geneid | 51302 |
---|---|
ensemblid | ENSG00000146233.8 |
hgncid | 17449 |
symbol | CYP39A1 |
name | cytochrome P450 family 39 subfamily A member 1 |
refseq_nuc | NM_016593.5 |
refseq_prot | NP_057677.2 |
ensembl_nuc | ENST00000275016.3 |
ensembl_prot | ENSP00000275016.2 |
mane_status | MANE Select |
chr | chr6 |
start | 46549580 |
end | 46652818 |
strand | - |
ver | v1.2 |
region | chr6:46549580-46652818 |
region5000 | chr6:46544580-46657818 |
regionname0 | CYP39A1_chr6_46549580_46652818 |
regionname5000 | CYP39A1_chr6_46544580_46657818 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 469 | 114 | 47 | 9 | 43 | 3 | 12 | 37 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002 | 1/0 | 469 | 100 | 26 | 22 | 37 | 4 | 10 | 24 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0003 | 0/1 | 469 | 26 | 4 | 6 | 12 | 1 | 2 | 11 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0004 | 0/0 | 469 | 23 | 0 | 1 | 20 | 0 | 2 | 16 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0005 | 0/0 | 469 | 23 | 12 | 3 | 5 | 0 | 3 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0006 | 0/0 | 469 | 10 | 0 | 2 | 1 | 2 | 5 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0007 | 0/0 | 469 | 9 | 0 | 3 | 2 | 0 | 4 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0008 | 0/0 | 469 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0009 | 0/0 | 469 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0010 | 0/0 | 433 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1410 | 114 | 47 | 9 | 43 | 3 | 12 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0002 | 1/0 | 1410 | 100 | 26 | 22 | 37 | 4 | 10 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0003 | 0/1 | 1410 | 26 | 4 | 6 | 12 | 1 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0004 | 0/0 | 1410 | 23 | 12 | 3 | 5 | 0 | 3 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0005 | 0/0 | 1410 | 22 | 0 | 1 | 19 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0006 | 0/0 | 1410 | 10 | 0 | 2 | 1 | 2 | 5 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0007 | 0/0 | 1410 | 9 | 0 | 3 | 2 | 0 | 4 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0008 | 0/0 | 1410 | 3 | 0 | 3 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0009 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0010 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
c0011 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1023 | 246 | 57 | 40 | 104 | 9 | 35 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0002 | 0/1 | 1023 | 47 | 19 | 10 | 15 | 1 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0003 | 0/0 | 1023 | 7 | 7 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0004 | 0/0 | 1023 | 5 | 5 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0005 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0006 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0007 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0008 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
t0009 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1410 | 114 | 47 | 9 | 43 | 3 | 12 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002c0002 | 1/0 | 1410 | 100 | 26 | 22 | 37 | 4 | 10 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0003c0003 | 0/1 | 1410 | 26 | 4 | 6 | 12 | 1 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0004c0005 | 0/0 | 1410 | 22 | 0 | 1 | 19 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0004c0009 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0005c0004 | 0/0 | 1410 | 23 | 12 | 3 | 5 | 0 | 3 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0006c0006 | 0/0 | 1410 | 10 | 0 | 2 | 1 | 2 | 5 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0007c0007 | 0/0 | 1410 | 9 | 0 | 3 | 2 | 0 | 4 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0008c0008 | 0/0 | 1410 | 3 | 0 | 3 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0009c0010 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0010c0011 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2432 | 104 | 38 | 9 | 43 | 3 | 11 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0001c0001t0002 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0001c0001t0003 | 0/0 | 2432 | 7 | 7 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0001c0001t0005 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0001c0001t0007 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002c0002t0001 | 1/0 | 2432 | 56 | 5 | 16 | 21 | 3 | 10 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002c0002t0002 | 0/0 | 2432 | 38 | 16 | 6 | 15 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002c0002t0004 | 0/0 | 2432 | 5 | 5 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0002c0002t0006 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0003c0003t0001 | 0/0 | 2432 | 22 | 2 | 5 | 12 | 1 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0003c0003t0002 | 0/1 | 2432 | 4 | 2 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0004c0005t0001 | 0/0 | 2432 | 22 | 0 | 1 | 19 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0004c0009t0001 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0005c0004t0001 | 0/0 | 2432 | 21 | 11 | 3 | 5 | 0 | 2 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0005c0004t0008 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0005c0004t0009 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0006c0006t0001 | 0/0 | 2432 | 10 | 0 | 2 | 1 | 2 | 5 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0007c0007t0001 | 0/0 | 2432 | 6 | 0 | 1 | 2 | 0 | 3 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0007c0007t0002 | 0/0 | 2432 | 3 | 0 | 2 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0008c0008t0001 | 0/0 | 2432 | 2 | 0 | 2 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0008c0008t0002 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0009c0010t0001 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
a0010c0011t0001 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | copy fasta | chr6 | 46544580 | 46657818 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0002c0002t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0002g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0003c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0004c0009t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0008g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0005c0004t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0006c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0007c0007t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0008c0008t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0008c0008t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0008c0008t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0009c0010t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
a0010c0011t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0002 | g0180 | EUR | GBR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0281 | EUR | FIN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00408 | hp2 | a0004 | c0005 | t0001 | g0032 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00609 | hp2 | a0007 | c0007 | t0001 | g0037 | EAS | CHS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00738 | hp1 | a0007 | c0007 | t0002 | g0034 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01069 | hp2 | a0005 | c0004 | t0001 | g0285 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01071 | hp1 | a0003 | c0003 | t0001 | g0218 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01074 | hp2 | a0003 | c0003 | t0001 | g0205 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0201 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01175 | hp1 | a0006 | c0006 | t0001 | g0008 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0213 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01243 | hp1 | a0005 | c0004 | t0001 | g0287 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01243 | hp2 | a0008 | c0008 | t0001 | g0027 | AMR | PUR | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01255 | hp2 | a0005 | c0004 | t0001 | g0283 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01256 | hp2 | a0008 | c0008 | t0001 | g0015 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01261 | hp1 | a0006 | c0006 | t0001 | g0004 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01346 | hp2 | a0004 | c0005 | t0001 | g0044 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01433 | hp1 | a0009 | c0010 | t0001 | g0197 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01433 | hp2 | a0007 | c0007 | t0002 | g0033 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01516 | hp1 | a0006 | c0006 | t0001 | g0043 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0212 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0211 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01891 | hp2 | a0003 | c0003 | t0002 | g0257 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01952 | hp2 | a0003 | c0003 | t0001 | g0048 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01975 | hp1 | a0007 | c0007 | t0001 | g0005 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02015 | hp2 | a0004 | c0009 | t0001 | g0028 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02027 | hp1 | a0004 | c0005 | t0001 | g0017 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02027 | hp2 | a0006 | c0006 | t0001 | g0003 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02055 | hp2 | a0002 | c0002 | t0004 | g0307 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02056 | hp1 | a0005 | c0004 | t0001 | g0269 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02083 | hp2 | a0007 | c0007 | t0001 | g0002 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02132 | hp1 | a0004 | c0005 | t0001 | g0024 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02165 | hp1 | a0005 | c0004 | t0001 | g0192 | EAS | CDX | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | CDX | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0274 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02300 | hp2 | a0008 | c0008 | t0002 | g0014 | AMR | PEL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0272 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02451 | hp2 | a0005 | c0004 | t0001 | g0271 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02523 | hp1 | a0005 | c0004 | t0001 | g0278 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | KHV | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02602 | hp1 | a0006 | c0006 | t0001 | g0023 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0199 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02622 | hp2 | a0005 | c0004 | t0001 | g0286 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02630 | hp1 | a0005 | c0004 | t0001 | g0237 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02647 | hp1 | a0005 | c0004 | t0001 | g0288 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02647 | hp2 | a0002 | c0002 | t0004 | g0306 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02683 | hp2 | a0006 | c0006 | t0001 | g0007 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02698 | hp1 | a0005 | c0004 | t0001 | g0282 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02698 | hp2 | a0006 | c0006 | t0001 | g0001 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02723 | hp2 | a0010 | c0011 | t0001 | g0178 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02738 | hp2 | a0006 | c0006 | t0001 | g0006 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02886 | hp2 | a0005 | c0004 | t0001 | g0275 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0256 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0302 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02965 | hp2 | a0005 | c0004 | t0001 | g0276 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02970 | hp2 | a0005 | c0004 | t0009 | g0304 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03017 | hp2 | a0007 | c0007 | t0001 | g0026 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0308 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03098 | hp1 | a0005 | c0004 | t0001 | g0279 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0300 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03195 | hp1 | a0005 | c0004 | t0001 | g0289 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03239 | hp1 | a0004 | c0005 | t0001 | g0013 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0301 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0305 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03654 | hp2 | a0004 | c0005 | t0001 | g0019 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03688 | hp2 | a0007 | c0007 | t0001 | g0011 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0217 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03834 | hp2 | a0007 | c0007 | t0002 | g0035 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03927 | hp1 | a0005 | c0004 | t0001 | g0233 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0105 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04115 | hp1 | a0005 | c0004 | t0008 | g0303 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04199 | hp2 | a0007 | c0007 | t0001 | g0016 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0094 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG04204 | hp2 | a0006 | c0006 | t0001 | g0009 | SAS | STU | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18940 | hp1 | a0004 | c0005 | t0001 | g0038 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18942 | hp2 | a0004 | c0005 | t0001 | g0018 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18951 | hp2 | a0004 | c0005 | t0001 | g0022 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18960 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18968 | hp1 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18975 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18977 | hp2 | a0004 | c0005 | t0001 | g0030 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18982 | hp1 | a0004 | c0005 | t0001 | g0041 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0219 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18994 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18994 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18997 | hp1 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19000 | hp1 | a0004 | c0005 | t0001 | g0020 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19000 | hp2 | a0002 | c0002 | t0006 | g0110 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19002 | hp2 | a0004 | c0005 | t0001 | g0029 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19005 | hp1 | a0004 | c0005 | t0001 | g0040 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19030 | hp2 | a0005 | c0004 | t0001 | g0280 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19058 | hp2 | a0004 | c0005 | t0001 | g0042 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19065 | hp1 | a0004 | c0005 | t0001 | g0031 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19068 | hp1 | a0005 | c0004 | t0001 | g0270 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19070 | hp2 | a0004 | c0005 | t0001 | g0021 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19078 | hp1 | a0004 | c0005 | t0001 | g0025 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19083 | hp2 | a0005 | c0004 | t0001 | g0268 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19086 | hp1 | a0004 | c0005 | t0001 | g0012 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19090 | hp2 | a0004 | c0005 | t0001 | g0039 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | YRI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | ASW | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20129 | hp2 | a0005 | c0004 | t0001 | g0284 | AFR | ASW | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0119 | EUR | TSI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20752 | hp2 | a0006 | c0006 | t0001 | g0001 | EUR | TSI | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | GIH | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0164 | SAS | GIH | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0296 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0133 | AFR | MSL | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA18955 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | USA | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA20300 | hp2 | a0002 | c0002 | t0004 | g0309 | AFR | USA | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
NA21309 | hp2 | a0005 | c0004 | t0001 | g0258 | AFR | LWK | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0002 | g0221 | REF | REF | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0209 | REF | REF | CYP39A1_chr6_46544580_46657818 | CYP39A1 | chr6 | 46544580 | 46657818 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46596080
|
A | T | 5 | a0001a0004a0005others(2): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
missense_variant | MODERATE | c.972T>A | p.Asn324Lys | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/12 | 1208/2432 | 972/1410 | 324/469 | chr6 | 46596080 | ||
chr6:46625487
|
A | G | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.862T>C | p.Tyr288His | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/12 | 1098/2432 | 862/1410 | 288/469 | chr6 | 46625487 | ||
chr6:46629865
|
ACTGTTGG others(1424): Show |
A | 1 | a0010 | 1 | HG02723.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.733-226_840+1097de others(1): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/12 | chr6 | 46629865 | ||||||
chr6:46642168
|
C | T | 4 | a0003a0004a0005others(1): Show | 81 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(78): Show |
missense_variant | MODERATE | c.308G>A | p.Arg103His | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/12 | 544/2432 | 308/1410 | 103/469 | chr6 | 46642168 | ||
chr6:46652515
|
C | G | 4 | a0004a0006a0007others(1): Show | 45 | HG00408.hp2 HG00609.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.68G>C | p.Arg23Pro | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 304/2432 | 68/1410 | 23/469 | chr6 | 46652515 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46631035
|
C | T | 1 | a0004c0009 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.768G>A | p.Thr256Thr | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/12 | 1004/2432 | 768/1410 | 256/469 | chr6 | 46631035 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46549729
|
A | G | 1 | a0001c0001t0005 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 637 | chr6 | 46549729 | |||||
chr6:46550005
|
C | T | 6 | a0001c0001t0002a0002c0002t0002a0002c0002t0004others(3): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*361G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 361 | chr6 | 46550005 | |||||
chr6:46550010
|
A | G | 1 | a0001c0001t0003 | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*356T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 356 | chr6 | 46550010 | |||||
chr6:46550228
|
C | A | 1 | a0002c0002t0006 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 138 | chr6 | 46550228 | |||||
chr6:46550341
|
T | C | 1 | a0001c0001t0007 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 12/12 | 25 | chr6 | 46550341 | |||||
chr6:46652588
|
T | C | 1 | a0005c0004t0008 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 6 | chr6 | 46652588 | |||||
chr6:46652664
|
C | A | 1 | a0005c0004t0009 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 82 | chr6 | 46652664 | |||||
chr6:46652700
|
G | C | 1 | a0002c0002t0004 | 5 | HG02055.hp2 HG02647.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-118C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/12 | 118 | chr6 | 46652700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46550450
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1339-13T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550450 | ||||||
chr6:46550670
|
C | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1339-233G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550670 | ||||||
chr6:46550725
|
C | G | 1 | a0002c0002t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1339-288G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550725 | ||||||
chr6:46550896
|
T | A | 3 | a0002c0002t0001g0267a0003c0003t0001g0200a0008c0008t0001g0027 | 3 | HG01109.hp1 HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1339-459A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550896 | ||||||
chr6:46550925
|
C | G | 1 | a0002c0002t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1339-488G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550925 | ||||||
chr6:46550956
|
A | G | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1339-519T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550956 | ||||||
chr6:46550970
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-533G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46550970 | ||||||
chr6:46551001
|
G | A | 1 | a0002c0002t0001g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1339-564C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551001 | ||||||
chr6:46551283
|
GTA | G | 45 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(42): Show | 45 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.1339-848_1339-847d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551283 | ||||||
chr6:46551284
|
T | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1339-847A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551284 | ||||||
chr6:46551369
|
G | GAA | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1339-934_1339-933d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551369 | ||||||
chr6:46551369
|
GA | G | 7 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-933delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551369 | ||||||
chr6:46551459
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1339-1022A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551459 | ||||||
chr6:46551473
|
C | T | 31 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(28): Show | 31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1339-1036G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551473 | ||||||
chr6:46551489
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1339-1052A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551489 | ||||||
chr6:46551748
|
C | T | 31 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(28): Show | 31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1339-1311G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551748 | ||||||
chr6:46551812
|
T | A | 1 | a0005c0004t0001g0258 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-1375A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46551812 | ||||||
chr6:46552004
|
T | C | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1339-1567A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552004 | ||||||
chr6:46552128
|
A | G | 2 | a0003c0003t0001g0199a0007c0007t0001g0011 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1338+1639T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552128 | ||||||
chr6:46552434
|
A | G | 1 | a0004c0005t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1338+1333T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552434 | ||||||
chr6:46552519
|
T | C | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1338+1248A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552519 | ||||||
chr6:46552980
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1338+787C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46552980 | ||||||
chr6:46553066
|
C | T | 1 | a0001c0001t0003g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+701G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553066 | ||||||
chr6:46553073
|
C | CA | 8 | a0002c0002t0002g0108a0002c0002t0002g0150a0002c0002t0002g0151others(5): Show | 8 | HG01071.hp1 HG02015.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+693dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553073 | ||||||
chr6:46553073
|
CA | C | 83 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1338+693delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553073 | ||||||
chr6:46553093
|
A | C | 3 | a0001c0001t0001g0231a0002c0002t0001g0194a0002c0002t0001g0198 | 3 | NA18972.hp1 NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1338+674T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553093 | ||||||
chr6:46553096
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+671C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553096 | ||||||
chr6:46553123
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+644G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553123 | ||||||
chr6:46553185
|
C | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1338+582G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553185 | ||||||
chr6:46553218
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+549T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553218 | ||||||
chr6:46553309
|
T | A | 1 | a0002c0002t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1338+458A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553309 | ||||||
chr6:46553446
|
T | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1338+321A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553446 | ||||||
chr6:46553512
|
A | T | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+255T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553512 | ||||||
chr6:46553602
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1338+165C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553602 | ||||||
chr6:46553639
|
C | A | 1 | a0002c0002t0002g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1338+128G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553639 | ||||||
chr6:46553699
|
G | A | 1 | a0002c0002t0002g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1338+68C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553699 | ||||||
chr6:46553733
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+34A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 11/11 | chr6 | 46553733 | ||||||
chr6:46553865
|
C | A | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-11G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46553865 | ||||||
chr6:46553983
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-129A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46553983 | ||||||
chr6:46554240
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1251-386A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554240 | ||||||
chr6:46554317
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-463A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554317 | ||||||
chr6:46554369
|
C | A | 3 | a0001c0001t0001g0235a0004c0005t0001g0017a0005c0004t0001g0192 | 3 | HG02027.hp1 HG02165.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1251-515G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554369 | ||||||
chr6:46554442
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-588A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554442 | ||||||
chr6:46554493
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0260a0001c0001t0001g0262others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-639G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554493 | ||||||
chr6:46554519
|
G | C | 1 | a0002c0002t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1251-665C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554519 | ||||||
chr6:46554520
|
C | A | 1 | a0002c0002t0002g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1251-666G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554520 | ||||||
chr6:46554595
|
CACAT | C | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-745_1251-742d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554595 | ||||||
chr6:46554654
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1251-800G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554654 | ||||||
chr6:46554655
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-801G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554655 | ||||||
chr6:46554801
|
A | T | 1 | a0002c0002t0002g0108 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1251-947T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554801 | ||||||
chr6:46554814
|
T | C | 2 | a0004c0005t0001g0021a0004c0005t0001g0022 | 2 | NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1251-960A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554814 | ||||||
chr6:46554817
|
A | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-963T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554817 | ||||||
chr6:46554840
|
A | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-986T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46554840 | ||||||
chr6:46555050
|
G | GAC | 6 | a0001c0001t0001g0096a0002c0002t0001g0173a0002c0002t0002g0111others(3): Show | 6 | HG02027.hp2 HG02109.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-1198_1251-119 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | ||||||
chr6:46555050
|
G | GACAC | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-1200_1251-119 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | ||||||
chr6:46555050
|
GAC | G | 88 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(85): Show | 89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1251-1198_1251-119 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555050 | ||||||
chr6:46555141
|
C | T | 6 | a0002c0002t0001g0051a0002c0002t0001g0107a0002c0002t0001g0112others(3): Show | 6 | HG00558.hp2 HG00597.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-1287G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555141 | ||||||
chr6:46555177
|
T | C | 1 | a0002c0002t0002g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1251-1323A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555177 | ||||||
chr6:46555191
|
C | T | 1 | a0002c0002t0001g0154 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1251-1337G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555191 | ||||||
chr6:46555220
|
T | C | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-1366A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555220 | ||||||
chr6:46555260
|
A | G | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-1406T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555260 | ||||||
chr6:46555423
|
C | A | 2 | a0001c0001t0003g0188a0001c0001t0003g0190 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1251-1569G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555423 | ||||||
chr6:46555559
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-1705A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555559 | ||||||
chr6:46555573
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1251-1719T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555573 | ||||||
chr6:46555845
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1251-1991G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46555845 | ||||||
chr6:46556142
|
T | G | 1 | a0001c0001t0001g0261 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1251-2288A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556142 | ||||||
chr6:46556237
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-2383C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556237 | ||||||
chr6:46556372
|
T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-2518A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556372 | ||||||
chr6:46556408
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-2554T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556408 | ||||||
chr6:46556610
|
C | A | 2 | a0002c0002t0001g0147a0004c0005t0001g0013 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1251-2756G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556610 | ||||||
chr6:46556665
|
G | T | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-2811C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556665 | ||||||
chr6:46556793
|
A | G | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-2939T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556793 | ||||||
chr6:46556803
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1251-2949G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556803 | ||||||
chr6:46556862
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0223 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1251-3008G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46556862 | ||||||
chr6:46557071
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1251-3217T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557071 | ||||||
chr6:46557245
|
C | G | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-3391G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557245 | ||||||
chr6:46557470
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-3616C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557470 | ||||||
chr6:46557603
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-3749T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557603 | ||||||
chr6:46557643
|
T | TA | 52 | a0001c0001t0001g0078a0001c0001t0002g0238a0002c0002t0002g0046others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-3790dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557643 | ||||||
chr6:46557643
|
T | TAA | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-3791_1251-379 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557643 | ||||||
chr6:46557705
|
G | A | 2 | a0002c0002t0001g0080a0002c0002t0001g0084 | 2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1251-3851C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557705 | ||||||
chr6:46557783
|
AAAAATTA others(8): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-3944_1251-393 others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557783 | ||||||
chr6:46557830
|
C | T | 4 | a0001c0001t0003g0075a0001c0001t0003g0188a0001c0001t0003g0189others(1): Show | 4 | HG02572.hp2 HG03540.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-3976G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557830 | ||||||
chr6:46557933
|
C | CA | 82 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(79): Show | 83 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1251-4080dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | ||||||
chr6:46557933
|
C | CAA | 9 | a0001c0001t0001g0293a0001c0001t0003g0075a0001c0001t0003g0186others(6): Show | 9 | HG00741.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-4081_1251-408 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | ||||||
chr6:46557933
|
CA | C | 12 | a0001c0001t0001g0121a0001c0001t0001g0292a0002c0002t0001g0074others(9): Show | 12 | HG01884.hp1 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-4080delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557933 | ||||||
chr6:46557959
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-4105T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46557959 | ||||||
chr6:46558076
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1251-4222G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558076 | ||||||
chr6:46558241
|
G | A | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1251-4387C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558241 | ||||||
chr6:46558398
|
C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-4544G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558398 | ||||||
chr6:46558402
|
C | G | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-4548G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558402 | ||||||
chr6:46558433
|
A | T | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-4579T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558433 | ||||||
chr6:46558518
|
C | T | 1 | a0004c0005t0001g0024 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1251-4664G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558518 | ||||||
chr6:46558544
|
A | C | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1251-4690T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558544 | ||||||
chr6:46558545
|
T | A | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1251-4691A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558545 | ||||||
chr6:46558551
|
A | G | 1 | a0002c0002t0002g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1251-4697T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558551 | ||||||
chr6:46558691
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-4837A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558691 | ||||||
chr6:46558694
|
A | C | 1 | a0005c0004t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1251-4840T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558694 | ||||||
chr6:46558700
|
A | G | 1 | a0005c0004t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1251-4846T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558700 | ||||||
chr6:46558701
|
A | G | 45 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(42): Show | 46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1251-4847T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558701 | ||||||
chr6:46558725
|
C | T | 1 | a0005c0004t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251-4871G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558725 | ||||||
chr6:46558804
|
T | C | 1 | a0005c0004t0001g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1251-4950A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558804 | ||||||
chr6:46558866
|
C | T | 1 | a0005c0004t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1251-5012G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558866 | ||||||
chr6:46558945
|
G | A | 7 | a0002c0002t0002g0133a0002c0002t0002g0191a0002c0002t0002g0236others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-5091C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558945 | ||||||
chr6:46558994
|
C | CA | 22 | a0001c0001t0001g0057a0001c0001t0001g0125a0001c0001t0001g0179others(19): Show | 22 | HG00735.hp1 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1251-5141dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558994 | ||||||
chr6:46558994
|
CA | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG00408.hp2 HG00741.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-5141delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46558994 | ||||||
chr6:46559033
|
T | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-5179A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559033 | ||||||
chr6:46559063
|
G | A | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-5209C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559063 | ||||||
chr6:46559103
|
GAATT | G | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-5253_1251-525 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559103 | ||||||
chr6:46559116
|
G | A | 1 | a0003c0003t0001g0048 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1251-5262C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559116 | ||||||
chr6:46559279
|
A | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-5425T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559279 | ||||||
chr6:46559354
|
A | C | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251-5500T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559354 | ||||||
chr6:46559604
|
C | T | 2 | a0002c0002t0001g0051a0002c0002t0001g0112 | 2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1251-5750G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559604 | ||||||
chr6:46559623
|
G | A | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-5769C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559623 | ||||||
chr6:46559673
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-5819G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559673 | ||||||
chr6:46559890
|
T | C | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-6036A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559890 | ||||||
chr6:46559967
|
A | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-6113T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46559967 | ||||||
chr6:46560374
|
A | AC | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-6521_1251-652 others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560374 | ||||||
chr6:46560560
|
T | A | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251-6706A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560560 | ||||||
chr6:46560614
|
A | G | 1 | a0002c0002t0001g0160 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1251-6760T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560614 | ||||||
chr6:46560778
|
T | TA | 180 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1251-6925dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560778 | ||||||
chr6:46560791
|
C | T | 7 | a0004c0005t0001g0012a0004c0005t0001g0030a0004c0005t0001g0036others(4): Show | 7 | NA18940.hp1 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-6937G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560791 | ||||||
chr6:46560807
|
G | A | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-6953C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560807 | ||||||
chr6:46560847
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-6993C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46560847 | ||||||
chr6:46561076
|
A | C | 1 | a0003c0003t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1251-7222T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561076 | ||||||
chr6:46561139
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7285A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561139 | ||||||
chr6:46561272
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7418A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561272 | ||||||
chr6:46561393
|
G | A | 2 | a0002c0002t0001g0210a0008c0008t0001g0015 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1251-7539C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561393 | ||||||
chr6:46561436
|
G | A | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-7582C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561436 | ||||||
chr6:46561459
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-7605G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561459 | ||||||
chr6:46561635
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1251-7781G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561635 | ||||||
chr6:46561684
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-7830C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561684 | ||||||
chr6:46561702
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1251-7848C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561702 | ||||||
chr6:46561867
|
G | C | 6 | a0002c0002t0001g0155a0002c0002t0001g0161a0002c0002t0001g0181others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-8013C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46561867 | ||||||
chr6:46562126
|
G | GA | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-8273dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562126 | ||||||
chr6:46562183
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-8329A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562183 | ||||||
chr6:46562283
|
A | G | 44 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-8429T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562283 | ||||||
chr6:46562353
|
C | CA | 9 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(6): Show | 9 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-8500dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562353 | ||||||
chr6:46562377
|
T | G | 1 | a0003c0003t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1251-8523A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562377 | ||||||
chr6:46562625
|
C | T | 3 | a0003c0003t0001g0201a0003c0003t0001g0205a0003c0003t0001g0218 | 3 | HG01071.hp1 HG01074.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1251-8771G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562625 | ||||||
chr6:46562695
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1251-8841C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562695 | ||||||
chr6:46562754
|
C | T | 5 | a0002c0002t0002g0114a0002c0002t0004g0306a0002c0002t0004g0307others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-8900G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562754 | ||||||
chr6:46562867
|
T | C | 1 | a0005c0004t0001g0269 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1251-9013A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562867 | ||||||
chr6:46562963
|
T | G | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1251-9109A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46562963 | ||||||
chr6:46563113
|
G | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-9259C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563113 | ||||||
chr6:46563115
|
C | CA | 23 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0290others(20): Show | 23 | HG00741.hp1 HG01069.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-9262dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | ||||||
chr6:46563115
|
C | CAA | 40 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(37): Show | 41 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1251-9263_1251-926 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | ||||||
chr6:46563115
|
CA | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0225a0001c0001t0002g0238others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-9262delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563115 | ||||||
chr6:46563201
|
T | C | 1 | a0003c0003t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1251-9347A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563201 | ||||||
chr6:46563243
|
G | C | 1 | a0007c0007t0001g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1251-9389C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563243 | ||||||
chr6:46563257
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-9403G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563257 | ||||||
chr6:46563439
|
A | G | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-9585T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563439 | ||||||
chr6:46563598
|
T | G | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1251-9744A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563598 | ||||||
chr6:46563748
|
G | C | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-9894C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563748 | ||||||
chr6:46563750
|
G | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-9896C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563750 | ||||||
chr6:46563911
|
T | C | 180 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1251-10057A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46563911 | ||||||
chr6:46564087
|
GTTTTTTA others(11): Show |
G | 12 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10251_1251-10 others(24): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564087 | ||||||
chr6:46564087
|
GTTTTTTA others(26): Show |
G | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10266_1251-10 others(39): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564087 | ||||||
chr6:46564088
|
TTTTTTAT others(6): Show |
T | 30 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10247_1251-10 others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564088 | ||||||
chr6:46564089
|
T | A | 32 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0055others(29): Show | 32 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1251-10235A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564089 | ||||||
chr6:46564090
|
TTTTATTT others(21): Show |
T | 4 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0290others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10264_1251-10 others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | ||||||
chr6:46564090
|
TTTTATTT others(31): Show |
T | 26 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(23): Show | 26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10274_1251-10 others(44): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | ||||||
chr6:46564090
|
TTTTATTT others(41): Show |
T | 2 | a0001c0001t0003g0187a0001c0001t0005g0273 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-10284_1251-10 others(54): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564090 | ||||||
chr6:46564096
|
T | TTTATTTT others(248): Show |
1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-10243_1251-10 others(261): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564096 | ||||||
chr6:46564099
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-10245C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564099 | ||||||
chr6:46564102
|
T | A | 30 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10248A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564102 | ||||||
chr6:46564105
|
T | A | 30 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10251A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564105 | ||||||
chr6:46564107
|
T | A | 12 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10253A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564107 | ||||||
chr6:46564108
|
TTATTTTA others(3): Show |
T | 1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-10264_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564108 | ||||||
chr6:46564117
|
TCTA | T | 30 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10266_1251-10 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564117 | ||||||
chr6:46564118
|
C | T | 13 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0064others(10): Show | 13 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1251-10264G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564118 | ||||||
chr6:46564120
|
ATT | A | 12 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10268_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564120 | ||||||
chr6:46564121
|
T | A | 30 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 31 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-10267A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564121 | ||||||
chr6:46564122
|
T | A | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10268A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564122 | ||||||
chr6:46564127
|
TC | T | 12 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG00741.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-10274delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564127 | ||||||
chr6:46564128
|
C | T | 44 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-10274G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564128 | ||||||
chr6:46564130
|
ATT | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0290others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10278_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564130 | ||||||
chr6:46564136
|
TTC | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10284_1251-10 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564136 | ||||||
chr6:46564137
|
TC | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0290others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10284delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564137 | ||||||
chr6:46564138
|
C | CTATTCTA others(3): Show |
1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1251-10294_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | ||||||
chr6:46564138
|
C | T | 69 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(66): Show | 70 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1251-10284G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | ||||||
chr6:46564138
|
CTATTCTA others(3): Show |
C | 14 | a0001c0001t0002g0238a0002c0002t0001g0067a0002c0002t0001g0109others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1251-10294_1251-10 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564138 | ||||||
chr6:46564142
|
TC | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10289delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564142 | ||||||
chr6:46564142
|
TCTA | T | 26 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(23): Show | 26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10291_1251-10 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564142 | ||||||
chr6:46564143
|
C | T | 49 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(46): Show | 50 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1251-10289G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564143 | ||||||
chr6:46564146
|
T | A | 26 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(23): Show | 26 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1251-10292A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564146 | ||||||
chr6:46564153
|
C | T | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564153 | ||||||
chr6:46564163
|
C | T | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10309G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564163 | ||||||
chr6:46564173
|
C | T | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10319G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564173 | ||||||
chr6:46564180
|
ATTCTAT | A | 30 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0053others(27): Show | 30 | HG00735.hp2 HG00741.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1251-10332_1251-10 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564180 | ||||||
chr6:46564183
|
C | T | 54 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0055others(51): Show | 55 | HG00597.hp2 HG00639.hp1 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.1251-10329G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564183 | ||||||
chr6:46564185
|
AT | A | 52 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0055others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1251-10332delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564185 | ||||||
chr6:46564210
|
A | G | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-10356T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564210 | ||||||
chr6:46564223
|
C | G | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10369G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564223 | ||||||
chr6:46564260
|
C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-10406G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564260 | ||||||
chr6:46564367
|
T | C | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10513A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564367 | ||||||
chr6:46564377
|
G | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-10523C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564377 | ||||||
chr6:46564398
|
A | G | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-10544T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564398 | ||||||
chr6:46564577
|
C | A | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1251-10723G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564577 | ||||||
chr6:46564727
|
C | T | 9 | a0001c0001t0002g0238a0002c0002t0002g0100a0002c0002t0002g0102others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-10873G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46564727 | ||||||
chr6:46565078
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-11224G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565078 | ||||||
chr6:46565087
|
C | CA | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-11234dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565087 | ||||||
chr6:46565205
|
G | A | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1251-11351C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565205 | ||||||
chr6:46565259
|
C | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-11405G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565259 | ||||||
chr6:46565343
|
C | A | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-11489G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565343 | ||||||
chr6:46565356
|
A | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-11502T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565356 | ||||||
chr6:46565417
|
A | G | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1251-11563T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565417 | ||||||
chr6:46565507
|
GAAATAAA others(2): Show |
G | 82 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(79): Show | 83 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.1251-11662_1251-11 others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565507 | ||||||
chr6:46565511
|
TAAATAAA others(3): Show |
T | 1 | a0004c0005t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1251-11667_1251-11 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565511 | ||||||
chr6:46565693
|
C | G | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1251-11839G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565693 | ||||||
chr6:46565709
|
G | A | 1 | a0005c0004t0001g0270 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1251-11855C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565709 | ||||||
chr6:46565805
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1251-11951C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565805 | ||||||
chr6:46565971
|
G | T | 1 | a0005c0004t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1251-12117C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565971 | ||||||
chr6:46565988
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-12134G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46565988 | ||||||
chr6:46566003
|
T | G | 1 | a0002c0002t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1251-12149A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566003 | ||||||
chr6:46566035
|
C | G | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-12181G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566035 | ||||||
chr6:46566166
|
C | A | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-12312G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566166 | ||||||
chr6:46566182
|
G | C | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-12328C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566182 | ||||||
chr6:46566248
|
T | C | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1251-12394A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566248 | ||||||
chr6:46566530
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1251-12676C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566530 | ||||||
chr6:46566561
|
C | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-12707G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566561 | ||||||
chr6:46566739
|
T | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-12885A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566739 | ||||||
chr6:46566742
|
C | T | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-12888G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566742 | ||||||
chr6:46566767
|
A | G | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-12913T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566767 | ||||||
chr6:46566834
|
TTA | T | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-12982_1251-12 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566834 | ||||||
chr6:46566836
|
A | T | 1 | a0002c0002t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1251-12982T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566836 | ||||||
chr6:46566843
|
T | A | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1251-12989A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566843 | ||||||
chr6:46566874
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-13020T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566874 | ||||||
chr6:46566889
|
C | T | 1 | a0002c0002t0001g0174 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1251-13035G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46566889 | ||||||
chr6:46567035
|
A | G | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1251-13181T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567035 | ||||||
chr6:46567134
|
A | G | 1 | a0002c0002t0001g0135 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1251-13280T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567134 | ||||||
chr6:46567262
|
T | C | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1251-13408A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567262 | ||||||
chr6:46567340
|
A | ATG | 84 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(81): Show | 85 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1251-13487_1251-13 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567340 | ||||||
chr6:46567606
|
T | C | 1 | a0002c0002t0001g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1251-13752A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567606 | ||||||
chr6:46567740
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-13886G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567740 | ||||||
chr6:46567994
|
TTTA | T | 39 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(36): Show | 40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1251-14143_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567994 | ||||||
chr6:46567995
|
TTAA | T | 90 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(87): Show | 90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1251-14144_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567995 | ||||||
chr6:46567996
|
T | A | 3 | a0005c0004t0001g0275a0005c0004t0001g0280a0007c0007t0001g0011 | 3 | HG02886.hp2 HG03688.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1251-14142A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | ||||||
chr6:46567996
|
TA | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1251-14143delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | ||||||
chr6:46567996
|
TAAA | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG01255.hp2 HG02572.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-14145_1251-14 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567996 | ||||||
chr6:46567997
|
A | T | 3 | a0002c0002t0001g0164a0002c0002t0001g0165a0004c0005t0001g0030 | 3 | HG02683.hp1 NA18977.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1251-14143T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567997 | ||||||
chr6:46567998
|
A | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0225 | 3 | HG02976.hp1 HG03139.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1251-14144T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46567998 | ||||||
chr6:46568126
|
G | C | 3 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221 | 3 | HG00735.hp1 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1251-14272C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568126 | ||||||
chr6:46568157
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1251-14303A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568157 | ||||||
chr6:46568215
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1251-14361A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568215 | ||||||
chr6:46568250
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1251-14396C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568250 | ||||||
chr6:46568500
|
CT | C | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-14647delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568500 | ||||||
chr6:46568678
|
G | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1251-14824C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568678 | ||||||
chr6:46568918
|
G | T | 7 | a0001c0001t0001g0072a0001c0001t0001g0083a0002c0002t0001g0113others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-15064C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568918 | ||||||
chr6:46568920
|
C | CA | 93 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(90): Show | 94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1251-15067dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568920 | ||||||
chr6:46568920
|
C | CAA | 37 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(34): Show | 37 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.1251-15068_1251-15 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46568920 | ||||||
chr6:46569229
|
T | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-15375A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569229 | ||||||
chr6:46569266
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-15412T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569266 | ||||||
chr6:46569382
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-15528C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569382 | ||||||
chr6:46569477
|
A | T | 7 | a0004c0005t0001g0012a0004c0005t0001g0030a0004c0005t0001g0036others(4): Show | 7 | NA18940.hp1 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-15623T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569477 | ||||||
chr6:46569698
|
C | G | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-15844G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569698 | ||||||
chr6:46569803
|
T | C | 5 | a0002c0002t0001g0113a0002c0002t0001g0169a0002c0002t0001g0170others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-15949A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569803 | ||||||
chr6:46569819
|
G | A | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251-15965C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569819 | ||||||
chr6:46569891
|
T | C | 1 | a0002c0002t0006g0110 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1251-16037A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569891 | ||||||
chr6:46569925
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16071C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46569925 | ||||||
chr6:46570110
|
C | G | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1251-16256G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570110 | ||||||
chr6:46570174
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16320A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570174 | ||||||
chr6:46570175
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16321C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570175 | ||||||
chr6:46570264
|
T | A | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-16410A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570264 | ||||||
chr6:46570395
|
C | T | 2 | a0003c0003t0001g0216a0003c0003t0001g0222 | 2 | NA18960.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1251-16541G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570395 | ||||||
chr6:46570424
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1251-16570A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570424 | ||||||
chr6:46570666
|
G | A | 1 | a0001c0001t0003g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1250+16411C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570666 | ||||||
chr6:46570737
|
T | G | 1 | a0002c0002t0001g0130 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1250+16340A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570737 | ||||||
chr6:46570824
|
C | T | 3 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221 | 3 | HG00735.hp1 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1250+16253G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570824 | ||||||
chr6:46570907
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+16170G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570907 | ||||||
chr6:46570914
|
A | G | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+16163T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46570914 | ||||||
chr6:46571034
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+16043G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571034 | ||||||
chr6:46571045
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+16032G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571045 | ||||||
chr6:46571099
|
C | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+15978G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571099 | ||||||
chr6:46571176
|
T | C | 2 | a0002c0002t0002g0300a0002c0002t0002g0301 | 2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1250+15901A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571176 | ||||||
chr6:46571271
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+15806A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571271 | ||||||
chr6:46571515
|
C | A | 4 | a0001c0001t0001g0244a0001c0001t0001g0260a0001c0001t0001g0262others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+15562G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571515 | ||||||
chr6:46571539
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+15538A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571539 | ||||||
chr6:46571558
|
CATTT | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15515_1250+15 others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571558 | ||||||
chr6:46571662
|
C | CT | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15414dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571662 | ||||||
chr6:46571675
|
C | T | 7 | a0002c0002t0001g0074a0002c0002t0001g0080a0002c0002t0001g0084others(4): Show | 7 | HG00423.hp2 HG01258.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+15402G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571675 | ||||||
chr6:46571723
|
C | T | 1 | a0003c0003t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1250+15354G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571723 | ||||||
chr6:46571998
|
T | C | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+15079A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46571998 | ||||||
chr6:46572070
|
T | A | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+15007A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572070 | ||||||
chr6:46572094
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+14983T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572094 | ||||||
chr6:46572115
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14962A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572115 | ||||||
chr6:46572187
|
TA | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+14889delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572187 | ||||||
chr6:46572241
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1250+14836T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572241 | ||||||
chr6:46572274
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14803A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572274 | ||||||
chr6:46572297
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1250+14780A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572297 | ||||||
chr6:46572717
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+14360C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572717 | ||||||
chr6:46572944
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+14133A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46572944 | ||||||
chr6:46573081
|
G | A | 1 | a0002c0002t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1250+13996C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573081 | ||||||
chr6:46573149
|
A | T | 1 | a0004c0005t0001g0018 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1250+13928T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573149 | ||||||
chr6:46573171
|
G | A | 31 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(28): Show | 31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+13906C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573171 | ||||||
chr6:46573339
|
G | C | 1 | a0004c0005t0001g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1250+13738C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573339 | ||||||
chr6:46573364
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+13713A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573364 | ||||||
chr6:46573494
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+13583C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573494 | ||||||
chr6:46573524
|
G | T | 301 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(298): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1250+13553C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573524 | ||||||
chr6:46573725
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+13352A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46573725 | ||||||
chr6:46574353
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1250+12724G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574353 | ||||||
chr6:46574489
|
G | A | 31 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(28): Show | 31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+12588C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574489 | ||||||
chr6:46574581
|
T | C | 16 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+12496A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574581 | ||||||
chr6:46574830
|
A | G | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+12247T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574830 | ||||||
chr6:46574878
|
C | T | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+12199G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574878 | ||||||
chr6:46574987
|
C | T | 2 | a0001c0001t0001g0096a0010c0011t0001g0178 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1250+12090G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46574987 | ||||||
chr6:46575010
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0245 | 2 | NA18985.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1250+12067A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575010 | ||||||
chr6:46575020
|
T | C | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1250+12057A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575020 | ||||||
chr6:46575067
|
T | C | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 45 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1250+12010A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575067 | ||||||
chr6:46575096
|
T | G | 25 | a0001c0001t0001g0091a0001c0001t0001g0131a0001c0001t0001g0132others(22): Show | 25 | HG02015.hp2 HG02027.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.1250+11981A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575096 | ||||||
chr6:46575151
|
C | T | 31 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(28): Show | 31 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1250+11926G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575151 | ||||||
chr6:46575460
|
A | T | 1 | a0002c0002t0001g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1250+11617T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575460 | ||||||
chr6:46575596
|
CT | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+11480delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575596 | ||||||
chr6:46575725
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+11352G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575725 | ||||||
chr6:46575746
|
C | T | 1 | a0004c0005t0001g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1250+11331G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575746 | ||||||
chr6:46575946
|
T | A | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1250+11131A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46575946 | ||||||
chr6:46576098
|
G | A | 7 | a0001c0001t0001g0072a0001c0001t0001g0083a0002c0002t0001g0113others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250+10979C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576098 | ||||||
chr6:46576261
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+10816G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576261 | ||||||
chr6:46576397
|
G | A | 1 | a0004c0005t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1250+10680C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576397 | ||||||
chr6:46576522
|
T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+10555A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46576522 | ||||||
chr6:46577312
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1250+9765G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577312 | ||||||
chr6:46577335
|
C | T | 2 | a0002c0002t0001g0210a0008c0008t0001g0015 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+9742G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577335 | ||||||
chr6:46577575
|
T | C | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1250+9502A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577575 | ||||||
chr6:46577620
|
G | A | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1250+9457C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577620 | ||||||
chr6:46577631
|
T | G | 1 | a0004c0005t0001g0032 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1250+9446A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577631 | ||||||
chr6:46577674
|
G | A | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250+9403C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577674 | ||||||
chr6:46577775
|
TA | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+9301delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577775 | ||||||
chr6:46577828
|
G | A | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+9249C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577828 | ||||||
chr6:46577855
|
G | A | 1 | a0002c0002t0001g0298 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1250+9222C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46577855 | ||||||
chr6:46578008
|
G | A | 1 | a0003c0003t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1250+9069C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578008 | ||||||
chr6:46578157
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+8920A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578157 | ||||||
chr6:46578173
|
T | C | 1 | a0002c0002t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1250+8904A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578173 | ||||||
chr6:46578298
|
C | A | 24 | a0001c0001t0001g0091a0001c0001t0001g0131a0001c0001t0001g0132others(21): Show | 24 | HG02015.hp2 HG02027.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.1250+8779G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578298 | ||||||
chr6:46578384
|
C | T | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+8693G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578384 | ||||||
chr6:46578653
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1250+8424T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578653 | ||||||
chr6:46578756
|
C | A | 1 | a0002c0002t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1250+8321G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46578756 | ||||||
chr6:46579109
|
C | A | 76 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(73): Show | 77 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1250+7968G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579109 | ||||||
chr6:46579293
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+7784G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579293 | ||||||
chr6:46579444
|
G | A | 1 | a0002c0002t0002g0151 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1250+7633C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579444 | ||||||
chr6:46579584
|
C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0128 | 2 | HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1250+7493G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579584 | ||||||
chr6:46579765
|
C | A | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+7312G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46579765 | ||||||
chr6:46580312
|
C | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+6765G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580312 | ||||||
chr6:46580337
|
T | C | 135 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(132): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+6740A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580337 | ||||||
chr6:46580495
|
A | C | 76 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(73): Show | 77 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1250+6582T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580495 | ||||||
chr6:46580554
|
C | T | 1 | a0005c0004t0001g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1250+6523G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580554 | ||||||
chr6:46580614
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+6463C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580614 | ||||||
chr6:46580931
|
A | G | 1 | a0005c0004t0008g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1250+6146T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46580931 | ||||||
chr6:46581083
|
C | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0176 | 2 | HG01258.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1250+5994G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581083 | ||||||
chr6:46581095
|
C | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+5982G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581095 | ||||||
chr6:46581192
|
G | C | 2 | a0003c0003t0001g0199a0007c0007t0001g0011 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1250+5885C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581192 | ||||||
chr6:46581199
|
G | A | 26 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0123others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1250+5878C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581199 | ||||||
chr6:46581233
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+5844G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581233 | ||||||
chr6:46581269
|
G | A | 1 | a0002c0002t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1250+5808C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581269 | ||||||
chr6:46581366
|
C | T | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250+5711G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581366 | ||||||
chr6:46581405
|
GA | G | 135 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(132): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+5671delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581405 | ||||||
chr6:46581419
|
A | G | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1250+5658T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581419 | ||||||
chr6:46581767
|
C | T | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250+5310G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581767 | ||||||
chr6:46581768
|
C | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1250+5309G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581768 | ||||||
chr6:46581805
|
C | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+5272G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581805 | ||||||
chr6:46581822
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+5255A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581822 | ||||||
chr6:46581858
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+5219C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581858 | ||||||
chr6:46581986
|
A | G | 4 | a0005c0004t0001g0284a0005c0004t0001g0288a0005c0004t0001g0289others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+5091T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46581986 | ||||||
chr6:46582027
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+5050C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582027 | ||||||
chr6:46582233
|
C | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(133): Show | 137 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1250+4844G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582233 | ||||||
chr6:46582239
|
T | C | 180 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1250+4838A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582239 | ||||||
chr6:46582262
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+4815G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582262 | ||||||
chr6:46582313
|
A | G | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1250+4764T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582313 | ||||||
chr6:46582545
|
C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+4532G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46582545 | ||||||
chr6:46583121
|
T | C | 3 | a0002c0002t0001g0182a0002c0002t0001g0298a0002c0002t0001g0299 | 3 | NA18971.hp1 NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1250+3956A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583121 | ||||||
chr6:46583447
|
A | T | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250+3630T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583447 | ||||||
chr6:46583453
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1250+3624G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583453 | ||||||
chr6:46583600
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+3477C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583600 | ||||||
chr6:46583648
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1250+3429A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583648 | ||||||
chr6:46583779
|
C | T | 2 | a0007c0007t0001g0016a0007c0007t0001g0026 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1250+3298G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583779 | ||||||
chr6:46583892
|
G | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+3185C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46583892 | ||||||
chr6:46584006
|
C | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1250+3071G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584006 | ||||||
chr6:46584121
|
T | G | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+2956A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584121 | ||||||
chr6:46584124
|
G | C | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+2953C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584124 | ||||||
chr6:46584205
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1250+2872C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584205 | ||||||
chr6:46584370
|
C | A | 45 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(42): Show | 46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1250+2707G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584370 | ||||||
chr6:46584463
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+2614G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584463 | ||||||
chr6:46584508
|
C | A | 180 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1250+2569G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584508 | ||||||
chr6:46584582
|
C | T | 6 | a0002c0002t0001g0051a0002c0002t0001g0107a0002c0002t0001g0112others(3): Show | 6 | HG00558.hp2 HG00597.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+2495G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584582 | ||||||
chr6:46584807
|
C | T | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1250+2270G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584807 | ||||||
chr6:46584905
|
A | G | 44 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1250+2172T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584905 | ||||||
chr6:46584935
|
A | G | 1 | a0006c0006t0001g0001 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1250+2142T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584935 | ||||||
chr6:46584966
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+2111C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46584966 | ||||||
chr6:46585322
|
T | TATAG | 95 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0053others(92): Show | 95 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1250+1751_1250+175 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | ||||||
chr6:46585322
|
T | TATAGATA others(1): Show |
4 | a0001c0001t0001g0066a0002c0002t0001g0106a0002c0002t0002g0300others(1): Show | 4 | HG02647.hp1 HG03139.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1747_1250+175 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | ||||||
chr6:46585322
|
TATAG | T | 47 | a0001c0001t0001g0050a0001c0001t0001g0088a0001c0001t0001g0089others(44): Show | 48 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1250+1751_1250+175 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | ||||||
chr6:46585322
|
TATAGATA others(1): Show |
T | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0137others(7): Show | 10 | HG01175.hp1 HG02145.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1250+1747_1250+175 others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | ||||||
chr6:46585322
|
TATAGATA others(5): Show |
T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1743_1250+175 others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585322 | ||||||
chr6:46585360
|
T | C | 3 | a0002c0002t0001g0080a0002c0002t0001g0084a0002c0002t0001g0149 | 3 | HG00423.hp2 NA18951.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1250+1717A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585360 | ||||||
chr6:46585561
|
G | A | 1 | a0002c0002t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1250+1516C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585561 | ||||||
chr6:46585586
|
T | C | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+1491A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585586 | ||||||
chr6:46585711
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+1366G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585711 | ||||||
chr6:46585716
|
A | G | 16 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+1361T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585716 | ||||||
chr6:46585917
|
A | G | 135 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(132): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1250+1160T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585917 | ||||||
chr6:46585933
|
G | A | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1250+1144C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46585933 | ||||||
chr6:46586079
|
G | C | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1250+998C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586079 | ||||||
chr6:46586088
|
T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+989A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586088 | ||||||
chr6:46586126
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+951G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586126 | ||||||
chr6:46586192
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250+885G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586192 | ||||||
chr6:46586331
|
A | T | 39 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(36): Show | 40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+746T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586331 | ||||||
chr6:46586388
|
T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1250+689A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586388 | ||||||
chr6:46586829
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0096 | 3 | HG02109.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1250+248G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 10/11 | chr6 | 46586829 | ||||||
chr6:46587414
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1162-249G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587414 | ||||||
chr6:46587437
|
G | A | 7 | a0001c0001t0001g0072a0001c0001t0001g0083a0002c0002t0001g0113others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162-272C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587437 | ||||||
chr6:46587664
|
G | A | 135 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(132): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1161+370C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587664 | ||||||
chr6:46587711
|
A | G | 1 | a0002c0002t0001g0298 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1161+323T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587711 | ||||||
chr6:46587736
|
C | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG02572.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+298G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46587736 | ||||||
chr6:46588004
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1161+30C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 9/11 | chr6 | 46588004 | ||||||
chr6:46588138
|
G | C | 1 | a0002c0002t0002g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1066-9C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588138 | ||||||
chr6:46588373
|
G | A | 39 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(36): Show | 40 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1066-244C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588373 | ||||||
chr6:46588588
|
T | C | 52 | a0001c0001t0002g0238a0002c0002t0002g0046a0002c0002t0002g0076others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1066-459A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588588 | ||||||
chr6:46588663
|
G | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-534C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588663 | ||||||
chr6:46588696
|
G | A | 3 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221 | 3 | HG00735.hp1 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1066-567C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588696 | ||||||
chr6:46588697
|
G | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066-568C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588697 | ||||||
chr6:46588725
|
G | A | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1066-596C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588725 | ||||||
chr6:46588727
|
C | G | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1066-598G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46588727 | ||||||
chr6:46589073
|
G | A | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1066-944C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589073 | ||||||
chr6:46589282
|
G | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0225 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1066-1153C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589282 | ||||||
chr6:46589346
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1066-1217C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589346 | ||||||
chr6:46589453
|
G | A | 1 | a0002c0002t0002g0143 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1066-1324C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589453 | ||||||
chr6:46589772
|
T | A | 2 | a0001c0001t0001g0292a0005c0004t0001g0286 | 2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1066-1643A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589772 | ||||||
chr6:46589912
|
T | C | 1 | a0002c0002t0001g0154 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1066-1783A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46589912 | ||||||
chr6:46590013
|
T | C | 6 | a0002c0002t0002g0148a0002c0002t0002g0150a0002c0002t0002g0151others(3): Show | 6 | HG02015.hp1 HG02165.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066-1884A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590013 | ||||||
chr6:46590171
|
G | A | 38 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(35): Show | 38 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.1066-2042C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590171 | ||||||
chr6:46590538
|
G | A | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1066-2409C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590538 | ||||||
chr6:46590568
|
T | A | 83 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(80): Show | 84 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.1066-2439A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590568 | ||||||
chr6:46590719
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1066-2590A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590719 | ||||||
chr6:46590974
|
T | C | 7 | a0002c0002t0002g0133a0002c0002t0002g0191a0002c0002t0002g0236others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066-2845A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46590974 | ||||||
chr6:46591041
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1066-2912A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591041 | ||||||
chr6:46591069
|
C | A | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1066-2940G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591069 | ||||||
chr6:46591311
|
C | A | 1 | a0007c0007t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1066-3182G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591311 | ||||||
chr6:46591348
|
T | C | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066-3219A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591348 | ||||||
chr6:46591395
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066-3266T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591395 | ||||||
chr6:46591532
|
T | C | 1 | a0002c0002t0002g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1066-3403A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591532 | ||||||
chr6:46591734
|
A | T | 2 | a0001c0001t0001g0179a0004c0005t0001g0032 | 2 | HG00408.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1066-3605T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591734 | ||||||
chr6:46591936
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1066-3807T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46591936 | ||||||
chr6:46592081
|
T | G | 1 | a0004c0005t0001g0032 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1065+3906A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592081 | ||||||
chr6:46592266
|
A | C | 47 | a0001c0001t0001g0091a0001c0001t0001g0131a0001c0001t0001g0132others(44): Show | 47 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1065+3721T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592266 | ||||||
chr6:46592323
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1065+3664A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592323 | ||||||
chr6:46592323
|
T | C | 1 | a0002c0002t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1065+3664A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592323 | ||||||
chr6:46592661
|
C | T | 1 | a0003c0003t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1065+3326G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592661 | ||||||
chr6:46592679
|
A | G | 170 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1065+3308T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592679 | ||||||
chr6:46592930
|
TGGG | T | 3 | a0001c0001t0001g0134a0004c0005t0001g0029a0006c0006t0001g0003 | 3 | HG02027.hp2 NA18970.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1065+3054_1065+305 others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46592930 | ||||||
chr6:46593013
|
A | G | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1065+2974T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593013 | ||||||
chr6:46593231
|
C | T | 16 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1065+2756G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593231 | ||||||
chr6:46593822
|
C | T | 1 | a0006c0006t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1065+2165G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46593822 | ||||||
chr6:46594150
|
G | A | 1 | a0003c0003t0001g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1065+1837C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594150 | ||||||
chr6:46594403
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1065+1584G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594403 | ||||||
chr6:46594463
|
C | T | 1 | a0004c0005t0001g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1065+1524G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594463 | ||||||
chr6:46594483
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+1504A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594483 | ||||||
chr6:46594554
|
T | C | 7 | a0006c0006t0001g0004a0006c0006t0001g0006a0006c0006t0001g0007others(4): Show | 7 | HG01175.hp1 HG01261.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1065+1433A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594554 | ||||||
chr6:46594651
|
A | G | 8 | a0001c0001t0001g0064a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065+1336T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46594651 | ||||||
chr6:46595032
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1065+955C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595032 | ||||||
chr6:46595205
|
C | T | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+782G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595205 | ||||||
chr6:46595226
|
T | C | 1 | a0004c0005t0001g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1065+761A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595226 | ||||||
chr6:46595440
|
T | C | 2 | a0002c0002t0002g0300a0002c0002t0002g0301 | 2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1065+547A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595440 | ||||||
chr6:46595461
|
T | G | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1065+526A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595461 | ||||||
chr6:46595674
|
A | G | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+313T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595674 | ||||||
chr6:46595981
|
G | C | 1 | a0002c0002t0001g0160 | 1 | HG01258.hp2 | splice_region_variant&intron_variant | LOW | c.1065+6C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 8/11 | chr6 | 46595981 | ||||||
chr6:46596390
|
T | C | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-270A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596390 | ||||||
chr6:46596564
|
C | CT | 13 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(10): Show | 13 | HG00741.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-445dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596564 | ||||||
chr6:46596755
|
C | T | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.932-635G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46596755 | ||||||
chr6:46597063
|
G | T | 1 | a0002c0002t0001g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.932-943C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597063 | ||||||
chr6:46597230
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0292 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.932-1110G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597230 | ||||||
chr6:46597231
|
G | A | 45 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(42): Show | 46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.932-1111C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597231 | ||||||
chr6:46597327
|
C | A | 41 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(38): Show | 42 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.932-1207G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597327 | ||||||
chr6:46597350
|
A | T | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.932-1230T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597350 | ||||||
chr6:46597398
|
A | G | 7 | a0002c0002t0002g0133a0002c0002t0002g0191a0002c0002t0002g0236others(4): Show | 7 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1278T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597398 | ||||||
chr6:46597439
|
C | T | 6 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(3): Show | 6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-1319G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597439 | ||||||
chr6:46597582
|
A | T | 1 | a0006c0006t0001g0001 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.932-1462T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597582 | ||||||
chr6:46597742
|
C | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-1622G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597742 | ||||||
chr6:46597770
|
G | A | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-1650C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597770 | ||||||
chr6:46597831
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.932-1711A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597831 | ||||||
chr6:46597927
|
T | C | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-1807A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46597927 | ||||||
chr6:46598048
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1928G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598048 | ||||||
chr6:46598227
|
T | A | 171 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.932-2107A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598227 | ||||||
chr6:46598330
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.932-2210T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598330 | ||||||
chr6:46598387
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.932-2267T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598387 | ||||||
chr6:46598419
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.932-2299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598419 | ||||||
chr6:46598548
|
C | G | 1 | a0005c0004t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.932-2428G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598548 | ||||||
chr6:46598931
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.932-2811C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46598931 | ||||||
chr6:46599058
|
G | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-2938C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599058 | ||||||
chr6:46599087
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.932-2967C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599087 | ||||||
chr6:46599112
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-2992G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599112 | ||||||
chr6:46599255
|
C | T | 1 | a0007c0007t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.932-3135G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599255 | ||||||
chr6:46599270
|
G | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-3150C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599270 | ||||||
chr6:46599313
|
C | CG | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-3194dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599313 | ||||||
chr6:46599313
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.932-3193G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599313 | ||||||
chr6:46599498
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.932-3378G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599498 | ||||||
chr6:46599556
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0223 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.932-3436G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599556 | ||||||
chr6:46599558
|
C | T | 1 | a0004c0005t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.932-3438G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599558 | ||||||
chr6:46599620
|
C | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-3500G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599620 | ||||||
chr6:46599757
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-3637G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599757 | ||||||
chr6:46599848
|
T | C | 1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.932-3728A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46599848 | ||||||
chr6:46600107
|
CTTTCT | C | 43 | a0001c0001t0001g0131a0001c0001t0001g0132a0002c0002t0001g0130others(40): Show | 43 | HG00609.hp2 HG01243.hp1 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.932-3992_932-3988d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600107 | ||||||
chr6:46600116
|
C | A | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.932-3996G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600116 | ||||||
chr6:46600151
|
T | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4031A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600151 | ||||||
chr6:46600152
|
G | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4032C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600152 | ||||||
chr6:46600160
|
G | C | 1 | a0006c0006t0001g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.932-4040C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600160 | ||||||
chr6:46600325
|
T | C | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-4205A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600325 | ||||||
chr6:46600367
|
C | G | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-4247G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600367 | ||||||
chr6:46600488
|
T | G | 2 | a0002c0002t0001g0156a0002c0002t0001g0157 | 2 | NA18968.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.932-4368A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600488 | ||||||
chr6:46600666
|
G | A | 3 | a0002c0002t0002g0274a0002c0002t0002g0296a0002c0002t0004g0305 | 3 | HG02257.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.932-4546C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600666 | ||||||
chr6:46600850
|
G | A | 1 | a0002c0002t0001g0299 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.932-4730C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600850 | ||||||
chr6:46600921
|
G | C | 1 | a0002c0002t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-4801C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46600921 | ||||||
chr6:46601207
|
GT | G | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-5088delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601207 | ||||||
chr6:46601281
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0083 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-5161C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601281 | ||||||
chr6:46601308
|
G | T | 2 | a0002c0002t0001g0156a0002c0002t0001g0157 | 2 | NA18968.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.932-5188C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601308 | ||||||
chr6:46601353
|
C | A | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-5233G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601353 | ||||||
chr6:46601628
|
A | C | 2 | a0003c0003t0001g0193a0003c0003t0001g0195 | 2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.932-5508T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601628 | ||||||
chr6:46601665
|
C | CTAT | 62 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(59): Show | 62 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.932-5548_932-5546d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | ||||||
chr6:46601665
|
C | CTATTAT | 10 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0099others(7): Show | 11 | HG02258.hp1 HG02602.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.932-5551_932-5546d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | ||||||
chr6:46601665
|
C | CTATTATT others(5): Show |
1 | a0004c0005t0001g0024 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.932-5557_932-5546d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | ||||||
chr6:46601665
|
CTAT | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0177a0001c0001t0001g0261others(4): Show | 7 | HG00738.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-5548_932-5546d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | ||||||
chr6:46601665
|
CTATTAT | C | 34 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(31): Show | 34 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.932-5551_932-5546d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601665 | ||||||
chr6:46601688
|
A | G | 2 | a0002c0002t0002g0076a0002c0002t0002g0077 | 2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.932-5568T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601688 | ||||||
chr6:46601817
|
G | A | 46 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(43): Show | 47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.932-5697C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46601817 | ||||||
chr6:46602023
|
C | T | 2 | a0002c0002t0001g0211a0002c0002t0001g0212 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.932-5903G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602023 | ||||||
chr6:46602072
|
C | G | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-5952G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602072 | ||||||
chr6:46602147
|
AATGGATG others(9): Show |
A | 5 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0117others(2): Show | 5 | HG02083.hp1 NA18945.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-6043_932-6028d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602147 | ||||||
chr6:46602238
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-6118T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602238 | ||||||
chr6:46602250
|
T | C | 2 | a0005c0004t0001g0279a0005c0004t0001g0283 | 2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.932-6130A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602250 | ||||||
chr6:46602289
|
G | T | 3 | a0002c0002t0002g0300a0002c0002t0002g0301a0002c0002t0002g0302 | 3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.932-6169C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602289 | ||||||
chr6:46602336
|
T | C | 25 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(22): Show | 25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-6216A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602336 | ||||||
chr6:46602379
|
T | G | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-6259A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602379 | ||||||
chr6:46602578
|
C | T | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932-6458G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602578 | ||||||
chr6:46602641
|
C | T | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-6521G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602641 | ||||||
chr6:46602684
|
C | T | 224 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(221): Show | 225 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.932-6564G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602684 | ||||||
chr6:46602689
|
C | CA | 19 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0122others(16): Show | 19 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.932-6570dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | ||||||
chr6:46602689
|
CA | C | 63 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.932-6570delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | ||||||
chr6:46602689
|
CAA | C | 9 | a0001c0001t0001g0124a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.932-6571_932-6570d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | ||||||
chr6:46602689
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0002g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.932-6581_932-6570d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602689 | ||||||
chr6:46602723
|
T | G | 1 | a0005c0004t0001g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.932-6603A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602723 | ||||||
chr6:46602806
|
T | C | 1 | a0003c0003t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.932-6686A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602806 | ||||||
chr6:46602901
|
C | T | 2 | a0007c0007t0002g0033a0007c0007t0002g0035 | 2 | HG01433.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.932-6781G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602901 | ||||||
chr6:46602923
|
T | TG | 180 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(177): Show | 181 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.932-6804dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602923 | ||||||
chr6:46602923
|
T | TGG | 63 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0053others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.932-6805_932-6804d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602923 | ||||||
chr6:46602925
|
G | GC | 4 | a0001c0001t0001g0066a0002c0002t0001g0120a0002c0002t0001g0169others(1): Show | 4 | HG01175.hp2 HG02965.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-6806_932-6805i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602925 | ||||||
chr6:46602933
|
G | GA | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-6814dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46602933 | ||||||
chr6:46603019
|
A | G | 2 | a0005c0004t0001g0268a0005c0004t0001g0270 | 2 | NA19068.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.932-6899T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603019 | ||||||
chr6:46603046
|
C | G | 224 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(221): Show | 225 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.932-6926G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603046 | ||||||
chr6:46603119
|
T | C | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-6999A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603119 | ||||||
chr6:46603167
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.932-7047G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603167 | ||||||
chr6:46603236
|
A | C | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-7116T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603236 | ||||||
chr6:46603451
|
C | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-7331G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603451 | ||||||
chr6:46603467
|
T | A | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7347A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603467 | ||||||
chr6:46603469
|
C | T | 1 | a0002c0002t0002g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.932-7349G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603469 | ||||||
chr6:46603538
|
C | T | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7418G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603538 | ||||||
chr6:46603539
|
T | C | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7419A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603539 | ||||||
chr6:46603541
|
C | T | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-7421G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603541 | ||||||
chr6:46603691
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-7571A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603691 | ||||||
chr6:46603724
|
G | C | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7604C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603724 | ||||||
chr6:46603802
|
T | C | 25 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(22): Show | 25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-7682A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46603802 | ||||||
chr6:46604176
|
AGAGCAAA others(7): Show |
A | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-8070_932-8057d others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604176 | ||||||
chr6:46604334
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.932-8214G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604334 | ||||||
chr6:46604354
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.932-8234G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604354 | ||||||
chr6:46604560
|
C | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8440G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604560 | ||||||
chr6:46604560
|
C | T | 2 | a0002c0002t0001g0253a0002c0002t0001g0266 | 2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.932-8440G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604560 | ||||||
chr6:46604723
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0223 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.932-8603G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604723 | ||||||
chr6:46604749
|
A | T | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-8629T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604749 | ||||||
chr6:46604791
|
A | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-8671T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604791 | ||||||
chr6:46604807
|
C | T | 1 | a0007c0007t0002g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.932-8687G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604807 | ||||||
chr6:46604939
|
T | C | 1 | a0005c0004t0001g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.932-8819A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604939 | ||||||
chr6:46604982
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-8862G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46604982 | ||||||
chr6:46605052
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-8932G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605052 | ||||||
chr6:46605084
|
C | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8964G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605084 | ||||||
chr6:46605391
|
G | A | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-9271C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605391 | ||||||
chr6:46605399
|
C | A | 1 | a0003c0003t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.932-9279G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605399 | ||||||
chr6:46605509
|
A | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-9389T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605509 | ||||||
chr6:46605536
|
G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG00735.hp2 HG01993.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.932-9416C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605536 | ||||||
chr6:46605573
|
G | A | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-9453C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605573 | ||||||
chr6:46605705
|
A | G | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.932-9585T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605705 | ||||||
chr6:46605748
|
T | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-9628A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605748 | ||||||
chr6:46605943
|
G | A | 1 | a0005c0004t0001g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.932-9823C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605943 | ||||||
chr6:46605966
|
A | T | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.932-9846T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46605966 | ||||||
chr6:46606167
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.932-10047G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606167 | ||||||
chr6:46606238
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-10118A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606238 | ||||||
chr6:46606378
|
C | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-10258G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606378 | ||||||
chr6:46606540
|
A | G | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932-10420T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606540 | ||||||
chr6:46606568
|
A | AC | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-10449dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606568 | ||||||
chr6:46606701
|
G | T | 1 | a0005c0004t0001g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.932-10581C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606701 | ||||||
chr6:46606710
|
G | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-10590C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606710 | ||||||
chr6:46606730
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.932-10610C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46606730 | ||||||
chr6:46607004
|
C | A | 6 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-10884G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607004 | ||||||
chr6:46607067
|
G | C | 25 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(22): Show | 25 | HG00741.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-10947C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607067 | ||||||
chr6:46607125
|
T | C | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.932-11005A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607125 | ||||||
chr6:46607153
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.932-11033C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607153 | ||||||
chr6:46607203
|
A | C | 1 | a0002c0002t0002g0151 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.932-11083T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607203 | ||||||
chr6:46607241
|
A | C | 1 | a0003c0003t0001g0201 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.932-11121T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607241 | ||||||
chr6:46607430
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-11310G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607430 | ||||||
chr6:46607464
|
T | TAC | 56 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.932-11346_932-1134 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | ||||||
chr6:46607464
|
T | TACAC | 21 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(18): Show | 21 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.932-11348_932-1134 others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | ||||||
chr6:46607464
|
T | TACACAC | 14 | a0001c0001t0001g0224a0001c0001t0001g0290a0001c0001t0001g0291others(11): Show | 14 | HG00741.hp1 HG02572.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.932-11350_932-1134 others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607464 | ||||||
chr6:46607514
|
G | GT | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-11395dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607514 | ||||||
chr6:46607531
|
C | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-11411G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607531 | ||||||
chr6:46607563
|
T | G | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-11443A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607563 | ||||||
chr6:46607565
|
C | T | 4 | a0002c0002t0001g0156a0002c0002t0001g0157a0003c0003t0001g0048others(1): Show | 4 | HG01952.hp2 HG01975.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-11445G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607565 | ||||||
chr6:46607659
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.932-11539A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46607659 | ||||||
chr6:46608233
|
T | C | 170 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.932-12113A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608233 | ||||||
chr6:46608475
|
A | T | 1 | a0005c0004t0001g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.932-12355T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608475 | ||||||
chr6:46608559
|
C | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(30): Show | 33 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-12439G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608559 | ||||||
chr6:46608624
|
T | A | 1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.932-12504A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608624 | ||||||
chr6:46608746
|
C | A | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.932-12626G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608746 | ||||||
chr6:46608834
|
G | A | 6 | a0002c0002t0002g0191a0002c0002t0002g0236a0002c0002t0002g0256others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-12714C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608834 | ||||||
chr6:46608927
|
A | G | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.932-12807T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608927 | ||||||
chr6:46608948
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-12828G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46608948 | ||||||
chr6:46609058
|
A | G | 2 | a0002c0002t0001g0120a0002c0002t0006g0110 | 2 | HG01175.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.932-12938T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609058 | ||||||
chr6:46609113
|
T | C | 2 | a0002c0002t0001g0210a0002c0002t0001g0220 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.932-12993A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609113 | ||||||
chr6:46609162
|
G | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-13042C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609162 | ||||||
chr6:46609215
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.932-13095G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609215 | ||||||
chr6:46609316
|
T | C | 3 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190 | 3 | HG03540.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.932-13196A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609316 | ||||||
chr6:46609349
|
G | GCTGAGTC others(7): Show |
1 | a0002c0002t0002g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.932-13243_932-1323 others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609349 | ||||||
chr6:46609349
|
GCTGAGTC others(7): Show |
G | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.932-13243_932-1323 others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609349 | ||||||
chr6:46609359
|
C | T | 1 | a0005c0004t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.932-13239G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609359 | ||||||
chr6:46609414
|
C | CA | 12 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 12 | HG01175.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-13295dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609414 | ||||||
chr6:46609475
|
A | C | 1 | a0002c0002t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.932-13355T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609475 | ||||||
chr6:46609763
|
A | G | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-13643T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46609763 | ||||||
chr6:46610042
|
G | A | 1 | a0002c0002t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-13922C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610042 | ||||||
chr6:46610092
|
A | G | 1 | a0004c0005t0001g0044 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.932-13972T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610092 | ||||||
chr6:46610167
|
T | G | 1 | a0005c0004t0001g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.932-14047A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610167 | ||||||
chr6:46610307
|
G | A | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.932-14187C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610307 | ||||||
chr6:46610350
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.932-14230G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610350 | ||||||
chr6:46610410
|
T | C | 6 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(3): Show | 6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-14290A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610410 | ||||||
chr6:46610731
|
G | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-14611C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610731 | ||||||
chr6:46610983
|
G | A | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+14435C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46610983 | ||||||
chr6:46611002
|
A | G | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+14416T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611002 | ||||||
chr6:46611116
|
G | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+14302C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611116 | ||||||
chr6:46611313
|
C | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+14105G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611313 | ||||||
chr6:46611399
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | NA18942.hp1 NA18977.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.931+14019T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611399 | ||||||
chr6:46611470
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+13948G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611470 | ||||||
chr6:46611479
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+13939T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611479 | ||||||
chr6:46611705
|
C | A | 4 | a0002c0002t0001g0194a0002c0002t0001g0198a0002c0002t0002g0101others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+13713G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46611705 | ||||||
chr6:46612119
|
C | T | 4 | a0001c0001t0001g0134a0002c0002t0001g0253a0002c0002t0001g0266others(1): Show | 4 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+13299G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612119 | ||||||
chr6:46612265
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.931+13153A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612265 | ||||||
chr6:46612287
|
G | T | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+13131C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612287 | ||||||
chr6:46612297
|
T | C | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+13121A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612297 | ||||||
chr6:46612322
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+13096C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612322 | ||||||
chr6:46612607
|
ATGTGAGA others(3): Show |
A | 1 | a0001c0001t0001g0240 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.931+12801_931+1281 others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612607 | ||||||
chr6:46612645
|
G | A | 171 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.931+12773C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612645 | ||||||
chr6:46612716
|
T | G | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+12702A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46612716 | ||||||
chr6:46613165
|
G | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+12253C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613165 | ||||||
chr6:46613170
|
T | A | 1 | a0008c0008t0002g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.931+12248A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613170 | ||||||
chr6:46613364
|
C | T | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+12054G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613364 | ||||||
chr6:46613395
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+12023G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613395 | ||||||
chr6:46613450
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.931+11968A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613450 | ||||||
chr6:46613473
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+11945A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613473 | ||||||
chr6:46613704
|
G | GTT | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+11712_931+1171 others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613704 | ||||||
chr6:46613871
|
G | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.931+11547C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613871 | ||||||
chr6:46613939
|
C | CA | 19 | a0002c0002t0001g0113a0002c0002t0001g0153a0002c0002t0001g0155others(16): Show | 19 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.931+11478dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613939 | ||||||
chr6:46613939
|
CA | C | 166 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(163): Show | 167 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.931+11478delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613939 | ||||||
chr6:46613945
|
A | G | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+11473T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46613945 | ||||||
chr6:46614012
|
A | G | 1 | a0002c0002t0002g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.931+11406T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614012 | ||||||
chr6:46614142
|
T | C | 2 | a0002c0002t0001g0080a0002c0002t0001g0084 | 2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.931+11276A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614142 | ||||||
chr6:46614180
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+11238A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614180 | ||||||
chr6:46614243
|
C | G | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+11175G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614243 | ||||||
chr6:46614250
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.931+11168A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614250 | ||||||
chr6:46614342
|
T | G | 46 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(43): Show | 47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.931+11076A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614342 | ||||||
chr6:46614396
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+11022G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614396 | ||||||
chr6:46614419
|
G | T | 128 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+10999C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614419 | ||||||
chr6:46614530
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.931+10888C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614530 | ||||||
chr6:46614580
|
T | A | 1 | a0002c0002t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.931+10838A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614580 | ||||||
chr6:46614674
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.931+10744G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614674 | ||||||
chr6:46614717
|
GA | G | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+10700delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614717 | ||||||
chr6:46614900
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+10518A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46614900 | ||||||
chr6:46615174
|
C | T | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+10244G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615174 | ||||||
chr6:46615237
|
ATATAT | A | 46 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(43): Show | 47 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.931+10176_931+1018 others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615237 | ||||||
chr6:46615253
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.931+10165A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615253 | ||||||
chr6:46615384
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+10034C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615384 | ||||||
chr6:46615399
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+10019C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615399 | ||||||
chr6:46615446
|
C | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9972G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615446 | ||||||
chr6:46615463
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+9955G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615463 | ||||||
chr6:46615576
|
C | T | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9842G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615576 | ||||||
chr6:46615584
|
C | T | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+9834G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615584 | ||||||
chr6:46615596
|
T | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9822A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615596 | ||||||
chr6:46615734
|
TA | T | 45 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(42): Show | 46 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.931+9683delT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615734 | ||||||
chr6:46615951
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+9467T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615951 | ||||||
chr6:46615973
|
A | G | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+9445T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46615973 | ||||||
chr6:46616005
|
T | TC | 10 | a0001c0001t0001g0177a0002c0002t0001g0109a0002c0002t0001g0163others(7): Show | 10 | HG01261.hp2 HG02027.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+9412dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616005 | ||||||
chr6:46616006
|
C | T | 1 | a0003c0003t0001g0196 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.931+9412G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616006 | ||||||
chr6:46616006
|
CCCCCCTC others(3): Show |
C | 119 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.931+9402_931+9411d others(12): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616006 | ||||||
chr6:46616016
|
T | TC | 149 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0131others(146): Show | 149 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.931+9401dupG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616016 | ||||||
chr6:46616016
|
T | TCC | 35 | a0001c0001t0001g0132a0001c0001t0001g0223a0002c0002t0001g0105others(32): Show | 35 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.931+9400_931+9401d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616016 | ||||||
chr6:46616042
|
CTTTCT | C | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+9371_931+9375d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616042 | ||||||
chr6:46616113
|
C | CTCTT | 3 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0003g0186 | 3 | HG00741.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.931+9301_931+9304d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616113 | ||||||
chr6:46616119
|
CT | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0224a0001c0001t0001g0227others(1): Show | 4 | NA18522.hp1 NA18978.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9298delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616119 | ||||||
chr6:46616123
|
T | C | 68 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.931+9295A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616123 | ||||||
chr6:46616124
|
C | T | 68 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.931+9294G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616124 | ||||||
chr6:46616125
|
TTTC | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0227a0001c0001t0001g0229others(1): Show | 4 | HG01952.hp2 NA18522.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9290_931+9292d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616125 | ||||||
chr6:46616140
|
CTTTCTTT others(16): Show |
C | 5 | a0002c0002t0001g0181a0002c0002t0002g0150a0002c0002t0002g0300others(2): Show | 5 | HG01192.hp2 HG02015.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9255_931+9277d others(25): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616140 | ||||||
chr6:46616144
|
CTTTCTTT others(12): Show |
C | 10 | a0002c0002t0002g0046a0002c0002t0002g0111a0002c0002t0002g0151others(7): Show | 10 | HG02165.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.931+9255_931+9273d others(21): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616144 | ||||||
chr6:46616148
|
CTTTCTTT others(8): Show |
C | 29 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0179others(26): Show | 30 | HG00597.hp1 HG00609.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.931+9255_931+9269d others(17): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616148 | ||||||
chr6:46616152
|
CTTTCTTT others(4): Show |
C | 35 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0097others(32): Show | 35 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.931+9255_931+9265d others(13): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616152 | ||||||
chr6:46616156
|
CTTTCTTT | C | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.931+9255_931+9261d others(9): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616156 | ||||||
chr6:46616160
|
CTTT | C | 54 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0063others(51): Show | 54 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.931+9255_931+9257d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616160 | ||||||
chr6:46616162
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9256A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616162 | ||||||
chr6:46616163
|
T | C | 40 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(37): Show | 40 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.931+9255A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TC | 42 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0060others(39): Show | 42 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TCTTTC | 13 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0235others(10): Show | 13 | HG00738.hp1 HG01071.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TCTTTCTT others(2): Show |
6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(11): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TCTTTCTT others(6): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0242others(3): Show | 6 | HG01258.hp1 HG01258.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9254_931+9255i others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TCTTTCTT others(10): Show |
2 | a0002c0002t0001g0220a0008c0008t0001g0015 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.931+9254_931+9255i others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616163
|
T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0243 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.931+9254_931+9255i others(23): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616163 | ||||||
chr6:46616164
|
T | A | 1 | a0001c0001t0001g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+9254A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616164 | ||||||
chr6:46616164
|
T | C | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0085others(20): Show | 23 | HG00140.hp2 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+9254A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616164 | ||||||
chr6:46616165
|
TTCTTTCT others(11): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9235_931+9252d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616165 | ||||||
chr6:46616166
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+9252A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616166 | ||||||
chr6:46616167
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9251G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616167 | ||||||
chr6:46616168
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0231 | 2 | NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.931+9250A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616168 | ||||||
chr6:46616168
|
T | TC | 14 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0082others(11): Show | 14 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+9249_931+9250i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616168 | ||||||
chr6:46616169
|
T | C | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0072others(20): Show | 23 | HG00280.hp1 HG00408.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.931+9249A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616169 | ||||||
chr6:46616170
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0231 | 2 | NA18949.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.931+9248A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616170 | ||||||
chr6:46616171
|
C | T | 37 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(34): Show | 37 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.931+9247G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616171 | ||||||
chr6:46616172
|
T | A | 14 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0082others(11): Show | 14 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+9246A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | ||||||
chr6:46616172
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0231 | 2 | NA18949.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.931+9246A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | ||||||
chr6:46616172
|
T | TC | 5 | a0001c0001t0001g0139a0001c0001t0001g0263a0006c0006t0001g0008others(2): Show | 5 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9245_931+9246i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616172 | ||||||
chr6:46616173
|
T | A | 23 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0072others(20): Show | 23 | HG00280.hp1 HG00408.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.931+9245A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616173 | ||||||
chr6:46616173
|
T | C | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0085others(14): Show | 17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9245A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616173 | ||||||
chr6:46616174
|
T | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0082others(13): Show | 16 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+9244A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616174 | ||||||
chr6:46616175
|
C | T | 22 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0085others(19): Show | 22 | HG00140.hp2 HG01175.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+9243G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616175 | ||||||
chr6:46616175
|
CTTT | C | 22 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0072others(19): Show | 22 | HG00408.hp2 HG01884.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.931+9240_931+9242d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616175 | ||||||
chr6:46616176
|
T | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0263a0006c0006t0001g0008others(2): Show | 5 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9242A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616176 | ||||||
chr6:46616176
|
T | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0082others(13): Show | 16 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+9242A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616176 | ||||||
chr6:46616177
|
T | A | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0085others(14): Show | 17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9241A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616177 | ||||||
chr6:46616177
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9241A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616177 | ||||||
chr6:46616178
|
T | C | 22 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0082others(19): Show | 22 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+9240A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616178 | ||||||
chr6:46616179
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9239G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616179 | ||||||
chr6:46616179
|
CTTT | C | 17 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0085others(14): Show | 17 | HG00140.hp2 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9236_931+9238d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616179 | ||||||
chr6:46616180
|
T | C | 44 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(41): Show | 44 | HG00408.hp2 HG00609.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+9238A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616180 | ||||||
chr6:46616181
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9237A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616181 | ||||||
chr6:46616181
|
T | C | 1 | a0002c0002t0004g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.931+9237A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616181 | ||||||
chr6:46616182
|
T | C | 45 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(42): Show | 45 | HG00408.hp2 HG00609.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.931+9236A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616182 | ||||||
chr6:46616183
|
C | T | 1 | a0008c0008t0002g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.931+9235G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616183 | ||||||
chr6:46616183
|
CT | C | 3 | a0001c0001t0001g0122a0002c0002t0002g0127a0002c0002t0004g0307 | 3 | HG00733.hp2 HG02055.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.931+9234delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616183 | ||||||
chr6:46616184
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931+9234A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616184 | ||||||
chr6:46616184
|
T | C | 62 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(59): Show | 62 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.931+9234A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616184 | ||||||
chr6:46616186
|
T | C | 64 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.931+9232A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616186 | ||||||
chr6:46616187
|
C | CT | 6 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(3): Show | 6 | HG02055.hp1 HG02886.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9230dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616187 | ||||||
chr6:46616187
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+9231G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616187 | ||||||
chr6:46616188
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+9230A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616188 | ||||||
chr6:46616188
|
T | C | 66 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.931+9230A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616188 | ||||||
chr6:46616190
|
C | T | 2 | a0001c0001t0003g0190a0002c0002t0002g0127 | 2 | HG00733.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9228G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616190 | ||||||
chr6:46616191
|
T | C | 71 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.931+9227A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616191 | ||||||
chr6:46616191
|
T | TTTCTCTT others(5): Show |
4 | a0001c0001t0001g0290a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9226_931+9227i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616191 | ||||||
chr6:46616192
|
T | C | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+9226A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
T | TTCCC | 26 | a0002c0002t0001g0094a0002c0002t0001g0160a0002c0002t0001g0176others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.931+9222_931+9225d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCC | T | 42 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(39): Show | 42 | HG00558.hp2 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.931+9222_931+9225d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(1): Show |
T | 53 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(50): Show | 54 | HG00597.hp2 HG00639.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.931+9218_931+9225d others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(5): Show |
T | 17 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0086others(14): Show | 17 | HG00735.hp2 HG01069.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+9214_931+9225d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(9): Show |
T | 8 | a0001c0001t0001g0053a0002c0002t0002g0102a0002c0002t0002g0146others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+9210_931+9225d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(11): Show |
T | 1 | a0004c0005t0001g0017 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.931+9208_931+9225d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(13): Show |
T | 6 | a0001c0001t0003g0277a0005c0004t0001g0233a0005c0004t0001g0284others(3): Show | 6 | HG02647.hp1 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9206_931+9225d others(22): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(17): Show |
T | 1 | a0001c0001t0003g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+9202_931+9225d others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616192
|
TTCCCTCC others(21): Show |
T | 1 | a0004c0005t0001g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.931+9198_931+9225d others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616192 | ||||||
chr6:46616193
|
TCCCTCCC others(6): Show |
T | 2 | a0001c0001t0003g0187a0001c0001t0003g0189 | 2 | HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.931+9212_931+9224d others(15): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616193 | ||||||
chr6:46616193
|
TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.931+9208_931+9224d others(19): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616193 | ||||||
chr6:46616194
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9224G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616194 | ||||||
chr6:46616195
|
C | T | 1 | a0003c0003t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.931+9223G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616195 | ||||||
chr6:46616196
|
C | T | 2 | a0001c0001t0003g0190a0002c0002t0001g0194 | 2 | NA18972.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9222G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616196 | ||||||
chr6:46616198
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9220G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616198 | ||||||
chr6:46616200
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9218G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616200 | ||||||
chr6:46616202
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931+9216G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616202 | ||||||
chr6:46616204
|
C | T | 2 | a0001c0001t0003g0190a0005c0004t0001g0275 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9214G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616204 | ||||||
chr6:46616206
|
C | T | 2 | a0001c0001t0003g0190a0005c0004t0001g0275 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9212G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616206 | ||||||
chr6:46616208
|
C | T | 4 | a0001c0001t0003g0187a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | HG02886.hp2 HG03540.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9210G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616208 | ||||||
chr6:46616210
|
C | CCCTTCCT others(5): Show |
2 | a0001c0001t0001g0262a0006c0006t0001g0007 | 2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.931+9207_931+9208i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616210 | ||||||
chr6:46616210
|
C | T | 3 | a0001c0001t0003g0189a0001c0001t0003g0190a0005c0004t0001g0275 | 3 | HG02886.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.931+9208G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616210 | ||||||
chr6:46616211
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.931+9207G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616211 | ||||||
chr6:46616212
|
C | T | 6 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(3): Show | 6 | HG02027.hp1 HG02886.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9206G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616212 | ||||||
chr6:46616214
|
C | CCCTTCCT others(1): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0231a0001c0001t0001g0255others(1): Show | 4 | HG01175.hp1 NA18942.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9203_931+9204i others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | ||||||
chr6:46616214
|
C | CCCTTCCT others(5): Show |
2 | a0001c0001t0001g0230a0006c0006t0001g0043 | 2 | HG00609.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.931+9203_931+9204i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | ||||||
chr6:46616214
|
C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0249a0001c0001t0001g0254 | 2 | NA18962.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.931+9203_931+9204i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | ||||||
chr6:46616214
|
C | CCCTTCCT others(17): Show |
1 | a0001c0001t0001g0124 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.931+9203_931+9204i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | ||||||
chr6:46616214
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0247a0001c0001t0001g0262others(1): Show | 4 | HG00738.hp2 HG02074.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9204G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616214 | ||||||
chr6:46616215
|
C | T | 6 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(3): Show | 6 | HG02886.hp2 HG03540.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9203G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616215 | ||||||
chr6:46616216
|
C | T | 4 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0190others(1): Show | 4 | HG02886.hp2 HG03540.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9202G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616216 | ||||||
chr6:46616218
|
C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0263 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.931+9199_931+9200i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | ||||||
chr6:46616218
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0126 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.931+9199_931+9200i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | ||||||
chr6:46616218
|
C | CCCTTCCT others(17): Show |
2 | a0001c0001t0001g0260a0006c0006t0001g0023 | 2 | HG00140.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.931+9199_931+9200i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | ||||||
chr6:46616218
|
C | CCCTTCCT others(21): Show |
1 | a0001c0001t0001g0123 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.931+9199_931+9200i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | ||||||
chr6:46616218
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0124others(13): Show | 16 | HG00280.hp1 HG00609.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.931+9200G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616218 | ||||||
chr6:46616219
|
C | T | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9199G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616219 | ||||||
chr6:46616220
|
C | A | 2 | a0001c0001t0003g0187a0001c0001t0003g0277 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.931+9198G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616220 | ||||||
chr6:46616222
|
C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.931+9195_931+9196i others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.931+9195_931+9196i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | CCCTTCCT others(17): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0229a0006c0006t0001g0004 | 3 | HG01261.hp1 NA18963.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | CCCTTCCT others(21): Show |
2 | a0001c0001t0001g0246a0006c0006t0001g0006 | 2 | HG02738.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | CCCTTCCT others(25): Show |
2 | a0001c0001t0001g0227a0001c0001t0001g0234 | 2 | NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | CCCTTCCT others(29): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0251 | 2 | NA18954.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.931+9195_931+9196i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616222
|
C | T | 26 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0093others(23): Show | 26 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.931+9196G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616222 | ||||||
chr6:46616223
|
C | T | 5 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0189others(2): Show | 5 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9195G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616223 | ||||||
chr6:46616224
|
C | A | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9194G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616224 | ||||||
chr6:46616226
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.931+9191_931+9192i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | ||||||
chr6:46616226
|
C | CCCTTCCT others(17): Show |
2 | a0001c0001t0001g0232a0001c0001t0001g0239 | 2 | NA18995.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | ||||||
chr6:46616226
|
C | CCCTTCCT others(21): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0125 | 2 | HG02976.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | ||||||
chr6:46616226
|
C | CCCTTCCT others(25): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | NA18959.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.931+9191_931+9192i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | ||||||
chr6:46616226
|
C | T | 32 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0091others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.931+9192G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616226 | ||||||
chr6:46616228
|
C | A | 5 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0189others(2): Show | 5 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9190G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616228 | ||||||
chr6:46616230
|
C | CCCTTCCT others(25): Show |
1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | ||||||
chr6:46616230
|
C | CCCTTCCT others(29): Show |
1 | a0001c0001t0001g0261 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | ||||||
chr6:46616230
|
C | CCCTTCCT others(33): Show |
1 | a0004c0005t0001g0032 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.931+9187_931+9188i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | ||||||
chr6:46616230
|
C | T | 41 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0081others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.931+9188G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616230 | ||||||
chr6:46616234
|
C | T | 46 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0071others(43): Show | 46 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.931+9184G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616234 | ||||||
chr6:46616238
|
C | T | 51 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0069others(48): Show | 51 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.931+9180G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616238 | ||||||
chr6:46616242
|
C | CCCTCCCT others(37): Show |
1 | a0001c0001t0001g0291 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(46): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | CCCTCCCT others(29): Show |
1 | a0001c0001t0001g0293 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | CCCTCCCT others(21): Show |
2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.931+9175_931+9176i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | CCCTCCCT others(25): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.931+9175_931+9176i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | CCCTTCCT others(29): Show |
1 | a0001c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+9175_931+9176i others(38): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | CCCTTCCT others(33): Show |
1 | a0001c0001t0001g0228 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.931+9175_931+9176i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616242
|
C | T | 114 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.931+9176G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616242 | ||||||
chr6:46616255
|
C | T | 1 | a0005c0004t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.931+9163G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616255 | ||||||
chr6:46616259
|
T | C | 78 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.931+9159A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616259 | ||||||
chr6:46616282
|
T | TCCTTCCT others(9): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0082 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.931+9135_931+9136i others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | ||||||
chr6:46616282
|
T | TCCTTCCT others(17): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0081a0001c0001t0001g0083others(1): Show | 4 | HG03130.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(26): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | ||||||
chr6:46616282
|
T | TCCTTCCT others(21): Show |
4 | a0001c0001t0001g0104a0001c0001t0001g0138a0001c0001t0001g0183others(1): Show | 4 | HG02572.hp2 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(30): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | ||||||
chr6:46616282
|
T | TCCTTCCT others(25): Show |
5 | a0001c0001t0001g0050a0001c0001t0001g0069a0001c0001t0001g0070others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(34): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | ||||||
chr6:46616282
|
T | TCCTTCCT others(33): Show |
5 | a0001c0001t0001g0068a0001c0001t0001g0085a0001c0001t0001g0089others(2): Show | 5 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9135_931+9136i others(42): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616282 | ||||||
chr6:46616311
|
G | A | 6 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(3): Show | 6 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+9107C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616311 | ||||||
chr6:46616362
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+9056T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616362 | ||||||
chr6:46616531
|
C | A | 1 | a0004c0009t0001g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.931+8887G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616531 | ||||||
chr6:46616574
|
T | G | 1 | a0002c0002t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.931+8844A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616574 | ||||||
chr6:46616587
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.931+8831A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616587 | ||||||
chr6:46616706
|
A | C | 43 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(40): Show | 44 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+8712T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616706 | ||||||
chr6:46616738
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.931+8680A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616738 | ||||||
chr6:46616855
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.931+8563A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616855 | ||||||
chr6:46616949
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+8469A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616949 | ||||||
chr6:46616953
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+8465G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46616953 | ||||||
chr6:46617140
|
T | G | 1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.931+8278A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617140 | ||||||
chr6:46617286
|
C | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+8132G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617286 | ||||||
chr6:46617356
|
T | G | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+8062A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617356 | ||||||
chr6:46617409
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.931+8009T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617409 | ||||||
chr6:46617416
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+8002G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617416 | ||||||
chr6:46617454
|
G | A | 43 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(40): Show | 44 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+7964C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617454 | ||||||
chr6:46617661
|
G | A | 1 | a0004c0009t0001g0028 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.931+7757C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617661 | ||||||
chr6:46617737
|
G | A | 1 | a0002c0002t0002g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.931+7681C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617737 | ||||||
chr6:46617855
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.931+7563A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46617855 | ||||||
chr6:46618165
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.931+7253G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618165 | ||||||
chr6:46618175
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+7243G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618175 | ||||||
chr6:46618421
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+6997T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618421 | ||||||
chr6:46618534
|
A | G | 8 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(5): Show | 8 | HG01884.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.931+6884T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618534 | ||||||
chr6:46618576
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.931+6842G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618576 | ||||||
chr6:46618812
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+6606A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618812 | ||||||
chr6:46618915
|
T | C | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+6503A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618915 | ||||||
chr6:46618973
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.931+6445G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46618973 | ||||||
chr6:46619008
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+6410A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619008 | ||||||
chr6:46619203
|
C | T | 1 | a0003c0003t0001g0215 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.931+6215G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619203 | ||||||
chr6:46619462
|
T | C | 1 | a0002c0002t0002g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.931+5956A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619462 | ||||||
chr6:46619783
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5635G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619783 | ||||||
chr6:46619913
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5505G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619913 | ||||||
chr6:46619927
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5491G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46619927 | ||||||
chr6:46620096
|
C | A | 13 | a0002c0002t0001g0113a0002c0002t0001g0169a0002c0002t0001g0170others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.931+5322G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620096 | ||||||
chr6:46620149
|
T | C | 1 | a0007c0007t0002g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.931+5269A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620149 | ||||||
chr6:46620179
|
T | C | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+5239A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620179 | ||||||
chr6:46620235
|
C | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5183G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620235 | ||||||
chr6:46620260
|
C | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5158G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620260 | ||||||
chr6:46620290
|
G | T | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.931+5128C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620290 | ||||||
chr6:46620312
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+5106G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620312 | ||||||
chr6:46620625
|
T | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4793A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620625 | ||||||
chr6:46620668
|
TG | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4749delC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620668 | ||||||
chr6:46620684
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4734G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620684 | ||||||
chr6:46620733
|
G | A | 1 | a0005c0004t0001g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931+4685C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620733 | ||||||
chr6:46620897
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4521T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620897 | ||||||
chr6:46620899
|
A | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4519T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620899 | ||||||
chr6:46620905
|
ACAAT | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4509_931+4512d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620905 | ||||||
chr6:46620915
|
A | G | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931+4503T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620915 | ||||||
chr6:46620966
|
G | A | 1 | a0004c0005t0001g0036 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+4452C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46620966 | ||||||
chr6:46621089
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.931+4329C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621089 | ||||||
chr6:46621202
|
G | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4216C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621202 | ||||||
chr6:46621216
|
T | TCA | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4201_931+4202i others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621216 | ||||||
chr6:46621231
|
T | C | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+4187A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621231 | ||||||
chr6:46621318
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+4100T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621318 | ||||||
chr6:46621323
|
AAAATT | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+4090_931+4094d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621323 | ||||||
chr6:46621422
|
G | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3996C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621422 | ||||||
chr6:46621434
|
A | G | 1 | a0002c0002t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.931+3984T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621434 | ||||||
chr6:46621490
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3928G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621490 | ||||||
chr6:46621513
|
G | T | 1 | a0005c0004t0001g0192 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.931+3905C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621513 | ||||||
chr6:46621546
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3872G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621546 | ||||||
chr6:46621558
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931+3860A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621558 | ||||||
chr6:46621606
|
C | G | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+3812G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621606 | ||||||
chr6:46621742
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+3676T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621742 | ||||||
chr6:46621764
|
C | G | 128 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+3654G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621764 | ||||||
chr6:46621765
|
C | A | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+3653G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621765 | ||||||
chr6:46621816
|
T | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3602A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621816 | ||||||
chr6:46621958
|
T | C | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.931+3460A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46621958 | ||||||
chr6:46622008
|
G | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3410C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622008 | ||||||
chr6:46622066
|
A | C | 1 | a0002c0002t0001g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.931+3352T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622066 | ||||||
chr6:46622071
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3347G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622071 | ||||||
chr6:46622155
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.931+3263G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622155 | ||||||
chr6:46622259
|
T | G | 1 | a0002c0002t0004g0307 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.931+3159A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622259 | ||||||
chr6:46622334
|
C | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+3084G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622334 | ||||||
chr6:46622440
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2978G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622440 | ||||||
chr6:46622471
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2947T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622471 | ||||||
chr6:46622523
|
G | A | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2895C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622523 | ||||||
chr6:46622560
|
C | CTATGATC others(55): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.931+2857_931+2858i others(64): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622560 | ||||||
chr6:46622577
|
T | C | 171 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.931+2841A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622577 | ||||||
chr6:46622693
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2725T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622693 | ||||||
chr6:46622943
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+2475G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622943 | ||||||
chr6:46622944
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.931+2474A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622944 | ||||||
chr6:46622966
|
T | A | 3 | a0002c0002t0002g0129a0003c0003t0002g0213a0003c0003t0002g0221 | 3 | HG00735.hp1 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.931+2452A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46622966 | ||||||
chr6:46623019
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2399T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623019 | ||||||
chr6:46623148
|
T | C | 41 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(38): Show | 42 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.931+2270A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623148 | ||||||
chr6:46623187
|
C | CA | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2230_931+2231i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623187 | ||||||
chr6:46623265
|
A | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+2153T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623265 | ||||||
chr6:46623302
|
T | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+2116A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623302 | ||||||
chr6:46623354
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931+2064A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623354 | ||||||
chr6:46623480
|
C | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+1938G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623480 | ||||||
chr6:46623836
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | NA18949.hp2 NA18963.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.931+1582A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623836 | ||||||
chr6:46623940
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+1478G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623940 | ||||||
chr6:46623983
|
C | T | 1 | a0004c0005t0001g0029 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.931+1435G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623983 | ||||||
chr6:46623984
|
A | AT | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+1433dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46623984 | ||||||
chr6:46624290
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+1128C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624290 | ||||||
chr6:46624361
|
C | T | 1 | a0002c0002t0002g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.931+1057G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624361 | ||||||
chr6:46624372
|
C | A | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+1046G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624372 | ||||||
chr6:46624428
|
A | G | 1 | a0001c0001t0003g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.931+990T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624428 | ||||||
chr6:46624452
|
T | C | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+966A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624452 | ||||||
chr6:46624501
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+917G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624501 | ||||||
chr6:46624564
|
A | G | 1 | a0002c0002t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.931+854T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624564 | ||||||
chr6:46624571
|
A | G | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+847T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624571 | ||||||
chr6:46624653
|
T | C | 7 | a0002c0002t0002g0102a0002c0002t0002g0168a0002c0002t0002g0274others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+765A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624653 | ||||||
chr6:46624681
|
T | C | 44 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+737A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624681 | ||||||
chr6:46624776
|
A | T | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+642T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624776 | ||||||
chr6:46624886
|
C | T | 69 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.931+532G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624886 | ||||||
chr6:46624889
|
C | T | 128 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.931+529G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624889 | ||||||
chr6:46624946
|
C | T | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.931+472G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46624946 | ||||||
chr6:46625142
|
G | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+276C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625142 | ||||||
chr6:46625152
|
T | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.931+266A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625152 | ||||||
chr6:46625290
|
T | C | 1 | a0004c0005t0001g0036 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+128A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625290 | ||||||
chr6:46625339
|
A | G | 1 | a0007c0007t0001g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.931+79T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625339 | ||||||
chr6:46625342
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.931+76C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625342 | ||||||
chr6:46625349
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.931+69T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 7/11 | chr6 | 46625349 | ||||||
chr6:46625535
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.841-27T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625535 | ||||||
chr6:46625584
|
C | T | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-76G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625584 | ||||||
chr6:46625759
|
A | G | 1 | a0002c0002t0001g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.841-251T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625759 | ||||||
chr6:46625815
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.841-307T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625815 | ||||||
chr6:46625870
|
A | G | 1 | a0002c0002t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.841-362T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46625870 | ||||||
chr6:46626061
|
C | CT | 68 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.841-554dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626061 | ||||||
chr6:46626099
|
A | T | 77 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.841-591T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626099 | ||||||
chr6:46626329
|
T | C | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-821A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626329 | ||||||
chr6:46626384
|
G | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.841-876C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626384 | ||||||
chr6:46626803
|
A | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-1295T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626803 | ||||||
chr6:46626908
|
T | C | 23 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(20): Show | 23 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-1400A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626908 | ||||||
chr6:46626909
|
G | A | 23 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(20): Show | 23 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-1401C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626909 | ||||||
chr6:46626912
|
T | C | 16 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(13): Show | 16 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1404A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46626912 | ||||||
chr6:46627080
|
A | G | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02886.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.841-1572T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627080 | ||||||
chr6:46627208
|
C | T | 2 | a0001c0001t0001g0045a0006c0006t0001g0001 | 3 | HG02056.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.841-1700G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627208 | ||||||
chr6:46627243
|
C | G | 56 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.841-1735G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627243 | ||||||
chr6:46627344
|
A | G | 1 | a0005c0004t0001g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.841-1836T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627344 | ||||||
chr6:46627380
|
C | G | 20 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0140others(17): Show | 20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1872G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627380 | ||||||
chr6:46627410
|
TTTTA | T | 30 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.841-1906_841-1903d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627410 | ||||||
chr6:46627418
|
ATTTAT | A | 67 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(64): Show | 68 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.841-1915_841-1911d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627418 | ||||||
chr6:46627419
|
TTTA | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0224a0001c0001t0001g0225others(13): Show | 16 | HG00741.hp1 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1914_841-1912d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627419 | ||||||
chr6:46627422
|
AT | A | 113 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.841-1915delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | ||||||
chr6:46627422
|
ATTTTT | A | 24 | a0003c0003t0001g0259a0004c0005t0001g0010a0004c0005t0001g0012others(21): Show | 24 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-1919_841-1915d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | ||||||
chr6:46627422
|
ATTTTTT | A | 20 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0140others(17): Show | 20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1920_841-1915d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627422 | ||||||
chr6:46627426
|
T | A | 6 | a0001c0001t0001g0096a0001c0001t0001g0292a0003c0003t0001g0205others(3): Show | 6 | HG01071.hp1 HG01074.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-1918A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627426 | ||||||
chr6:46627427
|
T | A | 2 | a0002c0002t0001g0163a0002c0002t0002g0207 | 2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.841-1919A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627427 | ||||||
chr6:46627480
|
G | A | 1 | a0006c0006t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.841-1972C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627480 | ||||||
chr6:46627504
|
C | T | 20 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0140others(17): Show | 20 | HG01069.hp2 HG01255.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1996G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627504 | ||||||
chr6:46627505
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | NA18955.hp1 NA19002.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-1997C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627505 | ||||||
chr6:46627698
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.841-2190C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627698 | ||||||
chr6:46627750
|
A | T | 19 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0103others(16): Show | 19 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-2242T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627750 | ||||||
chr6:46627753
|
A | T | 57 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.841-2245T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627753 | ||||||
chr6:46627768
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.841-2260T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627768 | ||||||
chr6:46627777
|
A | G | 27 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0103others(24): Show | 27 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.841-2269T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46627777 | ||||||
chr6:46628068
|
C | A | 1 | a0002c0002t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.841-2560G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628068 | ||||||
chr6:46628120
|
G | C | 8 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-2612C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628120 | ||||||
chr6:46628184
|
G | C | 1 | a0007c0007t0002g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.841-2676C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628184 | ||||||
chr6:46628366
|
G | A | 2 | a0002c0002t0002g0168a0003c0003t0002g0257 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.840+2597C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628366 | ||||||
chr6:46628549
|
A | C | 66 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.840+2414T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628549 | ||||||
chr6:46628642
|
A | T | 19 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0103others(16): Show | 19 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.840+2321T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628642 | ||||||
chr6:46628780
|
C | T | 2 | a0002c0002t0002g0101a0002c0002t0002g0136 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.840+2183G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46628780 | ||||||
chr6:46629111
|
G | A | 1 | a0005c0004t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.840+1852C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629111 | ||||||
chr6:46629227
|
G | A | 1 | a0005c0004t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.840+1736C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629227 | ||||||
chr6:46629277
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.840+1686C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629277 | ||||||
chr6:46629525
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0010c0011t0001g0178 | 3 | HG02258.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.840+1438T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629525 | ||||||
chr6:46629771
|
T | C | 4 | a0002c0002t0001g0194a0002c0002t0001g0198a0002c0002t0002g0101others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1192A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629771 | ||||||
chr6:46629871
|
G | T | 27 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(24): Show | 27 | HG01069.hp2 HG01255.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.840+1092C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629871 | ||||||
chr6:46629903
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1060A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629903 | ||||||
chr6:46629918
|
G | A | 1 | a0002c0002t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.840+1045C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46629918 | ||||||
chr6:46630025
|
A | G | 26 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0103others(23): Show | 26 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.840+938T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630025 | ||||||
chr6:46630130
|
C | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0265others(1): Show | 4 | HG00741.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+833G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | ||||||
chr6:46630130
|
C | CAAAAA | 13 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0137others(10): Show | 13 | HG01069.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+828_840+832dup others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | ||||||
chr6:46630130
|
C | CAACAA | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0003g0186others(7): Show | 10 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+832_840+833ins others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630130 | ||||||
chr6:46630137
|
A | C | 8 | a0005c0004t0001g0282a0005c0004t0001g0284a0005c0004t0001g0286others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+826T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630137 | ||||||
chr6:46630142
|
C | CA | 8 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+820dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630142 | ||||||
chr6:46630526
|
A | G | 12 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0002g0238others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+437T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630526 | ||||||
chr6:46630672
|
A | C | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.840+291T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 6/11 | chr6 | 46630672 | ||||||
chr6:46631105
|
CTA | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0002g0238others(1): Show | 4 | HG02258.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-37_733-36delTA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631105 | ||||||
chr6:46631120
|
C | T | 13 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(10): Show | 13 | HG02109.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.733-50G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631120 | ||||||
chr6:46631450
|
A | G | 52 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.733-380T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631450 | ||||||
chr6:46631537
|
C | T | 8 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-467G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631537 | ||||||
chr6:46631803
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.733-733A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46631803 | ||||||
chr6:46632105
|
T | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0002g0238others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1035A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632105 | ||||||
chr6:46632326
|
A | G | 48 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(45): Show | 49 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.733-1256T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632326 | ||||||
chr6:46632350
|
A | G | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.733-1280T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632350 | ||||||
chr6:46632412
|
C | T | 1 | a0003c0003t0001g0281 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.733-1342G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632412 | ||||||
chr6:46632604
|
TC | T | 20 | a0004c0005t0001g0010a0004c0005t0001g0012a0004c0005t0001g0013others(17): Show | 20 | HG00609.hp2 HG02015.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.733-1535delG | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632604 | ||||||
chr6:46632610
|
C | T | 8 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-1540G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632610 | ||||||
chr6:46632705
|
AT | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0002g0238others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1636delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632705 | ||||||
chr6:46632954
|
A | G | 3 | a0003c0003t0001g0202a0003c0003t0001g0214a0007c0007t0001g0002 | 3 | HG02083.hp2 NA18975.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.733-1884T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632954 | ||||||
chr6:46632969
|
T | TAGAGACT others(315): Show |
1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733-1900_733-1899i others(324): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46632969 | ||||||
chr6:46633132
|
G | C | 1 | a0002c0002t0002g0046 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-2062C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633132 | ||||||
chr6:46633395
|
C | T | 1 | a0002c0002t0002g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.733-2325G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633395 | ||||||
chr6:46633578
|
G | T | 3 | a0002c0002t0002g0127a0002c0002t0002g0143a0002c0002t0002g0144 | 3 | HG00733.hp2 HG01975.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.733-2508C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633578 | ||||||
chr6:46633597
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.733-2527C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633597 | ||||||
chr6:46633614
|
T | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0002g0238others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-2544A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633614 | ||||||
chr6:46633617
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02280.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.733-2547C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633617 | ||||||
chr6:46633625
|
G | A | 3 | a0002c0002t0001g0051a0002c0002t0001g0112a0003c0003t0002g0272 | 3 | HG01496.hp2 HG01952.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.733-2555C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633625 | ||||||
chr6:46633631
|
G | A | 3 | a0002c0002t0001g0267a0008c0008t0001g0027a0008c0008t0002g0014 | 3 | HG01243.hp2 HG01496.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.733-2561C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633631 | ||||||
chr6:46633640
|
C | T | 8 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-2570G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633640 | ||||||
chr6:46633819
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.732+2570A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633819 | ||||||
chr6:46633844
|
A | C | 4 | a0001c0001t0001g0244a0001c0001t0001g0260a0001c0001t0001g0262others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+2545T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633844 | ||||||
chr6:46633848
|
C | G | 2 | a0003c0003t0001g0200a0003c0003t0001g0201 | 2 | HG01109.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.732+2541G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633848 | ||||||
chr6:46633863
|
G | GA | 11 | a0001c0001t0001g0166a0001c0001t0002g0238a0001c0001t0003g0186others(8): Show | 11 | HG02615.hp1 HG02886.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+2525dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46633863 | ||||||
chr6:46634175
|
G | A | 114 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(111): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.732+2214C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634175 | ||||||
chr6:46634267
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+2122C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634267 | ||||||
chr6:46634507
|
C | CT | 50 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(47): Show | 51 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.732+1881dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634507 | ||||||
chr6:46634523
|
G | GT | 26 | a0001c0001t0001g0061a0001c0001t0001g0121a0001c0001t0001g0185others(23): Show | 26 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(3): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | ||||||
chr6:46634523
|
G | GTT | 73 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(70): Show | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | ||||||
chr6:46634523
|
G | GTTT | 4 | a0001c0001t0001g0062a0001c0001t0001g0123a0001c0001t0001g0227others(1): Show | 4 | HG03688.hp1 NA18955.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+1865_732+1866i others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634523 | ||||||
chr6:46634524
|
C | T | 113 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(110): Show | 114 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.732+1865G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634524 | ||||||
chr6:46634524
|
CT | C | 72 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(69): Show | 72 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.732+1864delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634524 | ||||||
chr6:46634603
|
C | A | 1 | a0001c0001t0003g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732+1786G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634603 | ||||||
chr6:46634668
|
C | T | 2 | a0002c0002t0002g0101a0002c0002t0002g0136 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.732+1721G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634668 | ||||||
chr6:46634826
|
C | T | 147 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.732+1563G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46634826 | ||||||
chr6:46635123
|
T | C | 1 | a0004c0005t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.732+1266A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635123 | ||||||
chr6:46635145
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+1244A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635145 | ||||||
chr6:46635230
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+1159A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635230 | ||||||
chr6:46635301
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.732+1088G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635301 | ||||||
chr6:46635344
|
G | A | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.732+1045C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635344 | ||||||
chr6:46635441
|
C | A | 2 | a0002c0002t0001g0253a0002c0002t0001g0266 | 2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.732+948G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635441 | ||||||
chr6:46635479
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.732+910G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635479 | ||||||
chr6:46635531
|
C | T | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.732+858G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635531 | ||||||
chr6:46635542
|
G | GTGTT | 3 | a0001c0001t0001g0082a0001c0001t0001g0096a0002c0002t0001g0135 | 3 | HG02109.hp1 HG03453.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.732+843_732+846dup others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635542 | ||||||
chr6:46635583
|
G | A | 1 | a0005c0004t0001g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.732+806C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635583 | ||||||
chr6:46635728
|
A | T | 23 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(20): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+661T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635728 | ||||||
chr6:46635783
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.732+606C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635783 | ||||||
chr6:46635950
|
G | A | 147 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.732+439C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46635950 | ||||||
chr6:46636141
|
T | G | 1 | a0004c0005t0001g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.732+248A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636141 | ||||||
chr6:46636220
|
G | A | 3 | a0002c0002t0002g0168a0003c0003t0002g0257a0003c0003t0002g0272 | 3 | HG01891.hp2 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.732+169C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636220 | ||||||
chr6:46636263
|
G | C | 71 | a0002c0002t0001g0176a0003c0003t0001g0048a0003c0003t0001g0193others(68): Show | 71 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.732+126C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 5/11 | chr6 | 46636263 | ||||||
chr6:46636533
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.639-51A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636533 | ||||||
chr6:46636749
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.639-267T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636749 | ||||||
chr6:46636775
|
GGCTGCTG others(3): Show |
G | 1 | a0002c0002t0001g0210 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.639-303_639-294del others(10): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636775 | ||||||
chr6:46636821
|
A | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0002c0002t0002g0236others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-339T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636821 | ||||||
chr6:46636911
|
G | A | 3 | a0005c0004t0001g0237a0005c0004t0001g0258a0005c0004t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.639-429C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46636911 | ||||||
chr6:46637037
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.639-555T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637037 | ||||||
chr6:46637175
|
T | C | 21 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.638+654A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637175 | ||||||
chr6:46637360
|
A | T | 1 | a0007c0007t0001g0016 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.638+469T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637360 | ||||||
chr6:46637437
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638+392C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637437 | ||||||
chr6:46637463
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.638+366G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637463 | ||||||
chr6:46637605
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0002c0002t0002g0236others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+224C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637605 | ||||||
chr6:46637732
|
A | G | 9 | a0001c0001t0001g0292a0001c0001t0003g0186a0001c0001t0003g0187others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+97T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 4/11 | chr6 | 46637732 | ||||||
chr6:46638013
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | NA18960.hp1 NA18971.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-35C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638013 | ||||||
chr6:46638042
|
A | C | 28 | a0002c0002t0001g0176a0003c0003t0001g0048a0003c0003t0001g0259others(25): Show | 28 | HG00408.hp2 HG00609.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.489-64T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638042 | ||||||
chr6:46638105
|
G | A | 2 | a0003c0003t0001g0193a0003c0003t0001g0195 | 2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.489-127C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638105 | ||||||
chr6:46638137
|
G | C | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-159C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638137 | ||||||
chr6:46638394
|
C | T | 19 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0116others(16): Show | 19 | HG00741.hp1 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.489-416G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638394 | ||||||
chr6:46638534
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.489-556T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638534 | ||||||
chr6:46638591
|
T | C | 226 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(223): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.489-613A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638591 | ||||||
chr6:46638698
|
G | A | 8 | a0002c0002t0001g0113a0002c0002t0001g0169a0002c0002t0001g0170others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-720C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638698 | ||||||
chr6:46638708
|
C | T | 1 | a0010c0011t0001g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.489-730G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638708 | ||||||
chr6:46638813
|
G | A | 1 | a0005c0004t0001g0269 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.488+681C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638813 | ||||||
chr6:46638842
|
C | T | 3 | a0005c0004t0001g0237a0005c0004t0001g0258a0005c0004t0001g0271 | 3 | HG02451.hp2 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.488+652G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638842 | ||||||
chr6:46638877
|
G | A | 8 | a0002c0002t0001g0113a0002c0002t0001g0169a0002c0002t0001g0170others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+617C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638877 | ||||||
chr6:46638979
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.488+515G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46638979 | ||||||
chr6:46639330
|
T | C | 20 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(17): Show | 20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.488+164A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639330 | ||||||
chr6:46639335
|
C | CA | 16 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(13): Show | 16 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.488+158dupT | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639335 | ||||||
chr6:46639344
|
AT | A | 145 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(142): Show | 146 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.488+149delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639344 | ||||||
chr6:46639345
|
T | A | 9 | a0002c0002t0001g0113a0002c0002t0001g0169a0002c0002t0001g0170others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+149A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639345 | ||||||
chr6:46639488
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.488+6T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 3/11 | chr6 | 46639488 | ||||||
chr6:46639724
|
T | A | 1 | a0002c0002t0001g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.314-56A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639724 | ||||||
chr6:46639740
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.314-72T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639740 | ||||||
chr6:46639800
|
A | T | 1 | a0001c0001t0003g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.314-132T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639800 | ||||||
chr6:46639826
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-158A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639826 | ||||||
chr6:46639833
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.314-165C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639833 | ||||||
chr6:46639834
|
A | G | 20 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(17): Show | 20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-166T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639834 | ||||||
chr6:46639841
|
G | C | 48 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.314-173C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639841 | ||||||
chr6:46639858
|
T | C | 20 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(17): Show | 20 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-190A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639858 | ||||||
chr6:46639943
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-275A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639943 | ||||||
chr6:46639971
|
C | T | 227 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.314-303G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639971 | ||||||
chr6:46639980
|
C | T | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-312G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46639980 | ||||||
chr6:46640055
|
G | A | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG00741.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.314-387C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640055 | ||||||
chr6:46640069
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.314-401G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640069 | ||||||
chr6:46640152
|
G | A | 227 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.314-484C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640152 | ||||||
chr6:46640192
|
G | T | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-524C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640192 | ||||||
chr6:46640735
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.314-1067G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640735 | ||||||
chr6:46640770
|
G | A | 1 | a0004c0005t0001g0020 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.314-1102C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640770 | ||||||
chr6:46640806
|
T | A | 1 | a0002c0002t0001g0174 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.314-1138A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640806 | ||||||
chr6:46640862
|
C | T | 1 | a0003c0003t0001g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.314-1194G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640862 | ||||||
chr6:46640937
|
C | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.313+1226G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46640937 | ||||||
chr6:46641002
|
T | C | 1 | a0002c0002t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+1161A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641002 | ||||||
chr6:46641029
|
G | C | 227 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.313+1134C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641029 | ||||||
chr6:46641221
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+942G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641221 | ||||||
chr6:46641346
|
A | T | 4 | a0002c0002t0002g0133a0002c0002t0002g0300a0002c0002t0002g0301others(1): Show | 4 | HG02896.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+817T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641346 | ||||||
chr6:46641347
|
A | T | 4 | a0002c0002t0002g0133a0002c0002t0002g0300a0002c0002t0002g0301others(1): Show | 4 | HG02896.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+816T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641347 | ||||||
chr6:46641594
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.313+569A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641594 | ||||||
chr6:46641833
|
G | A | 5 | a0003c0003t0002g0257a0003c0003t0002g0272a0005c0004t0001g0237others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+330C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641833 | ||||||
chr6:46641939
|
T | C | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.313+224A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46641939 | ||||||
chr6:46642047
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313+116A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 2/11 | chr6 | 46642047 | ||||||
chr6:46642361
|
T | A | 5 | a0005c0004t0001g0284a0005c0004t0001g0287a0005c0004t0001g0288others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-63A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642361 | ||||||
chr6:46642450
|
G | C | 1 | a0002c0002t0002g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178-152C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642450 | ||||||
chr6:46642608
|
T | C | 1 | a0005c0004t0001g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-310A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642608 | ||||||
chr6:46642757
|
G | C | 1 | a0006c0006t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-459C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642757 | ||||||
chr6:46642779
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0003g0075 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.178-481T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642779 | ||||||
chr6:46642952
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.178-654G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46642952 | ||||||
chr6:46643274
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0177 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.178-976G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643274 | ||||||
chr6:46643807
|
TTTG | T | 13 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(10): Show | 13 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-1512_178-1510d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643807 | ||||||
chr6:46643850
|
G | A | 6 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(3): Show | 6 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1552C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46643850 | ||||||
chr6:46644028
|
T | C | 48 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0092others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.178-1730A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644028 | ||||||
chr6:46644112
|
T | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0002c0002t0002g0236others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-1814A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644112 | ||||||
chr6:46644166
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-1868G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644166 | ||||||
chr6:46644233
|
T | C | 1 | a0002c0002t0001g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.178-1935A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644233 | ||||||
chr6:46644398
|
A | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0002c0002t0002g0236others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-2100T>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644398 | ||||||
chr6:46644432
|
C | G | 1 | a0002c0002t0002g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.178-2134G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644432 | ||||||
chr6:46644629
|
T | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(6): Show | 9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.178-2331A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644629 | ||||||
chr6:46644910
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-2612C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644910 | ||||||
chr6:46644916
|
C | T | 303 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(300): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.178-2618G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46644916 | ||||||
chr6:46645261
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.178-2963A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645261 | ||||||
chr6:46645317
|
A | G | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3019T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645317 | ||||||
chr6:46645346
|
T | C | 203 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(200): Show | 204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.178-3048A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645346 | ||||||
chr6:46645617
|
A | G | 1 | a0002c0002t0002g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.178-3319T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645617 | ||||||
chr6:46645795
|
C | A | 1 | a0003c0003t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178-3497G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645795 | ||||||
chr6:46645977
|
A | T | 2 | a0001c0001t0002g0238a0001c0001t0005g0273 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.178-3679T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46645977 | ||||||
chr6:46646089
|
C | T | 1 | a0004c0005t0001g0017 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.178-3791G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646089 | ||||||
chr6:46646255
|
T | G | 1 | a0008c0008t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.178-3957A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646255 | ||||||
chr6:46646322
|
A | T | 13 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(10): Show | 13 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-4024T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646322 | ||||||
chr6:46646702
|
T | G | 45 | a0003c0003t0001g0048a0003c0003t0001g0226a0003c0003t0001g0259others(42): Show | 45 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.178-4404A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646702 | ||||||
chr6:46646793
|
G | A | 1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.178-4495C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46646793 | ||||||
chr6:46647093
|
C | G | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-4795G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647093 | ||||||
chr6:46647651
|
T | G | 1 | a0002c0002t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.177+4755A>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647651 | ||||||
chr6:46647675
|
C | T | 1 | a0004c0005t0001g0036 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.177+4731G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647675 | ||||||
chr6:46647947
|
C | G | 3 | a0002c0002t0002g0300a0002c0002t0002g0301a0002c0002t0002g0302 | 3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.177+4459G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46647947 | ||||||
chr6:46648055
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+4351G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648055 | ||||||
chr6:46648506
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0002c0002t0001g0130 | 3 | NA18995.hp1 NA19054.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.177+3900G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648506 | ||||||
chr6:46648524
|
A | AG | 28 | a0001c0001t0001g0050a0001c0001t0001g0121a0001c0001t0001g0239others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.177+3881dupC | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648524 | ||||||
chr6:46648531
|
A | G | 1 | a0004c0005t0001g0010 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.177+3875T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648531 | ||||||
chr6:46648555
|
A | G | 1 | a0002c0002t0002g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.177+3851T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648555 | ||||||
chr6:46648743
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.177+3663C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648743 | ||||||
chr6:46648929
|
A | G | 1 | a0002c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.177+3477T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46648929 | ||||||
chr6:46649094
|
T | C | 7 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG02615.hp1 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+3312A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649094 | ||||||
chr6:46649131
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0177 | 3 | HG01891.hp1 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.177+3275C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649131 | ||||||
chr6:46649206
|
T | A | 1 | a0002c0002t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.177+3200A>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649206 | ||||||
chr6:46649317
|
T | C | 1 | a0002c0002t0002g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.177+3089A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649317 | ||||||
chr6:46649490
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0003g0075 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.177+2916A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649490 | ||||||
chr6:46649581
|
C | G | 108 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.177+2825G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649581 | ||||||
chr6:46649891
|
G | A | 3 | a0002c0002t0001g0253a0002c0002t0001g0266a0002c0002t0002g0252 | 3 | HG00558.hp1 HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.177+2515C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46649891 | ||||||
chr6:46650067
|
C | T | 1 | a0002c0002t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.177+2339G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650067 | ||||||
chr6:46650111
|
T | TAC | 94 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0117others(91): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.177+2293_177+2294d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACAC | 14 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(11): Show | 14 | HG00741.hp1 HG02257.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+2291_177+2294d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACACAC | 4 | a0001c0001t0002g0238a0001c0001t0005g0273a0004c0005t0001g0021others(1): Show | 4 | HG03516.hp1 NA18951.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+2289_177+2294d others(8): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACACACA others(5): Show |
1 | a0003c0003t0002g0221 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.177+2283_177+2294d others(14): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACACACA others(7): Show |
1 | a0003c0003t0002g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.177+2281_177+2294d others(16): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACACACA others(9): Show |
21 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(18): Show | 21 | HG00735.hp2 HG01071.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.177+2279_177+2294d others(18): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
T | TACACACA others(11): Show |
1 | a0003c0003t0001g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.177+2277_177+2294d others(20): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650111
|
TAC | T | 4 | a0001c0001t0001g0179a0001c0001t0007g0049a0002c0002t0002g0118others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+2293_177+2294d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650111 | ||||||
chr6:46650295
|
G | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02738.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.177+2111C>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650295 | ||||||
chr6:46650375
|
C | T | 41 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.177+2031G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650375 | ||||||
chr6:46650383
|
C | CT | 266 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.177+2022dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650383 | ||||||
chr6:46650484
|
C | CT | 35 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0260others(32): Show | 35 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.177+1921dupA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
C | CTT | 40 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0239others(37): Show | 41 | HG00280.hp1 HG00408.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.177+1920_177+1921d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
C | CTTT | 31 | a0001c0001t0001g0096a0001c0001t0001g0227a0001c0001t0001g0228others(28): Show | 31 | HG00609.hp1 HG01175.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.177+1919_177+1921d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
C | CTTTT | 8 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01261.hp1 HG01975.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+1918_177+1921d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
CT | C | 13 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(10): Show | 13 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+1921delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
CTT | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0097a0001c0001t0001g0290others(5): Show | 8 | HG00423.hp1 HG01109.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+1920_177+1921d others(4): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
CTTT | C | 42 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0052others(39): Show | 42 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.177+1919_177+1921d others(5): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
CTTTT | C | 91 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.177+1918_177+1921d others(6): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650484
|
CTTTTT | C | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0085others(8): Show | 11 | HG00140.hp1 HG01192.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+1917_177+1921d others(7): Show |
CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650484 | ||||||
chr6:46650552
|
C | G | 275 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(272): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.177+1854G>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650552 | ||||||
chr6:46650586
|
C | A | 1 | a0002c0002t0002g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177+1820G>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650586 | ||||||
chr6:46650678
|
AT | A | 105 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(102): Show | 105 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.177+1727delA | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650678 | ||||||
chr6:46650716
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.177+1690T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650716 | ||||||
chr6:46650719
|
T | C | 121 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.177+1687A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650719 | ||||||
chr6:46650732
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.177+1674A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46650732 | ||||||
chr6:46651063
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.177+1343T>C | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46651063 | ||||||
chr6:46651739
|
A | T | 103 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(100): Show | 103 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.177+667T>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46651739 | ||||||
chr6:46652194
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | NA18949.hp2 NA18963.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.177+212G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652194 | ||||||
chr6:46652302
|
G | A | 3 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0002g0297 | 3 | NA18945.hp1 NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.177+104C>T | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652302 | ||||||
chr6:46652360
|
G | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.177+46C>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652360 | ||||||
chr6:46652367
|
T | C | 3 | a0002c0002t0002g0300a0002c0002t0002g0301a0002c0002t0002g0302 | 3 | HG02896.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.177+39A>G | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652367 | ||||||
chr6:46652398
|
C | T | 46 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(43): Show | 46 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.177+8G>A | CYP39A1 | ENSG00000146233.8 | transcript | ENST00000275016.3 | protein_coding | 1/11 | chr6 | 46652398 |