5 | chr5 | 306585 | ||||||
chr5:306866
|
C | T | 18 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(15): Show | 19 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.367+106C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 306866 | ||||||
chr5:306913
|
A | G | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367+153A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 306913 | ||||||
chr5:306943
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.367+183G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 306943 | ||||||
chr5:307162
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+402A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307162 | ||||||
chr5:307170
|
ACCGTGCG others(101): Show |
A | 27 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(24): Show | 28 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.367+495_367+602del | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307170 | |||||
chr5:307176
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.367+416C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307176 | ||||||
chr5:307218
|
GGTGTGCT others(8): Show |
G | 7 | a0002c0003t0001g0286a0002c0003t0001g0288a0002c0003t0001g0289others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+495_367+509del others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307218 | |||||
chr5:307233
|
TGTGTGCT others(86): Show |
T | 115 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.367+570_367+662del others(93): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307233 | |||||
chr5:307235
|
TGTGCTCG others(84): Show |
T | 1 | a0001c0001t0001g0247 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.367+479_367+569del others(91): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307235 | |||||
chr5:307241
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.367+481C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307241 | ||||||
chr5:307243
|
GCGTGTGT others(115): Show |
G | 24 | a0001c0001t0003g0310a0001c0001t0005g0019a0001c0001t0005g0270others(21): Show | 26 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.367+490_367+611del | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307243 | |||||
chr5:307246
|
TGTGTGTG others(84): Show |
T | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.367+494_367+584del others(91): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307246 | |||||
chr5:307285
|
G | A | 7 | a0001c0002t0001g0024a0001c0002t0001g0043a0001c0002t0001g0060others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+525G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307285 | ||||||
chr5:307326
|
GGTGTGCT others(8): Show |
G | 2 | a0001c0002t0001g0102a0001c0002t0001g0115 | 2 | HG01496.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.367+588_367+602del others(15): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 307326 | |||||
chr5:307333
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.367+573T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307333 | ||||||
chr5:307334
|
C | T | 12 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(9): Show | 12 | HG00733.hp1 HG01175.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+574C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307334 | ||||||
chr5:307335
|
G | A | 4 | a0001c0002t0001g0105a0001c0002t0001g0109a0001c0002t0001g0118others(1): Show | 4 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+575G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307335 | ||||||
chr5:307398
|
C | T | 22 | a0001c0002t0001g0003a0001c0002t0001g0053a0001c0002t0001g0136others(19): Show | 24 | HG00609.hp2 HG02056.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.367+638C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307398 | ||||||
chr5:307405
|
C | T | 3 | a0002c0003t0001g0288a0002c0003t0001g0289a0002c0003t0007g0287 | 3 | HG00733.hp2 HG01074.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.367+645C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307405 | ||||||
chr5:307428
|
A | G | 1 | a0001c0002t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.367+668A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307428 | ||||||
chr5:307463
|
T | C | 1 | a0001c0002t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.367+703T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307463 | ||||||
chr5:307518
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.367+758C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307518 | ||||||
chr5:307526
|
C | T | 12 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+766C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307526 | ||||||
chr5:307647
|
A | T | 1 | a0001c0002t0001g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.367+887A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307647 | ||||||
chr5:307733
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.367+973C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307733 | ||||||
chr5:307749
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367+989C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307749 | ||||||
chr5:307798
|
G | A | 6 | a0001c0001t0002g0074a0001c0001t0005g0019a0001c0001t0005g0270others(3): Show | 7 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+1038G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307798 | ||||||
chr5:307865
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0224 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.367+1105G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307865 | ||||||
chr5:307927
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | NA18987.hp1 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.367+1167C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 307927 | ||||||
chr5:308073
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.367+1313C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308073 | ||||||
chr5:308138
|
C | T | 1 | a0002c0003t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.367+1378C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308138 | ||||||
chr5:308153
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(97): Show | 103 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.367+1393C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308153 | ||||||
chr5:308178
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.367+1418C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308178 | ||||||
chr5:308189
|
G | A | 1 | a0001c0002t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.367+1429G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308189 | ||||||
chr5:308237
|
T | C | 41 | a0001c0001t0001g0263a0001c0001t0002g0008a0001c0001t0002g0065others(38): Show | 44 | HG00099.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.367+1477T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308237 | ||||||
chr5:308319
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.367+1559G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308319 | ||||||
chr5:308366
|
C | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 5 | HG02145.hp2 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+1606C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308366 | ||||||
chr5:308786
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.367+2026G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308786 | ||||||
chr5:308941
|
C | T | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+2181C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308941 | ||||||
chr5:308945
|
A | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.367+2185A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308945 | ||||||
chr5:308960
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.367+2200C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308960 | ||||||
chr5:308966
|
G | T | 1 | a0001c0001t0002g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.367+2206G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308966 | ||||||
chr5:308981
|
A | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.367+2221A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 308981 | ||||||
chr5:309184
|
G | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-2109G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309184 | ||||||
chr5:309197
|
C | G | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-2096C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309197 | ||||||
chr5:309220
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.368-2073C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309220 | ||||||
chr5:309290
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-2003G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309290 | ||||||
chr5:309368
|
T | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0082others(1): Show | 4 | HG01261.hp2 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1925T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309368 | ||||||
chr5:309370
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.368-1923G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309370 | ||||||
chr5:309504
|
C | CTGCCTCT others(147): Show |
1 | a0001c0001t0002g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.368-1771_368-1770i others(156): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309504 | |||||
chr5:309566
|
T | TGTCCCCA others(329): Show |
1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.368-1721_368-1720i others(338): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCC others(217): Show |
1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.368-1721_368-1720i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(217): Show |
2 | a0001c0002t0001g0032a0001c0002t0001g0042 | 2 | HG02083.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(245): Show |
1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(254): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(469): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(478): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(49): Show |
9 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(6): Show | 9 | HG01081.hp2 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.368-1718_368-1717i others(58): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(77): Show |
1 | a0001c0001t0005g0272 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.368-1718_368-1717i others(86): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(161): Show |
1 | a0002c0004t0003g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.368-1718_368-1717i others(170): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(329): Show |
1 | a0002c0004t0003g0298 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.368-1718_368-1717i others(338): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(581): Show |
1 | a0001c0001t0005g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.368-1718_368-1717i others(590): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(553): Show |
1 | a0001c0001t0005g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.368-1718_368-1717i others(562): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(609): Show |
2 | a0001c0001t0005g0019a0001c0001t0005g0271 | 3 | HG02647.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.368-1718_368-1717i others(618): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCCG others(525): Show |
1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1718_368-1717i others(534): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
T | TGTCCCGT others(160): Show |
1 | a0001c0001t0002g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.368-1722_368-1721i others(169): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309566
|
TGTCCCCG others(161): Show |
T | 1 | a0002c0003t0001g0293 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.368-1658_368-1491d others(2): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309566 | |||||
chr5:309576
|
C | T | 29 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(26): Show | 31 | HG01099.hp2 HG01261.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.368-1717C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309576 | ||||||
chr5:309579
|
C | A | 5 | a0001c0001t0003g0310a0001c0001t0005g0019a0001c0001t0005g0270others(2): Show | 6 | HG00735.hp1 HG02647.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-1714C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309579 | ||||||
chr5:309579
|
C | CCCAGTGA others(216): Show |
1 | a0001c0002t0001g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.368-1685_368-1684i others(225): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(217): Show |
1 | a0001c0001t0001g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(217): Show |
3 | a0001c0002t0001g0122a0001c0002t0001g0130a0001c0002t0001g0140 | 3 | HG00099.hp1 HG02040.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(189): Show |
10 | a0001c0002t0001g0034a0001c0002t0001g0091a0001c0002t0001g0123others(7): Show | 10 | HG00642.hp2 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(198): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(637): Show |
1 | a0001c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(646): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(218): Show |
1 | a0001c0002t0001g0060 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(227): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(385): Show |
1 | a0001c0002t0001g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(394): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(217): Show |
1 | a0001c0002t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(217): Show |
118 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0005others(115): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309579
|
C | CCCAGTGA others(245): Show |
3 | a0001c0002t0001g0002a0001c0002t0001g0087a0001c0002t0001g0104 | 5 | NA18980.hp2 NA19012.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(254): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309579 | |||||
chr5:309587
|
T | G | 5 | a0001c0001t0002g0071a0001c0001t0002g0080a0001c0001t0003g0310others(2): Show | 5 | HG02257.hp1 NA19012.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1706T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309587 | ||||||
chr5:309587
|
T | TGGCCGCC others(217): Show |
6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-1699_368-1698i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309587
|
T | TGGCCGCC others(161): Show |
1 | a0001c0002t0001g0153 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(170): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309587
|
T | TGGCCGCC others(189): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0188others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(198): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309587
|
T | TGGCCGCC others(329): Show |
1 | a0001c0001t0001g0201 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(338): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309587
|
T | TGGCCGCC others(553): Show |
2 | a0001c0001t0001g0214a0001c0001t0001g0223 | 2 | HG02148.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(562): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309587
|
TGGCCGCC others(133): Show |
T | 1 | a0001c0002t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.368-1658_368-1519d others(2): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309587 | |||||
chr5:309595
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-1698G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309595 | ||||||
chr5:309607
|
C | A | 10 | a0001c0001t0001g0183a0002c0004t0003g0265a0002c0004t0003g0266others(7): Show | 10 | HG01081.hp2 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-1686C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309607 | ||||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
1 | a0001c0001t0001g0259 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
1 | a0001c0001t0001g0247 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(161): Show |
2 | a0002c0003t0001g0295a0002c0003t0001g0296 | 2 | HG01975.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(170): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
1 | a0001c0001t0001g0216 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(189): Show |
14 | a0001c0001t0001g0328a0001c0002t0001g0038a0001c0002t0001g0044others(11): Show | 14 | HG00438.hp2 HG01106.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(198): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
1 | a0001c0002t0001g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(441): Show |
1 | a0001c0001t0001g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(450): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
1 | a0001c0001t0001g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(217): Show |
77 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 80 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(189): Show |
1 | a0001c0001t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(198): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(469): Show |
10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0161others(7): Show | 12 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(478): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(385): Show |
1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(394): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309607
|
C | CCCAGTGA others(301): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0209 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(310): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309607 | |||||
chr5:309615
|
T | G | 19 | a0001c0001t0002g0080a0001c0001t0003g0310a0002c0004t0002g0269others(16): Show | 20 | HG01081.hp2 HG01099.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.368-1678T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309615 | ||||||
chr5:309615
|
T | TGGCCGCC others(49): Show |
1 | a0002c0004t0003g0268 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.368-1659_368-1658i others(58): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(1057): Show |
2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(1066): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(1057): Show |
1 | a0001c0001t0002g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(1066): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(105): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0149 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(114): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(133): Show |
1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(142): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(217): Show |
6 | a0002c0003t0001g0284a0002c0003t0001g0300a0002c0003t0001g0301others(3): Show | 6 | HG02015.hp2 HG02132.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(245): Show |
1 | a0001c0002t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(254): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(217): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0337 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(226): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309615
|
T | TGGCCGCC others(273): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.368-1659_368-1658i others(282): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309615 | |||||
chr5:309624
|
T | TCCCCGTG others(218): Show |
1 | a0001c0001t0001g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.368-1659_368-1658i others(227): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309624 | |||||
chr5:309635
|
A | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0144others(68): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.368-1658A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309635 | ||||||
chr5:309643
|
G | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(63): Show | 70 | HG00280.hp1 HG00438.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.368-1650G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309643 | ||||||
chr5:309651
|
G | A | 1 | a0001c0002t0001g0311 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.368-1642G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309651 | ||||||
chr5:309663
|
A | C | 52 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(49): Show | 55 | HG01081.hp2 HG01099.hp2 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.368-1630A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309663 | ||||||
chr5:309671
|
G | T | 30 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(27): Show | 31 | HG01255.hp1 HG01261.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.368-1622G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309671 | ||||||
chr5:309683
|
C | T | 1 | a0001c0002t0001g0332 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.368-1610C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309683 | ||||||
chr5:309691
|
C | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(123): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.368-1602C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309691 | ||||||
chr5:309691
|
C | ACCAGTGA others(21): Show |
1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.368-1630_368-1603d others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309691 | ||||||
chr5:309699
|
G | GGGCCGCC others(21): Show |
1 | a0001c0001t0001g0004 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.368-1575_368-1574i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309699 | |||||
chr5:309699
|
G | GGGCCGCC others(21): Show |
7 | a0001c0001t0001g0176a0001c0001t0001g0212a0001c0002t0001g0034others(4): Show | 7 | HG01069.hp1 HG02602.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-1350_368-1323d others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309699 | |||||
chr5:309699
|
G | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0143others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.368-1594G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309699 | ||||||
chr5:309719
|
C | A | 14 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0214others(11): Show | 15 | HG01099.hp2 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.368-1574C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309719 | ||||||
chr5:309727
|
T | G | 45 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0205others(42): Show | 45 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.368-1566T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309727 | ||||||
chr5:309747
|
C | A | 6 | a0001c0001t0001g0261a0001c0001t0003g0310a0001c0001t0005g0019others(3): Show | 7 | HG02280.hp2 HG02647.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-1546C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309747 | ||||||
chr5:309747
|
C | CCCAGTGA others(273): Show |
1 | a0001c0001t0002g0084 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.368-1539_368-1538i others(282): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(666): Show |
1 | a0001c0001t0002g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.368-1539_368-1538i others(675): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(1029): Show |
2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.368-1539_368-1538i others(1038): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(525): Show |
3 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067 | 4 | HG02145.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1539_368-1538i others(534): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(1057): Show |
3 | a0001c0001t0002g0069a0001c0001t0002g0073a0001c0001t0003g0070 | 3 | HG02273.hp2 HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.368-1539_368-1538i others(1066): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(805): Show |
1 | a0001c0001t0002g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.368-1539_368-1538i others(814): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(1057): Show |
1 | a0001c0001t0002g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.368-1539_368-1538i others(1066): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309747
|
C | CCCAGTGA others(553): Show |
1 | a0001c0001t0002g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.368-1539_368-1538i others(562): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309747 | |||||
chr5:309755
|
T | G | 20 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(17): Show | 21 | HG01255.hp1 HG01261.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.368-1538T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309755 | ||||||
chr5:309755
|
T | TGGCCGCC others(469): Show |
1 | a0002c0004t0002g0269 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.368-1511_368-1510i others(478): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309755 | |||||
chr5:309755
|
T | TGGCCGCC others(693): Show |
1 | a0001c0001t0002g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.368-1511_368-1510i others(702): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309755 | |||||
chr5:309755
|
T | TGGCCGCC others(385): Show |
1 | a0001c0001t0001g0261 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.368-1492_368-1491i others(394): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309755 | |||||
chr5:309766
|
C | A | 12 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.368-1527C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309766 | ||||||
chr5:309775
|
C | A | 15 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 15 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.368-1518C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309775 | ||||||
chr5:309783
|
T | G | 4 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(1): Show | 5 | HG02280.hp2 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1510T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309783 | ||||||
chr5:309783
|
T | TGGCCGCC others(693): Show |
1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-1491_368-1490i others(702): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309783 | |||||
chr5:309783
|
T | TGGCCGCC others(1029): Show |
1 | a0001c0001t0002g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.368-1491_368-1490i others(1038): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309783 | |||||
chr5:309783
|
T | TGGCCGCC others(1030): Show |
1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.368-1427_368-1426i others(1039): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309783 | |||||
chr5:309783
|
T | TGGCCGCC others(1029): Show |
1 | a0001c0001t0002g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.368-1427_368-1426i others(1038): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309783 | |||||
chr5:309803
|
C | A | 1 | a0001c0001t0005g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.368-1490C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309803 | ||||||
chr5:309811
|
T | G | 3 | a0001c0001t0002g0071a0001c0001t0002g0076a0001c0001t0002g0077 | 3 | HG02809.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.368-1482T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309811 | ||||||
chr5:309820
|
T | TCCCCCGT others(23): Show |
1 | a0001c0001t0006g0204 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.368-1469_368-1468i others(32): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309820 | |||||
chr5:309831
|
C | CCCAGTGA others(105): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02886.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.368-1379_368-1378i others(114): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309831 | |||||
chr5:309839
|
T | G | 2 | a0001c0001t0002g0071a0001c0001t0002g0085 | 2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.368-1454T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309839 | ||||||
chr5:309843
|
C | T | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.368-1450C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309843 | ||||||
chr5:309867
|
T | G | 2 | a0001c0001t0002g0071a0001c0002t0001g0117 | 2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.368-1426T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309867 | ||||||
chr5:309895
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.368-1398T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309895 | ||||||
chr5:309923
|
T | G | 1 | a0001c0001t0002g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.368-1370T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309923 | ||||||
chr5:309943
|
C | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG02280.hp1 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1350C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309943 | ||||||
chr5:309943
|
C | CCCAGTGA others(21): Show |
88 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 92 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.368-1332_368-1305d others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309943 | |||||
chr5:309951
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.368-1342T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309951 | ||||||
chr5:309961
|
C | CCCCCGTG others(50): Show |
1 | a0001c0001t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.368-1329_368-1328i others(59): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309961 | |||||
chr5:309961
|
C | G | 6 | a0003c0005t0004g0020a0003c0005t0004g0305a0003c0005t0004g0306others(3): Show | 7 | HG01099.hp2 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-1332C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309961 | ||||||
chr5:309971
|
A | ACCAGTGA others(49): Show |
1 | a0001c0001t0001g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.368-1305_368-1304i others(58): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309971 | |||||
chr5:309971
|
A | ACCAGTGA others(21): Show |
1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368-1305_368-1304i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 309971 | |||||
chr5:309971
|
A | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(51): Show | 57 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.368-1322A>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309971 | ||||||
chr5:309979
|
T | G | 2 | a0001c0001t0002g0071a0001c0002t0001g0117 | 2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.368-1314T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309979 | ||||||
chr5:309989
|
G | C | 45 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(42): Show | 48 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.368-1304G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309989 | ||||||
chr5:309999
|
C | A | 48 | a0001c0001t0001g0206a0001c0001t0002g0008a0001c0001t0002g0065others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.368-1294C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 309999 | ||||||
chr5:310012
|
G | A | 4 | a0001c0001t0001g0176a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG00597.hp2 HG03704.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1281G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310012 | ||||||
chr5:310017
|
C | G | 47 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(44): Show | 50 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-1276C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310017 | ||||||
chr5:310018
|
C | CGGCCCAG others(740): Show |
1 | a0001c0001t0002g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.368-1275_368-1274i others(749): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310018 | ||||||
chr5:310027
|
A | ACCAGTGA others(21): Show |
1 | a0001c0001t0001g0206 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.368-1254_368-1253i others(30): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 310027 | |||||
chr5:310095
|
C | G | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1198C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310095 | ||||||
chr5:310098
|
T | G | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1195T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310098 | ||||||
chr5:310099
|
T | G | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1194T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310099 | ||||||
chr5:310101
|
T | G | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1192T>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310101 | ||||||
chr5:310104
|
G | C | 1 | a0001c0001t0002g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.368-1189G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310104 | ||||||
chr5:310183
|
C | A | 1 | a0001c0002t0001g0325 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.368-1110C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310183 | ||||||
chr5:310271
|
T | A | 30 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(27): Show | 32 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.368-1022T>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310271 | ||||||
chr5:310414
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.368-879C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310414 | ||||||
chr5:310415
|
G | A | 51 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(48): Show | 54 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.368-878G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310415 | ||||||
chr5:310510
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.368-783G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310510 | ||||||
chr5:310527
|
G | A | 1 | a0001c0002t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.368-766G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310527 | ||||||
chr5:310553
|
G | A | 1 | a0001c0002t0001g0334 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.368-740G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310553 | ||||||
chr5:310566
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.368-727C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310566 | ||||||
chr5:310727
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-566C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310727 | ||||||
chr5:310792
|
T | TTTGTATA others(12): Show |
1 | a0001c0001t0001g0247 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.368-488_368-487ins others(19): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 310792 | |||||
chr5:310834
|
GC | G | 23 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(20): Show | 24 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.368-458delC | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310834 | ||||||
chr5:310964
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.368-329G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310964 | ||||||
chr5:310996
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.368-297C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 310996 | ||||||
chr5:311141
|
C | T | 18 | a0002c0004t0003g0265a0002c0004t0003g0266a0002c0004t0003g0267others(15): Show | 19 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.368-152C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 311141 | ||||||
chr5:311193
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.368-100T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 4/5 | chr5 | 311193 | ||||||
chr5:311447
|
G | A | 48 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+45G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311447 | ||||||
chr5:311554
|
C | T | 48 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+152C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311554 | ||||||
chr5:311557
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.477+155T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311557 | ||||||
chr5:311722
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.477+320C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311722 | ||||||
chr5:311765
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(6): Show | 10 | HG00735.hp1 HG01081.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+363C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311765 | ||||||
chr5:311787
|
G | A | 37 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(34): Show | 40 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.477+385G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311787 | ||||||
chr5:311824
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477+422G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311824 | ||||||
chr5:311836
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0002t0001g0117 | 3 | HG02280.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.477+434G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311836 | ||||||
chr5:311847
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.477+445G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311847 | ||||||
chr5:311871
|
G | C | 1 | a0001c0001t0002g0084 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.477+469G>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311871 | ||||||
chr5:311916
|
C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 104 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.477+514C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311916 | ||||||
chr5:311981
|
G | A | 4 | a0001c0001t0005g0019a0001c0001t0005g0271a0001c0001t0005g0272others(1): Show | 5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+579G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 311981 | ||||||
chr5:312052
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.477+650A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312052 | ||||||
chr5:312065
|
G | A | 1 | a0001c0002t0001g0114 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.477+663G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312065 | ||||||
chr5:312138
|
G | A | 52 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(49): Show | 55 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.477+736G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312138 | ||||||
chr5:312235
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.477+833G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312235 | ||||||
chr5:312281
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.477+879C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312281 | ||||||
chr5:312334
|
C | G | 3 | a0001c0002t0001g0030a0001c0002t0001g0040a0001c0002t0001g0048 | 3 | HG00597.hp1 NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.477+932C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312334 | ||||||
chr5:312510
|
G | A | 48 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(45): Show | 51 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+1108G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312510 | ||||||
chr5:312556
|
T | C | 4 | a0001c0001t0002g0008a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 5 | HG02145.hp2 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+1154T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312556 | ||||||
chr5:312591
|
C | G | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+1189C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312591 | ||||||
chr5:312843
|
C | A | 49 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.477+1441C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312843 | ||||||
chr5:312855
|
CGTTCTGT others(36): Show |
C | 49 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.477+1500_478-1473d others(45): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 312855 | |||||
chr5:312874
|
C | T | 1 | a0002c0003t0001g0291 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.477+1472C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312874 | ||||||
chr5:312926
|
C | T | 3 | a0001c0001t0002g0066a0001c0001t0003g0064a0001c0001t0003g0310 | 3 | HG02818.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.478-1491C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312926 | ||||||
chr5:312952
|
A | G | 1 | a0001c0002t0001g0326 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.478-1465A>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 312952 | ||||||
chr5:313071
|
A | T | 19 | a0001c0001t0003g0070a0002c0004t0003g0265a0002c0004t0003g0266others(16): Show | 20 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-1346A>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313071 | ||||||
chr5:313222
|
C | G | 49 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 52 | HG00735.hp1 HG01081.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.478-1195C>G | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313222 | ||||||
chr5:313403
|
G | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0115 | 2 | HG01496.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.478-1014G>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313403 | ||||||
chr5:313467
|
G | GT | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(10): Show | 15 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.478-941dupT | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 313467 | |||||
chr5:313533
|
C | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-884C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313533 | ||||||
chr5:313564
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.478-853G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313564 | ||||||
chr5:313606
|
G | A | 5 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-811G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313606 | ||||||
chr5:313647
|
G | A | 167 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.478-770G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313647 | ||||||
chr5:313795
|
C | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.478-622C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313795 | ||||||
chr5:313896
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.478-521G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 313896 | ||||||
chr5:314030
|
C | CTGTGTCC others(3): Show |
146 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(143): Show | 152 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.478-387_478-386ins others(10): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314030 | ||||||
chr5:314030
|
C | CTGTGTCC others(4): Show |
1 | a0001c0001t0006g0229 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.478-387_478-386ins others(11): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314030 | ||||||
chr5:314051
|
C | A | 1 | a0002c0003t0001g0293 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.478-366C>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314051 | ||||||
chr5:314133
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149 | 3 | HG02922.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.478-284C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314133 | ||||||
chr5:314146
|
G | GAGACCAG others(73): Show |
1 | a0001c0002t0001g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.478-270_478-191dup others(80): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 314146 | |||||
chr5:314163
|
TCAGGGGC others(5): Show |
T | 3 | a0001c0001t0003g0064a0001c0001t0003g0310a0002c0003t0001g0284 | 3 | HG02818.hp1 NA18970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.478-236_478-225del others(12): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 314163 | |||||
chr5:314214
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(14): Show | 19 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.478-203C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314214 | ||||||
chr5:314231
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(91): Show | 98 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.478-186C>T | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314231 | ||||||
chr5:314232
|
G | A | 30 | a0001c0001t0001g0198a0001c0002t0001g0003a0001c0002t0001g0053others(27): Show | 32 | HG00609.hp2 HG02015.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.478-185G>A | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314232 | ||||||
chr5:314403
|
T | C | 52 | a0001c0001t0002g0008a0001c0001t0002g0065a0001c0001t0002g0066others(49): Show | 55 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.478-14T>C | PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 5/5 | chr5 | 314403 |