geneid | 8453 |
---|---|
ensemblid | ENSG00000108094.17 |
hgncid | 2552 |
symbol | CUL2 |
name | cullin 2 |
refseq_nuc | NM_003591.4 |
refseq_prot | NP_003582.2 |
ensembl_nuc | ENST00000374749.8 |
ensembl_prot | ENSP00000363881.3 |
mane_status | MANE Select |
chr | chr10 |
start | 35008551 |
end | 35090341 |
strand | - |
ver | v1.2 |
region | chr10:35008551-35090341 |
region5000 | chr10:35003551-35095341 |
regionname0 | CUL2_chr10_35008551_35090341 |
regionname5000 | CUL2_chr10_35003551_35095341 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2238 | 176 | 64 | 32 | 57 | 4 | 17 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0002 | 0/0 | 2238 | 71 | 4 | 13 | 42 | 5 | 7 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0003 | 0/0 | 2238 | 35 | 4 | 12 | 6 | 1 | 12 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0004 | 0/0 | 2238 | 12 | 9 | 3 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0005 | 0/0 | 2238 | 3 | 3 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0006 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0007 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
c0008 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1948 | 81 | 25 | 19 | 29 | 4 | 4 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0002 | 0/0 | 1948 | 38 | 1 | 0 | 36 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0003 | 0/0 | 1950 | 26 | 1 | 8 | 13 | 0 | 4 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0004 | 0/0 | 1946 | 25 | 2 | 13 | 0 | 5 | 5 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0005 | 0/0 | 1946 | 21 | 1 | 10 | 6 | 1 | 3 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0006 | 0/0 | 1943 | 12 | 9 | 3 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0007 | 1/0 | 1946 | 12 | 7 | 1 | 1 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0008 | 0/0 | 1950 | 11 | 1 | 0 | 9 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0009 | 0/0 | 1945 | 10 | 10 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0010 | 0/0 | 1948 | 9 | 0 | 0 | 0 | 0 | 9 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0011 | 0/0 | 1947 | 6 | 2 | 1 | 1 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0012 | 0/0 | 1948 | 6 | 6 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0013 | 0/1 | 1948 | 5 | 0 | 0 | 0 | 0 | 4 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0014 | 0/0 | 1947 | 4 | 0 | 0 | 4 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0015 | 0/0 | 1950 | 4 | 3 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0016 | 0/0 | 1952 | 3 | 2 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0017 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0018 | 0/0 | 1946 | 2 | 1 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0019 | 0/0 | 1949 | 2 | 2 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0020 | 0/0 | 1947 | 2 | 1 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0021 | 0/0 | 1945 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0022 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0023 | 0/0 | 1951 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0024 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0025 | 0/0 | 1934 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0026 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0027 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0028 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0029 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0030 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0031 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0032 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0033 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0034 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0035 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0036 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0037 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0038 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
t0039 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2238 | 176 | 64 | 32 | 57 | 4 | 17 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002 | 0/0 | 2238 | 71 | 4 | 13 | 42 | 5 | 7 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003 | 0/0 | 2238 | 35 | 4 | 12 | 6 | 1 | 12 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0004 | 0/0 | 2238 | 12 | 9 | 3 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0005 | 0/0 | 2238 | 3 | 3 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0006 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0008 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0002c0007 | 0/0 | 2238 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4185 | 78 | 22 | 19 | 29 | 4 | 4 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0003 | 0/0 | 4187 | 25 | 1 | 8 | 13 | 0 | 3 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0007 | 1/0 | 4183 | 12 | 7 | 1 | 1 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0008 | 0/0 | 4187 | 11 | 1 | 0 | 9 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0009 | 0/0 | 4182 | 10 | 10 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0011 | 0/0 | 4184 | 6 | 2 | 1 | 1 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0012 | 0/0 | 4185 | 6 | 6 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0013 | 0/1 | 4185 | 5 | 0 | 0 | 0 | 0 | 4 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0015 | 0/0 | 4187 | 2 | 1 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0016 | 0/0 | 4189 | 3 | 2 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0018 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0019 | 0/0 | 4186 | 2 | 2 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0022 | 0/0 | 4184 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0023 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0024 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0025 | 0/0 | 4171 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0026 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0027 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0030 | 0/0 | 4181 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0031 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0032 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0034 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0035 | 0/0 | 4186 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0036 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0037 | 0/0 | 4185 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0038 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0001t0039 | 0/0 | 4187 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0002 | 0/0 | 4185 | 38 | 1 | 0 | 36 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0004 | 0/0 | 4183 | 25 | 2 | 13 | 0 | 5 | 5 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0014 | 0/0 | 4184 | 4 | 0 | 0 | 4 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0017 | 0/0 | 4183 | 2 | 0 | 0 | 2 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0021 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0002t0029 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003t0005 | 0/0 | 4183 | 21 | 1 | 10 | 6 | 1 | 3 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003t0010 | 0/0 | 4185 | 9 | 0 | 0 | 0 | 0 | 9 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003t0015 | 0/0 | 4187 | 2 | 2 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003t0020 | 0/0 | 4184 | 2 | 1 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0003t0028 | 0/0 | 4183 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0004t0006 | 0/0 | 4180 | 12 | 9 | 3 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0005t0001 | 0/0 | 4185 | 3 | 3 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0006t0003 | 0/0 | 4187 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0001c0008t0033 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
a0002c0007t0018 | 0/0 | 4183 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | copy fasta | chr10 | 35003551 | 35095341 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0011g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0013g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0013g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0013g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0013g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0015g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0016g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0022g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0023g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0024g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0025g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0026g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0027g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0030g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0031g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0032g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0034g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0035g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0036g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0037g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0038g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0001t0039g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0014g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0017g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0017g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0021g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0002t0029g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0010g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0015g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0020g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0020g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0003t0028g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0004t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0005t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0006t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0001c0008t0033g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
a0002c0007t0018g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0004 | g0172 | EUR | FIN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0139 | EUR | FIN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00544 | hp2 | a0001 | c0001 | t0008 | g0094 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00621 | hp2 | a0001 | c0001 | t0008 | g0087 | EAS | CHS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0143 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00639 | hp2 | a0001 | c0003 | t0005 | g0196 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00642 | hp2 | a0001 | c0001 | t0016 | g0116 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00735 | hp1 | a0001 | c0003 | t0005 | g0199 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00738 | hp2 | a0001 | c0004 | t0006 | g0244 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00741 | hp1 | a0001 | c0001 | t0015 | g0012 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0291 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01069 | hp1 | a0001 | c0002 | t0004 | g0137 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01069 | hp2 | a0001 | c0001 | t0022 | g0250 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01071 | hp1 | a0001 | c0004 | t0006 | g0290 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01074 | hp1 | a0001 | c0003 | t0005 | g0194 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0254 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0167 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01081 | hp2 | a0001 | c0003 | t0005 | g0198 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01099 | hp1 | a0001 | c0003 | t0020 | g0177 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01109 | hp2 | a0001 | c0004 | t0006 | g0287 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01167 | hp1 | a0001 | c0003 | t0005 | g0192 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01168 | hp2 | a0001 | c0002 | t0004 | g0127 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01169 | hp1 | a0001 | c0003 | t0005 | g0193 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01175 | hp1 | a0001 | c0002 | t0004 | g0179 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0246 | AMR | PUR | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0144 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01358 | hp1 | a0001 | c0002 | t0004 | g0135 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01433 | hp1 | a0001 | c0003 | t0005 | g0197 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01433 | hp2 | a0001 | c0003 | t0028 | g0211 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01515 | hp1 | a0001 | c0003 | t0005 | g0207 | EUR | IBS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01515 | hp2 | a0001 | c0002 | t0004 | g0136 | EUR | IBS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0173 | EUR | IBS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0280 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0232 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01928 | hp2 | a0001 | c0002 | t0004 | g0141 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01975 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01981 | hp1 | a0001 | c0003 | t0005 | g0203 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01993 | hp2 | a0001 | c0002 | t0004 | g0129 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02040 | hp1 | a0001 | c0002 | t0017 | g0126 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02040 | hp2 | a0001 | c0002 | t0017 | g0162 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02074 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | KHV | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0234 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02257 | hp1 | a0001 | c0004 | t0006 | g0243 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0237 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0238 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02280 | hp1 | a0001 | c0003 | t0015 | g0214 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0128 | AMR | PEL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02572 | hp1 | a0001 | c0004 | t0006 | g0289 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02602 | hp1 | a0002 | c0007 | t0018 | g0053 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02602 | hp2 | a0001 | c0002 | t0004 | g0130 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02615 | hp1 | a0001 | c0004 | t0006 | g0271 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02622 | hp1 | a0001 | c0001 | t0027 | g0248 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02630 | hp2 | a0001 | c0001 | t0036 | g0295 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02647 | hp1 | a0001 | c0001 | t0015 | g0255 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02647 | hp2 | a0001 | c0004 | t0006 | g0242 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02683 | hp1 | a0001 | c0003 | t0005 | g0208 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02717 | hp2 | a0001 | c0001 | t0016 | g0081 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02723 | hp1 | a0001 | c0004 | t0006 | g0286 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02723 | hp2 | a0001 | c0001 | t0026 | g0247 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02735 | hp2 | a0001 | c0001 | t0013 | g0265 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0168 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02809 | hp2 | a0001 | c0004 | t0006 | g0245 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0229 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02886 | hp1 | a0001 | c0003 | t0005 | g0217 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0278 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02895 | hp2 | a0001 | c0001 | t0032 | g0288 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0230 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0277 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0279 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0276 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0233 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0281 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0221 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02965 | hp2 | a0001 | c0004 | t0006 | g0284 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03017 | hp1 | a0001 | c0003 | t0005 | g0206 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0125 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0282 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03130 | hp1 | a0001 | c0001 | t0016 | g0055 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03195 | hp2 | a0001 | c0001 | t0038 | g0292 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03225 | hp1 | a0001 | c0003 | t0015 | g0213 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03225 | hp2 | a0001 | c0001 | t0037 | g0293 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03239 | hp2 | a0001 | c0003 | t0005 | g0195 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0239 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03486 | hp1 | a0001 | c0001 | t0019 | g0216 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03486 | hp2 | a0001 | c0001 | t0034 | g0259 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03491 | hp1 | a0001 | c0003 | t0010 | g0004 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03491 | hp2 | a0001 | c0001 | t0035 | g0018 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03492 | hp1 | a0001 | c0003 | t0010 | g0004 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03516 | hp2 | a0001 | c0001 | t0039 | g0294 | AFR | ESN | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | GWD | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03579 | hp2 | a0001 | c0003 | t0020 | g0176 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03669 | hp1 | a0001 | c0001 | t0013 | g0264 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03669 | hp2 | a0001 | c0003 | t0010 | g0190 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03688 | hp1 | a0001 | c0001 | t0013 | g0266 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03688 | hp2 | a0001 | c0003 | t0010 | g0189 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03704 | hp1 | a0001 | c0003 | t0010 | g0212 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03704 | hp2 | a0001 | c0002 | t0021 | g0132 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0133 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03710 | hp2 | a0001 | c0003 | t0010 | g0187 | SAS | PJL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0235 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0080 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03834 | hp1 | a0001 | c0006 | t0003 | g0021 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03834 | hp2 | a0001 | c0001 | t0011 | g0241 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0156 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03927 | hp2 | a0001 | c0001 | t0013 | g0274 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0069 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03942 | hp2 | a0001 | c0003 | t0010 | g0188 | SAS | BEB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04115 | hp1 | a0001 | c0003 | t0010 | g0191 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0138 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04199 | hp1 | a0001 | c0002 | t0004 | g0131 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0120 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG04204 | hp2 | a0001 | c0003 | t0010 | g0186 | SAS | STU | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18906 | hp2 | a0001 | c0001 | t0031 | g0014 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18943 | hp1 | a0001 | c0001 | t0008 | g0061 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18954 | hp1 | a0001 | c0001 | t0025 | g0077 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18959 | hp1 | a0001 | c0002 | t0014 | g0158 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18959 | hp2 | a0001 | c0003 | t0005 | g0205 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18965 | hp1 | a0001 | c0002 | t0014 | g0180 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18965 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18967 | hp1 | a0001 | c0001 | t0030 | g0023 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18975 | hp1 | a0001 | c0003 | t0005 | g0209 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18980 | hp2 | a0001 | c0003 | t0005 | g0200 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18984 | hp1 | a0001 | c0003 | t0005 | g0202 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18985 | hp1 | a0001 | c0003 | t0005 | g0204 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18990 | hp1 | a0001 | c0003 | t0005 | g0210 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18994 | hp1 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19004 | hp2 | a0001 | c0001 | t0024 | g0082 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19007 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19010 | hp1 | a0001 | c0008 | t0033 | g0106 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19012 | hp1 | a0001 | c0001 | t0023 | g0104 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0224 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0227 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19057 | hp2 | a0001 | c0002 | t0014 | g0169 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19083 | hp2 | a0001 | c0002 | t0014 | g0149 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19240 | hp1 | a0001 | c0004 | t0006 | g0006 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | YRI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ASW | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0223 | AFR | ASW | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA20805 | hp2 | a0001 | c0002 | t0004 | g0123 | EUR | TSI | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG01123 | hp2 | a0001 | c0003 | t0005 | g0201 | AMR | CLM | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02486 | hp2 | a0001 | c0002 | t0029 | g0134 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0283 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0215 | AFR | ACB | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03471 | hp1 | a0001 | c0004 | t0006 | g0285 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0231 | AFR | MSL | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG06807 | hp1 | a0001 | c0002 | t0004 | g0142 | AFR | USA | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0236 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
NA21309 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | LWK | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0268 | REF | REF | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0226 | REF | REF | CUL2_chr10_35003551_35095341 | CUL2 | chr10 | 35003551 | 35095341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35035215
|
T | C | 1 | a0002 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.959A>G | p.His320Arg | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/21 | 1144/4183 | 959/2238 | 320/745 | chr10 | 35035215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35013777
|
C | T | 2 | a0001c0002a0001c0003 | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
synonymous_variant | LOW | c.1911G>A | p.Ser637Ser | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/21 | 2096/4183 | 1911/2238 | 637/745 | chr10 | 35013777 | ||
chr10:35028819
|
A | G | 1 | a0001c0006 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1608T>C | p.Ser536Ser | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/21 | 1793/4183 | 1608/2238 | 536/745 | chr10 | 35028819 | ||
chr10:35032486
|
C | T | 1 | a0001c0002 | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
synonymous_variant | LOW | c.1119G>A | p.Thr373Thr | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 12/21 | 1304/4183 | 1119/2238 | 373/745 | chr10 | 35032486 | ||
chr10:35049745
|
C | T | 1 | a0001c0004 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
synonymous_variant | LOW | c.444G>A | p.Arg148Arg | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/21 | 629/4183 | 444/2238 | 148/745 | chr10 | 35049745 | ||
chr10:35063050
|
A | G | 1 | a0001c0005 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.132T>C | p.Ala44Ala | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/21 | 317/4183 | 132/2238 | 44/745 | chr10 | 35063050 | ||
chr10:35071249
|
G | A | 1 | a0001c0008 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.69C>T | p.Ala23Ala | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/21 | 254/4183 | 69/2238 | 23/745 | chr10 | 35071249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35008599
|
T | G | 1 | a0001c0004t0006 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1712A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1712 | chr10 | 35008599 | |||||
chr10:35008755
|
A | G | 7 | a0001c0002t0002a0001c0002t0004a0001c0002t0014others(4): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1556T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1556 | chr10 | 35008755 | |||||
chr10:35008892
|
T | C | 3 | a0001c0001t0008a0001c0001t0018a0002c0007t0018 | 13 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1419A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1419 | chr10 | 35008892 | |||||
chr10:35009055
|
G | A | 3 | a0001c0003t0005a0001c0003t0010a0001c0003t0028 | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1256C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1256 | chr10 | 35009055 | |||||
chr10:35009108
|
G | A | 1 | a0001c0001t0031 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1203C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1203 | chr10 | 35009108 | |||||
chr10:35009183
|
G | GAT | 3 | a0001c0001t0037a0001c0002t0002a0001c0002t0014 | 43 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1127dupAT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1127 | chr10 | 35009183 | |||||
chr10:35009190
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0025 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110_*1120delATAT others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1110 | chr10 | 35009190 | |||||
chr10:35009201
|
T | A | 1 | a0001c0001t0034 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1110A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1110 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TATATTA | 3 | a0001c0001t0032a0001c0001t0036a0001c0001t0038 | 3 | HG02630.hp2 HG02895.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1109_*1110insTAAT others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TATTA | 3 | a0001c0001t0015a0001c0001t0039a0001c0003t0015 | 5 | HG00741.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1109_*1110insTAAT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TATTATA | 2 | a0001c0001t0016a0001c0001t0023 | 4 | HG00642.hp2 HG02717.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1109_*1110insTATA others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TTA | 7 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(4): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1108_*1109dupTA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TTATA | 4 | a0001c0001t0003a0001c0001t0008a0001c0001t0024others(1): Show | 38 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1106_*1109dupTATA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
T | TTATATAT others(22): Show |
1 | a0001c0008t0033 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109_*1110insTATA others(25): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009201 | |||||
chr10:35009201
|
TTA | T | 3 | a0001c0001t0030a0001c0002t0029a0001c0004t0006 | 14 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1108_*1109delTA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1108 | chr10 | 35009201 | |||||
chr10:35009202
|
T | A | 2 | a0001c0002t0017a0001c0003t0028 | 3 | HG01433.hp2 HG02040.hp1 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1109A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1109 | chr10 | 35009202 | |||||
chr10:35009203
|
A | T | 2 | a0001c0002t0017a0001c0003t0028 | 3 | HG01433.hp2 HG02040.hp1 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1108T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 1108 | chr10 | 35009203 | |||||
chr10:35009486
|
T | C | 1 | a0001c0001t0027 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*825A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 825 | chr10 | 35009486 | |||||
chr10:35009513
|
T | TG | 5 | a0001c0001t0011a0001c0001t0012a0001c0001t0019others(2): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*797dupC | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 797 | chr10 | 35009513 | |||||
chr10:35009991
|
T | TA | 3 | a0001c0001t0012a0001c0001t0035a0001c0003t0020 | 9 | HG01099.hp1 HG01891.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*319dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 319 | chr10 | 35009991 | |||||
chr10:35009991
|
TA | T | 10 | a0001c0001t0009a0001c0001t0022a0001c0001t0023others(7): Show | 33 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*319delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 319 | chr10 | 35009991 | |||||
chr10:35010157
|
C | T | 1 | a0001c0001t0013 | 5 | HG02735.hp2 HG03669.hp1 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 154 | chr10 | 35010157 | |||||
chr10:35010293
|
C | T | 1 | a0001c0001t0036 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 21/21 | 18 | chr10 | 35010293 | |||||
chr10:35090286
|
G | A | 4 | a0001c0001t0036a0001c0001t0037a0001c0001t0038others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-130C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/21 | chr10 | 35090286 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:35010575
|
G | C | 1 | a0001c0001t0016g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2107-133C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35010575 | ||||||
chr10:35010653
|
T | C | 1 | a0001c0001t0031g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2107-211A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35010653 | ||||||
chr10:35010741
|
G | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2107-299C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35010741 | ||||||
chr10:35010787
|
G | C | 104 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(101): Show | 108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2107-345C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35010787 | ||||||
chr10:35010787
|
G | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2107-345C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35010787 | ||||||
chr10:35011084
|
T | C | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2107-642A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011084 | ||||||
chr10:35011203
|
ATTTTTTA others(8): Show |
A | 12 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(9): Show | 12 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+630_2106+644d others(17): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011203 | ||||||
chr10:35011206
|
T | G | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2106+642A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011206 | ||||||
chr10:35011211
|
ATTTTTTT | A | 102 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0026g0247others(99): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2106+630_2106+636d others(9): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011211 | ||||||
chr10:35011233
|
A | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.2106+615T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011233 | ||||||
chr10:35011490
|
C | T | 1 | a0001c0001t0003g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2106+358G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011490 | ||||||
chr10:35011695
|
G | A | 129 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2106+153C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011695 | ||||||
chr10:35011701
|
G | A | 12 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(9): Show | 12 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+147C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011701 | ||||||
chr10:35011717
|
G | T | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2106+131C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011717 | ||||||
chr10:35011790
|
T | A | 3 | a0001c0004t0006g0006a0001c0004t0006g0289a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2106+58A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 20/20 | chr10 | 35011790 | ||||||
chr10:35012053
|
CT | C | 14 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0002t0002g0148others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1990-90delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012053 | ||||||
chr10:35012119
|
T | C | 1 | a0001c0001t0031g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1990-155A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012119 | ||||||
chr10:35012153
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1990-189T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012153 | ||||||
chr10:35012212
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1990-248A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012212 | ||||||
chr10:35012232
|
T | C | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1990-268A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012232 | ||||||
chr10:35012259
|
C | T | 2 | a0001c0003t0005g0192a0001c0003t0005g0193 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1990-295G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012259 | ||||||
chr10:35012618
|
G | C | 1 | a0001c0003t0005g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1990-654C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012618 | ||||||
chr10:35012667
|
A | G | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1990-703T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012667 | ||||||
chr10:35012677
|
A | C | 1 | a0001c0002t0002g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1990-713T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012677 | ||||||
chr10:35012693
|
C | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1990-729G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012693 | ||||||
chr10:35012719
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1990-755C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012719 | ||||||
chr10:35012794
|
G | C | 1 | a0001c0003t0028g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1990-830C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35012794 | ||||||
chr10:35013126
|
G | A | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1989+573C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013126 | ||||||
chr10:35013303
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1989+396G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013303 | ||||||
chr10:35013344
|
C | CA | 8 | a0001c0001t0001g0050a0001c0001t0001g0090a0001c0002t0004g0141others(5): Show | 8 | HG01928.hp2 HG02280.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1989+354dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013344 | ||||||
chr10:35013344
|
C | CAAA | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1989+352_1989+354d others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013344 | ||||||
chr10:35013388
|
AC | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+310delG | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013388 | ||||||
chr10:35013448
|
T | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1989+251A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013448 | ||||||
chr10:35013500
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1989+199A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013500 | ||||||
chr10:35013619
|
C | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1989+80G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013619 | ||||||
chr10:35013628
|
T | C | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1989+71A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 19/20 | chr10 | 35013628 | ||||||
chr10:35013824
|
A | G | 1 | a0001c0002t0002g0147 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1888-24T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35013824 | ||||||
chr10:35014058
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1888-258A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014058 | ||||||
chr10:35014073
|
A | G | 1 | a0001c0001t0013g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1888-273T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014073 | ||||||
chr10:35014089
|
A | G | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1888-289T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014089 | ||||||
chr10:35014401
|
C | T | 1 | a0001c0001t0009g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1888-601G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014401 | ||||||
chr10:35014406
|
G | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1888-606C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014406 | ||||||
chr10:35014430
|
A | G | 1 | a0001c0001t0003g0258 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1888-630T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014430 | ||||||
chr10:35014671
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1888-871T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014671 | ||||||
chr10:35014756
|
C | T | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1888-956G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014756 | ||||||
chr10:35014770
|
T | C | 1 | a0001c0003t0010g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1888-970A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014770 | ||||||
chr10:35014914
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1888-1114A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35014914 | ||||||
chr10:35015014
|
C | G | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1887+1178G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015014 | ||||||
chr10:35015250
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1887+942C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015250 | ||||||
chr10:35015293
|
C | CA | 12 | a0001c0001t0001g0031a0001c0001t0001g0098a0001c0001t0001g0261others(9): Show | 12 | HG01884.hp1 HG02129.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1887+898dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015293 | ||||||
chr10:35015293
|
CA | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1887+898delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015293 | ||||||
chr10:35015404
|
G | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887+788C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015404 | ||||||
chr10:35015449
|
A | G | 2 | a0001c0003t0005g0201a0001c0003t0005g0203 | 2 | HG01123.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1887+743T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015449 | ||||||
chr10:35015471
|
A | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA19002.hp1 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1887+721T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015471 | ||||||
chr10:35015934
|
T | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1887+258A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015934 | ||||||
chr10:35015980
|
A | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1887+212T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35015980 | ||||||
chr10:35016043
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1887+149C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 18/20 | chr10 | 35016043 | ||||||
chr10:35016673
|
T | C | 2 | a0001c0001t0003g0020a0001c0006t0003g0021 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1685-279A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016673 | ||||||
chr10:35016817
|
C | A | 2 | a0001c0001t0003g0020a0001c0006t0003g0021 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1685-423G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016817 | ||||||
chr10:35016926
|
C | CA | 13 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0003g0052others(10): Show | 13 | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1685-533dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016926 | ||||||
chr10:35016926
|
CA | C | 6 | a0001c0001t0001g0059a0001c0001t0007g0227a0001c0002t0002g0146others(3): Show | 6 | HG02015.hp2 NA18961.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685-533delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016926 | ||||||
chr10:35016943
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1685-549G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016943 | ||||||
chr10:35016944
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1685-550T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35016944 | ||||||
chr10:35017061
|
C | G | 118 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(115): Show | 123 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1685-667G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017061 | ||||||
chr10:35017278
|
C | T | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1685-884G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017278 | ||||||
chr10:35017282
|
C | T | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-888G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017282 | ||||||
chr10:35017309
|
T | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685-915A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017309 | ||||||
chr10:35017338
|
AATGTTTA others(54): Show |
A | 1 | a0001c0001t0012g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1685-1005_1685-945 others(64): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017338 | ||||||
chr10:35017387
|
T | C | 1 | a0001c0003t0010g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1685-993A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017387 | ||||||
chr10:35017576
|
C | T | 9 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(6): Show | 9 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1685-1182G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017576 | ||||||
chr10:35017648
|
A | G | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1685-1254T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017648 | ||||||
chr10:35017692
|
CA | C | 139 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0033others(136): Show | 144 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1685-1299delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017692 | ||||||
chr10:35017745
|
T | C | 1 | a0001c0002t0017g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1685-1351A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017745 | ||||||
chr10:35017857
|
T | A | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1685-1463A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017857 | ||||||
chr10:35017872
|
GT | G | 97 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(94): Show | 102 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1685-1479delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017872 | ||||||
chr10:35017874
|
TTA | T | 5 | a0001c0002t0002g0147a0001c0002t0002g0175a0001c0002t0014g0180others(2): Show | 5 | HG01515.hp1 HG02040.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-1482_1685-148 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017874 | ||||||
chr10:35017875
|
T | A | 16 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(13): Show | 16 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1685-1481A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017875 | ||||||
chr10:35017931
|
G | A | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1685-1537C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017931 | ||||||
chr10:35017935
|
G | C | 1 | a0001c0003t0005g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1685-1541C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35017935 | ||||||
chr10:35018016
|
C | T | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1685-1622G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018016 | ||||||
chr10:35018066
|
G | A | 1 | a0001c0003t0015g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1685-1672C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018066 | ||||||
chr10:35018122
|
C | CA | 139 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(136): Show | 140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1685-1729dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018122 | ||||||
chr10:35018122
|
C | CAA | 54 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0113others(51): Show | 54 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1685-1730_1685-172 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018122 | ||||||
chr10:35018147
|
C | T | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1685-1753G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018147 | ||||||
chr10:35018148
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1685-1754C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018148 | ||||||
chr10:35018156
|
G | A | 3 | a0001c0001t0012g0238a0001c0001t0012g0239a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1685-1762C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018156 | ||||||
chr10:35018241
|
C | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1685-1847G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018241 | ||||||
chr10:35018288
|
C | CA | 6 | a0001c0001t0007g0280a0001c0001t0007g0283a0001c0001t0009g0223others(3): Show | 6 | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685-1895dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018288 | ||||||
chr10:35018288
|
CA | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 147 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1685-1895delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018288 | ||||||
chr10:35018288
|
CAA | C | 51 | a0001c0001t0001g0044a0001c0001t0001g0100a0001c0001t0019g0216others(48): Show | 53 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1685-1896_1685-189 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018288 | ||||||
chr10:35018288
|
CAAA | C | 33 | a0001c0001t0019g0215a0001c0003t0005g0192a0001c0003t0005g0193others(30): Show | 34 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1685-1897_1685-189 others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018288 | ||||||
chr10:35018298
|
A | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1685-1904T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018298 | ||||||
chr10:35018303
|
A | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1685-1909T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018303 | ||||||
chr10:35018589
|
C | A | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1685-2195G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018589 | ||||||
chr10:35018593
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1685-2199C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018593 | ||||||
chr10:35018709
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG01934.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1685-2315C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018709 | ||||||
chr10:35018710
|
C | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG01934.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1685-2316G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018710 | ||||||
chr10:35018750
|
C | T | 1 | a0001c0001t0009g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1685-2356G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018750 | ||||||
chr10:35018763
|
C | CA | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(177): Show | 180 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.1685-2370dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018763 | ||||||
chr10:35018763
|
C | CAA | 102 | a0001c0001t0001g0050a0001c0001t0001g0090a0001c0001t0009g0223others(99): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1685-2371_1685-237 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018763 | ||||||
chr10:35018866
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1685-2472G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35018866 | ||||||
chr10:35019107
|
T | C | 1 | a0001c0002t0004g0129 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1685-2713A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019107 | ||||||
chr10:35019137
|
G | A | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1685-2743C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019137 | ||||||
chr10:35019231
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1685-2837A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019231 | ||||||
chr10:35019239
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0013 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1685-2845G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019239 | ||||||
chr10:35019312
|
T | C | 1 | a0001c0003t0015g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1685-2918A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019312 | ||||||
chr10:35019697
|
G | A | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685-3303C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019697 | ||||||
chr10:35019992
|
A | G | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1685-3598T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35019992 | ||||||
chr10:35020084
|
C | A | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1685-3690G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020084 | ||||||
chr10:35020166
|
TA | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0051others(80): Show | 87 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1685-3773delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020166 | ||||||
chr10:35020177
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1685-3783T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020177 | ||||||
chr10:35020239
|
T | C | 1 | a0001c0003t0010g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1685-3845A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020239 | ||||||
chr10:35020260
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1685-3866C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020260 | ||||||
chr10:35020401
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG01934.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1685-4007G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020401 | ||||||
chr10:35020439
|
G | A | 118 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(115): Show | 123 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1685-4045C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020439 | ||||||
chr10:35020585
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1685-4191A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020585 | ||||||
chr10:35020661
|
A | G | 139 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(136): Show | 144 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1685-4267T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020661 | ||||||
chr10:35020963
|
G | GT | 15 | a0001c0001t0001g0074a0001c0001t0001g0117a0001c0001t0001g0261others(12): Show | 15 | HG01515.hp2 HG02004.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1684+4168dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020963 | ||||||
chr10:35020963
|
GT | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0037others(50): Show | 53 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1684+4168delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35020963 | ||||||
chr10:35021139
|
T | C | 1 | a0001c0001t0009g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1684+3993A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021139 | ||||||
chr10:35021236
|
A | G | 1 | a0001c0003t0015g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1684+3896T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021236 | ||||||
chr10:35021262
|
CT | C | 100 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(97): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1684+3869delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021262 | ||||||
chr10:35021326
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1684+3806C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021326 | ||||||
chr10:35021407
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1684+3725T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021407 | ||||||
chr10:35021442
|
T | C | 2 | a0001c0001t0007g0227a0001c0001t0036g0295 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1684+3690A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021442 | ||||||
chr10:35021442
|
T | TAC | 6 | a0001c0002t0002g0146a0001c0002t0002g0147a0001c0002t0002g0165others(3): Show | 6 | HG02015.hp2 HG02280.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684+3688_1684+368 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021442 | ||||||
chr10:35021442
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1684+3678_1684+368 others(16): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021442 | ||||||
chr10:35021456
|
TACATACA others(7): Show |
T | 14 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(11): Show | 14 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1684+3662_1684+367 others(18): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021456 | ||||||
chr10:35021460
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1684+3672A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021460 | ||||||
chr10:35021470
|
C | T | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1684+3662G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021470 | ||||||
chr10:35021495
|
AGAT | A | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.1684+3634_1684+363 others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021495 | ||||||
chr10:35021528
|
TTAA | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1684+3601_1684+360 others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021528 | ||||||
chr10:35021545
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1684+3587C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021545 | ||||||
chr10:35021556
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0102 | 3 | HG02145.hp1 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1684+3576A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021556 | ||||||
chr10:35021568
|
A | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG00323.hp1 HG00733.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+3564T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021568 | ||||||
chr10:35021752
|
AATGTGGG others(5): Show |
A | 1 | a0001c0003t0005g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1684+3368_1684+337 others(16): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021752 | ||||||
chr10:35021769
|
C | T | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1684+3363G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021769 | ||||||
chr10:35021790
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1684+3342C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021790 | ||||||
chr10:35021821
|
T | TGAGGTGA others(8): Show |
10 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(7): Show | 10 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684+3310_1684+331 others(19): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021821 | ||||||
chr10:35021831
|
C | CGAGGCGA others(3): Show |
5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684+3300_1684+330 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021831 | ||||||
chr10:35021831
|
C | CGAGGT | 11 | a0001c0001t0001g0031a0001c0001t0009g0222a0001c0001t0009g0224others(8): Show | 11 | HG01071.hp1 HG02135.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1684+3296_1684+330 others(9): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021831 | ||||||
chr10:35021831
|
CGAGGT | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684+3296_1684+330 others(9): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021831 | ||||||
chr10:35021831
|
CGAGGTGA others(3): Show |
C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+3291_1684+330 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021831 | ||||||
chr10:35021841
|
T | C | 1 | a0001c0001t0012g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1684+3291A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021841 | ||||||
chr10:35021858
|
A | AGGTGAGG others(8): Show |
80 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(77): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1684+3273_1684+327 others(19): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021858
|
A | AGGTGAGG others(18): Show |
13 | a0001c0003t0005g0194a0001c0003t0005g0195a0001c0003t0005g0196others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1684+3273_1684+327 others(29): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021858
|
A | AGGTGAGG others(28): Show |
3 | a0001c0003t0005g0197a0001c0003t0005g0207a0001c0003t0028g0211 | 3 | HG01433.hp1 HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1684+3273_1684+327 others(39): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021858
|
A | AGGTGAGG others(38): Show |
2 | a0001c0003t0005g0209a0001c0003t0005g0210 | 2 | NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1684+3273_1684+327 others(49): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021858
|
A | AGGTGGGG others(3): Show |
1 | a0001c0001t0009g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1684+3264_1684+327 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021858
|
A | G | 1 | a0001c0004t0006g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1684+3274T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021858 | ||||||
chr10:35021863
|
G | A | 100 | a0001c0001t0012g0233a0001c0002t0002g0001a0001c0002t0002g0003others(97): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1684+3269C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021863 | ||||||
chr10:35021863
|
G | GGGTGGGG others(3): Show |
9 | a0001c0001t0001g0088a0001c0001t0011g0246a0001c0001t0019g0215others(6): Show | 9 | HG01109.hp2 HG01192.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1684+3259_1684+326 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021863 | ||||||
chr10:35021863
|
G | GGGTGGGG others(23): Show |
3 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0271 | 3 | HG00738.hp2 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1684+3239_1684+326 others(34): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021863 | ||||||
chr10:35021863
|
GGGTGGGG others(3): Show |
G | 9 | a0001c0001t0003g0052a0001c0001t0003g0084a0001c0001t0003g0085others(6): Show | 9 | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1684+3259_1684+326 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021863 | ||||||
chr10:35021868
|
G | A | 1 | a0001c0001t0012g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1684+3264C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021868 | ||||||
chr10:35021873
|
A | G | 2 | a0001c0001t0012g0233a0001c0001t0038g0292 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1684+3259T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021873 | ||||||
chr10:35021911
|
C | T | 1 | a0001c0003t0005g0204 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1684+3221G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021911 | ||||||
chr10:35021913
|
A | AGGTGGGG others(3): Show |
1 | a0001c0003t0005g0204 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1684+3218_1684+321 others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021913 | ||||||
chr10:35021914
|
A | G | 100 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(97): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1684+3218T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021914 | ||||||
chr10:35021929
|
C | T | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1684+3203G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021929 | ||||||
chr10:35021966
|
G | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1684+3166C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021966 | ||||||
chr10:35021974
|
C | T | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1684+3158G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35021974 | ||||||
chr10:35022076
|
CGT | C | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1684+3054_1684+305 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022076 | ||||||
chr10:35022079
|
A | T | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1684+3053T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022079 | ||||||
chr10:35022094
|
C | T | 1 | a0001c0003t0005g0195 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1684+3038G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022094 | ||||||
chr10:35022162
|
A | G | 1 | a0001c0001t0011g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1684+2970T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022162 | ||||||
chr10:35022173
|
A | G | 5 | a0001c0002t0002g0148a0001c0002t0002g0155a0001c0002t0002g0174others(2): Show | 5 | HG02040.hp1 HG02135.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684+2959T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022173 | ||||||
chr10:35022441
|
T | A | 1 | a0001c0001t0013g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1684+2691A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022441 | ||||||
chr10:35022513
|
C | T | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+2619G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022513 | ||||||
chr10:35022561
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1684+2571C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022561 | ||||||
chr10:35022686
|
C | CAGTAA | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1684+2441_1684+244 others(9): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35022686 | ||||||
chr10:35023356
|
C | A | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1684+1776G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023356 | ||||||
chr10:35023374
|
G | A | 1 | a0001c0003t0010g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1684+1758C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023374 | ||||||
chr10:35023594
|
GGTT | G | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1684+1535_1684+153 others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023594 | ||||||
chr10:35023601
|
A | C | 1 | a0001c0001t0008g0118 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1684+1531T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023601 | ||||||
chr10:35023758
|
G | GA | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1684+1373_1684+137 others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023758 | ||||||
chr10:35023759
|
G | A | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1684+1373C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35023759 | ||||||
chr10:35024050
|
G | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1684+1082C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024050 | ||||||
chr10:35024067
|
T | C | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1684+1065A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024067 | ||||||
chr10:35024068
|
T | C | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1684+1064A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024068 | ||||||
chr10:35024113
|
G | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0094a0001c0001t0008g0260 | 3 | HG00544.hp2 HG00609.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1684+1019C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024113 | ||||||
chr10:35024518
|
T | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1684+614A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024518 | ||||||
chr10:35024656
|
T | A | 13 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1684+476A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024656 | ||||||
chr10:35024673
|
A | C | 1 | a0001c0001t0036g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1684+459T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024673 | ||||||
chr10:35024728
|
T | C | 1 | a0001c0001t0009g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1684+404A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024728 | ||||||
chr10:35024759
|
C | T | 2 | a0001c0002t0004g0123a0001c0002t0004g0178 | 2 | HG00733.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1684+373G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024759 | ||||||
chr10:35024870
|
G | T | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1684+262C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35024870 | ||||||
chr10:35025018
|
T | C | 1 | a0001c0001t0003g0267 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1684+114A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35025018 | ||||||
chr10:35025055
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1684+77G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35025055 | ||||||
chr10:35025083
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0090 | 3 | HG02056.hp1 NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1684+49T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35025083 | ||||||
chr10:35025091
|
G | C | 1 | a0001c0001t0009g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1684+41C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 17/20 | chr10 | 35025091 | ||||||
chr10:35025202
|
T | TA | 50 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0065others(47): Show | 50 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.1618-5dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35025202 | ||||||
chr10:35025202
|
TA | T | 119 | a0001c0001t0003g0022a0001c0001t0007g0218a0001c0001t0007g0219others(116): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
splice_region_variant&intron_variant | LOW | c.1618-5delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35025202 | ||||||
chr10:35025354
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | NA19002.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1618-156C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35025354 | ||||||
chr10:35026004
|
A | T | 2 | a0001c0001t0018g0046a0002c0007t0018g0053 | 2 | HG02602.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1618-806T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026004 | ||||||
chr10:35026019
|
A | G | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1618-821T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026019 | ||||||
chr10:35026051
|
C | G | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1618-853G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026051 | ||||||
chr10:35026343
|
C | T | 2 | a0001c0003t0020g0176a0001c0003t0020g0177 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1618-1145G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026343 | ||||||
chr10:35026401
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1618-1203G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026401 | ||||||
chr10:35026532
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1618-1334A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026532 | ||||||
chr10:35026567
|
G | T | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-1369C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35026567 | ||||||
chr10:35027143
|
C | CT | 7 | a0001c0001t0001g0044a0001c0001t0001g0117a0001c0001t0003g0030others(4): Show | 7 | HG01169.hp2 HG02615.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1617+1666dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027143 | ||||||
chr10:35027143
|
CT | C | 104 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0269others(101): Show | 109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1617+1666delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027143 | ||||||
chr10:35027143
|
CTT | C | 14 | a0001c0002t0014g0180a0001c0003t0005g0200a0001c0004t0006g0006others(11): Show | 14 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1617+1665_1617+166 others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027143 | ||||||
chr10:35027147
|
T | C | 1 | a0001c0002t0004g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1617+1663A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027147 | ||||||
chr10:35027189
|
G | A | 1 | a0001c0002t0004g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1617+1621C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027189 | ||||||
chr10:35027210
|
A | T | 129 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1617+1600T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027210 | ||||||
chr10:35027324
|
T | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1617+1486A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027324 | ||||||
chr10:35027386
|
C | T | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1617+1424G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027386 | ||||||
chr10:35027387
|
G | A | 1 | a0001c0001t0008g0061 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1617+1423C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027387 | ||||||
chr10:35027560
|
C | G | 1 | a0001c0001t0009g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1617+1250G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027560 | ||||||
chr10:35027653
|
C | T | 1 | a0001c0002t0002g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1617+1157G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027653 | ||||||
chr10:35027875
|
G | C | 3 | a0001c0004t0006g0006a0001c0004t0006g0289a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1617+935C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35027875 | ||||||
chr10:35028337
|
G | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1617+473C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35028337 | ||||||
chr10:35028389
|
C | T | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1617+421G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35028389 | ||||||
chr10:35028484
|
G | A | 1 | a0001c0001t0007g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1617+326C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35028484 | ||||||
chr10:35028621
|
A | G | 1 | a0001c0001t0007g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1617+189T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35028621 | ||||||
chr10:35028634
|
C | T | 284 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1617+176G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 16/20 | chr10 | 35028634 | ||||||
chr10:35028947
|
A | G | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1540-60T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35028947 | ||||||
chr10:35028960
|
T | C | 2 | a0001c0001t0015g0012a0001c0001t0015g0255 | 2 | HG00741.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1540-73A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35028960 | ||||||
chr10:35029063
|
G | GT | 120 | a0001c0001t0001g0026a0001c0001t0001g0261a0001c0001t0011g0235others(117): Show | 125 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1540-177dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35029063 | ||||||
chr10:35029247
|
G | A | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1539+241C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35029247 | ||||||
chr10:35029324
|
T | C | 48 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1539+164A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35029324 | ||||||
chr10:35029393
|
C | T | 1 | a0001c0003t0020g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1539+95G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 15/20 | chr10 | 35029393 | ||||||
chr10:35029659
|
A | G | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-19T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35029659 | ||||||
chr10:35029709
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1387-69A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35029709 | ||||||
chr10:35029714
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1387-74G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35029714 | ||||||
chr10:35029720
|
T | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0073others(4): Show | 7 | HG01255.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-80A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35029720 | ||||||
chr10:35030029
|
C | T | 6 | a0001c0002t0004g0002a0001c0002t0004g0128a0001c0002t0004g0129others(3): Show | 7 | HG01258.hp2 HG01358.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-389G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030029 | ||||||
chr10:35030153
|
T | C | 1 | a0001c0002t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1387-513A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030153 | ||||||
chr10:35030183
|
A | C | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1387-543T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030183 | ||||||
chr10:35030505
|
C | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1386+795G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030505 | ||||||
chr10:35030610
|
T | C | 1 | a0001c0001t0036g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1386+690A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030610 | ||||||
chr10:35030807
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1386+493G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030807 | ||||||
chr10:35030821
|
A | AGGATC | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1386+478_1386+479i others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030821 | ||||||
chr10:35030823
|
T | C | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1386+477A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030823 | ||||||
chr10:35030825
|
A | T | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1386+475T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030825 | ||||||
chr10:35030845
|
T | C | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1386+455A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030845 | ||||||
chr10:35030970
|
C | G | 3 | a0001c0001t0011g0246a0001c0001t0026g0247a0001c0001t0027g0248 | 3 | HG01192.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1386+330G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35030970 | ||||||
chr10:35031252
|
C | T | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+48G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35031252 | ||||||
chr10:35031271
|
G | A | 1 | a0001c0002t0004g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1386+29C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 14/20 | chr10 | 35031271 | ||||||
chr10:35031427
|
T | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-41A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 13/20 | chr10 | 35031427 | ||||||
chr10:35031455
|
C | T | 118 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(115): Show | 123 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1299+36G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 13/20 | chr10 | 35031455 | ||||||
chr10:35031865
|
G | A | 5 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(2): Show | 5 | HG00423.hp2 HG02040.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1171-246C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 12/20 | chr10 | 35031865 | ||||||
chr10:35031987
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1171-368A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 12/20 | chr10 | 35031987 | ||||||
chr10:35032049
|
C | T | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1170+386G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 12/20 | chr10 | 35032049 | ||||||
chr10:35032309
|
T | C | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1170+126A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 12/20 | chr10 | 35032309 | ||||||
chr10:35032824
|
T | C | 5 | a0001c0001t0032g0288a0001c0001t0036g0295a0001c0001t0037g0293others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-330A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 11/20 | chr10 | 35032824 | ||||||
chr10:35032932
|
C | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0102 | 3 | HG02145.hp1 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1110+234G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 11/20 | chr10 | 35032932 | ||||||
chr10:35033096
|
G | A | 122 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(119): Show | 127 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1110+70C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 11/20 | chr10 | 35033096 | ||||||
chr10:35033137
|
T | C | 1 | a0001c0001t0011g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+29A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 11/20 | chr10 | 35033137 | ||||||
chr10:35033149
|
A | G | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+17T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 11/20 | chr10 | 35033149 | ||||||
chr10:35033444
|
T | C | 1 | a0001c0001t0007g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1003-171A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033444 | ||||||
chr10:35033498
|
A | T | 1 | a0001c0001t0007g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1003-225T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033498 | ||||||
chr10:35033511
|
C | T | 1 | a0001c0002t0004g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1003-238G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033511 | ||||||
chr10:35033732
|
G | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1003-459C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033732 | ||||||
chr10:35033755
|
AC | A | 81 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(78): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1003-483delG | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033755 | ||||||
chr10:35033756
|
CA | C | 201 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 201 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1003-484delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033756 | ||||||
chr10:35033760
|
A | C | 3 | a0001c0001t0009g0228a0001c0001t0019g0215a0001c0001t0019g0216 | 3 | HG02559.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1003-487T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033760 | ||||||
chr10:35033788
|
CT | C | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1003-516delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35033788 | ||||||
chr10:35034001
|
A | G | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-728T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034001 | ||||||
chr10:35034028
|
C | T | 1 | a0001c0001t0003g0258 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1003-755G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034028 | ||||||
chr10:35034076
|
C | A | 1 | a0001c0001t0019g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1003-803G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034076 | ||||||
chr10:35034146
|
T | C | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1003-873A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034146 | ||||||
chr10:35034202
|
C | T | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1003-929G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034202 | ||||||
chr10:35034255
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0029 | 3 | NA19057.hp1 NA19076.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1002+917C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034255 | ||||||
chr10:35034288
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1002+884A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034288 | ||||||
chr10:35034340
|
A | G | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1002+832T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034340 | ||||||
chr10:35034459
|
C | T | 2 | a0001c0003t0005g0209a0001c0003t0005g0210 | 2 | NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1002+713G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034459 | ||||||
chr10:35034486
|
G | A | 2 | a0001c0003t0020g0176a0001c0003t0020g0177 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1002+686C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034486 | ||||||
chr10:35034505
|
C | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1002+667G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034505 | ||||||
chr10:35034632
|
T | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002+540A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034632 | ||||||
chr10:35034668
|
C | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | NA18612.hp1 NA18946.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1002+504G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034668 | ||||||
chr10:35034677
|
T | C | 1 | a0001c0001t0008g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1002+495A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034677 | ||||||
chr10:35034693
|
G | A | 1 | a0001c0001t0019g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1002+479C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034693 | ||||||
chr10:35034708
|
G | A | 145 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 145 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1002+464C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034708 | ||||||
chr10:35034815
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0090 | 3 | HG02056.hp1 NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1002+357C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034815 | ||||||
chr10:35034858
|
T | C | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1002+314A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034858 | ||||||
chr10:35034900
|
A | C | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+272T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35034900 | ||||||
chr10:35035124
|
G | A | 3 | a0001c0003t0010g0004a0001c0003t0010g0189a0001c0003t0010g0212 | 4 | HG03491.hp1 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+48C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35035124 | ||||||
chr10:35035148
|
A | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1002+24T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 10/20 | chr10 | 35035148 | ||||||
chr10:35035351
|
TAATATAT others(20): Show |
T | 1 | a0001c0001t0019g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.878-82_878-56delGT others(25): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035351 | ||||||
chr10:35035386
|
G | A | 7 | a0001c0003t0005g0194a0001c0003t0005g0197a0001c0003t0005g0198others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.878-90C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035386 | ||||||
chr10:35035440
|
C | A | 1 | a0001c0004t0006g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.878-144G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035440 | ||||||
chr10:35035657
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.878-361T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035657 | ||||||
chr10:35035691
|
C | T | 110 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(107): Show | 115 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.878-395G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035691 | ||||||
chr10:35035936
|
T | C | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.878-640A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35035936 | ||||||
chr10:35036148
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.878-852G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036148 | ||||||
chr10:35036367
|
T | C | 1 | a0001c0004t0006g0290 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.878-1071A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036367 | ||||||
chr10:35036456
|
G | C | 2 | a0001c0001t0008g0087a0001c0001t0008g0118 | 2 | HG00621.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.878-1160C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036456 | ||||||
chr10:35036465
|
A | AT | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.878-1170dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036465 | ||||||
chr10:35036465
|
A | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.878-1169T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036465 | ||||||
chr10:35036544
|
G | C | 1 | a0001c0003t0020g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.878-1248C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036544 | ||||||
chr10:35036662
|
T | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.878-1366A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35036662 | ||||||
chr10:35037003
|
A | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.878-1707T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037003 | ||||||
chr10:35037145
|
T | A | 7 | a0001c0003t0005g0194a0001c0003t0005g0197a0001c0003t0005g0198others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.877+1775A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037145 | ||||||
chr10:35037305
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877+1615C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037305 | ||||||
chr10:35037335
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.877+1585A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037335 | ||||||
chr10:35037422
|
G | A | 1 | a0001c0001t0015g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.877+1498C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037422 | ||||||
chr10:35037466
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.877+1454G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037466 | ||||||
chr10:35037591
|
A | G | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.877+1329T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037591 | ||||||
chr10:35037627
|
C | T | 9 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(6): Show | 9 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+1293G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037627 | ||||||
chr10:35037682
|
A | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0029others(3): Show | 6 | HG02004.hp1 NA18961.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+1238T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037682 | ||||||
chr10:35037767
|
C | CA | 4 | a0001c0001t0003g0019a0001c0001t0003g0060a0001c0001t0003g0076others(1): Show | 4 | NA18947.hp1 NA18948.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+1152dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037767 | ||||||
chr10:35037795
|
A | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.877+1125T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037795 | ||||||
chr10:35037861
|
G | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.877+1059C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037861 | ||||||
chr10:35037881
|
C | T | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.877+1039G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037881 | ||||||
chr10:35037918
|
C | G | 1 | a0001c0001t0016g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.877+1002G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35037918 | ||||||
chr10:35038005
|
T | G | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+915A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038005 | ||||||
chr10:35038043
|
C | T | 1 | a0001c0002t0004g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.877+877G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038043 | ||||||
chr10:35038056
|
G | A | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.877+864C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038056 | ||||||
chr10:35038065
|
G | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+855C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038065 | ||||||
chr10:35038231
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.877+689A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038231 | ||||||
chr10:35038248
|
G | A | 1 | a0001c0002t0004g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.877+672C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038248 | ||||||
chr10:35038251
|
C | A | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.877+669G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038251 | ||||||
chr10:35038380
|
G | C | 1 | a0001c0002t0004g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.877+540C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038380 | ||||||
chr10:35038470
|
G | A | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.877+450C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038470 | ||||||
chr10:35038525
|
C | CA | 60 | a0001c0001t0003g0019a0001c0001t0003g0022a0001c0001t0003g0027others(57): Show | 64 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.877+394dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038525 | ||||||
chr10:35038525
|
C | CAA | 124 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.877+393_877+394dup others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038525 | ||||||
chr10:35038525
|
C | CAAA | 59 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0044others(56): Show | 59 | HG00423.hp1 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.877+392_877+394dup others(3): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038525 | ||||||
chr10:35038525
|
C | CAAAA | 19 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0091others(16): Show | 20 | HG00741.hp2 HG01884.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.877+391_877+394dup others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038525 | ||||||
chr10:35038525
|
C | CAAAAA | 12 | a0001c0001t0011g0237a0001c0001t0011g0241a0001c0001t0011g0246others(9): Show | 12 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.877+390_877+394dup others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038525 | ||||||
chr10:35038671
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.877+249T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038671 | ||||||
chr10:35038767
|
G | C | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.877+153C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038767 | ||||||
chr10:35038838
|
G | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.877+82C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 9/20 | chr10 | 35038838 | ||||||
chr10:35039160
|
A | G | 133 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(130): Show | 138 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.715-78T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039160 | ||||||
chr10:35039301
|
G | A | 1 | a0001c0004t0006g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.715-219C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039301 | ||||||
chr10:35039357
|
T | C | 1 | a0001c0002t0002g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.715-275A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039357 | ||||||
chr10:35039401
|
G | T | 1 | a0001c0002t0002g0275 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.715-319C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039401 | ||||||
chr10:35039427
|
GT | G | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.715-346delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039427 | ||||||
chr10:35039558
|
T | G | 1 | a0001c0001t0007g0103 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.715-476A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039558 | ||||||
chr10:35039633
|
G | C | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-551C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039633 | ||||||
chr10:35039746
|
T | C | 2 | a0001c0001t0009g0222a0001c0001t0009g0224 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.715-664A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039746 | ||||||
chr10:35039781
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0013 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.715-699C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039781 | ||||||
chr10:35039791
|
G | A | 1 | a0001c0004t0006g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.715-709C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039791 | ||||||
chr10:35039809
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-727G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039809 | ||||||
chr10:35039856
|
AAAAAAT | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-780_715-775del others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039856 | ||||||
chr10:35039874
|
C | T | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.715-792G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039874 | ||||||
chr10:35039919
|
G | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.715-837C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039919 | ||||||
chr10:35039949
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.715-867A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039949 | ||||||
chr10:35039972
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0073others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-890C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35039972 | ||||||
chr10:35040052
|
C | T | 71 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(68): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.715-970G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040052 | ||||||
chr10:35040164
|
T | A | 22 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.715-1082A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040164 | ||||||
chr10:35040182
|
A | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.715-1100T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040182 | ||||||
chr10:35040298
|
C | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-1216G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040298 | ||||||
chr10:35040568
|
T | A | 1 | a0001c0002t0002g0170 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.715-1486A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040568 | ||||||
chr10:35040726
|
G | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-1644C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040726 | ||||||
chr10:35040807
|
A | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.715-1725T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040807 | ||||||
chr10:35040813
|
C | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.715-1731G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040813 | ||||||
chr10:35040829
|
C | T | 1 | a0001c0002t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.715-1747G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040829 | ||||||
chr10:35040859
|
G | A | 1 | a0001c0004t0006g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.715-1777C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040859 | ||||||
chr10:35040902
|
A | G | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.715-1820T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35040902 | ||||||
chr10:35041317
|
A | G | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.715-2235T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041317 | ||||||
chr10:35041418
|
G | A | 1 | a0001c0004t0006g0244 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.715-2336C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041418 | ||||||
chr10:35041464
|
T | C | 1 | a0001c0002t0004g0129 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.715-2382A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041464 | ||||||
chr10:35041473
|
A | G | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2391T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041473 | ||||||
chr10:35041539
|
C | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | NA18612.hp1 NA18946.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-2457G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041539 | ||||||
chr10:35041545
|
CTTTCT | C | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.715-2468_715-2464d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041545 | ||||||
chr10:35041649
|
C | T | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.715-2567G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041649 | ||||||
chr10:35041783
|
C | T | 1 | a0001c0001t0009g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.715-2701G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041783 | ||||||
chr10:35041805
|
G | C | 2 | a0001c0003t0005g0197a0001c0003t0005g0198 | 2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.715-2723C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041805 | ||||||
chr10:35041835
|
C | A | 1 | a0001c0003t0005g0210 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.714+2731G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041835 | ||||||
chr10:35041965
|
A | G | 1 | a0001c0008t0033g0106 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.714+2601T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041965 | ||||||
chr10:35041989
|
A | T | 2 | a0001c0001t0012g0238a0001c0001t0012g0239 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.714+2577T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35041989 | ||||||
chr10:35042095
|
C | G | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.714+2471G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042095 | ||||||
chr10:35042122
|
TCATTACC others(1257): Show |
T | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.714+1180_714+2443d others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042122 | ||||||
chr10:35042131
|
C | T | 2 | a0001c0001t0009g0222a0001c0001t0009g0224 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.714+2435G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042131 | ||||||
chr10:35042307
|
G | T | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.714+2259C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042307 | ||||||
chr10:35042407
|
A | G | 1 | a0001c0003t0020g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.714+2159T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042407 | ||||||
chr10:35042411
|
C | T | 2 | a0001c0001t0018g0046a0002c0007t0018g0053 | 2 | HG02602.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.714+2155G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042411 | ||||||
chr10:35042535
|
T | C | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.714+2031A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042535 | ||||||
chr10:35042696
|
G | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.714+1870C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042696 | ||||||
chr10:35042863
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.714+1703G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042863 | ||||||
chr10:35042875
|
C | T | 1 | a0001c0001t0013g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.714+1691G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042875 | ||||||
chr10:35042993
|
G | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.714+1573C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35042993 | ||||||
chr10:35043006
|
G | A | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.714+1560C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043006 | ||||||
chr10:35043236
|
C | T | 120 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(117): Show | 125 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.714+1330G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043236 | ||||||
chr10:35043412
|
C | A | 1 | a0001c0004t0006g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+1154G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043412 | ||||||
chr10:35043541
|
C | T | 5 | a0001c0001t0032g0288a0001c0001t0036g0295a0001c0001t0037g0293others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+1025G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043541 | ||||||
chr10:35043546
|
C | T | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+1020G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043546 | ||||||
chr10:35043693
|
A | C | 129 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.714+873T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043693 | ||||||
chr10:35043769
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(1): Show | 4 | NA18612.hp1 NA18946.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+797A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043769 | ||||||
chr10:35043864
|
C | G | 1 | a0001c0001t0008g0061 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.714+702G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35043864 | ||||||
chr10:35044049
|
T | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.714+517A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044049 | ||||||
chr10:35044051
|
C | CA | 31 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0059others(28): Show | 31 | HG00423.hp1 HG00741.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.714+514dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044051 | ||||||
chr10:35044051
|
CA | C | 15 | a0001c0001t0003g0030a0001c0001t0003g0063a0001c0001t0007g0280others(12): Show | 15 | HG01169.hp2 HG01358.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.714+514delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044051 | ||||||
chr10:35044051
|
CAA | C | 61 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(58): Show | 65 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.714+513_714+514del others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044051 | ||||||
chr10:35044051
|
CAAAAAAA | C | 28 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(25): Show | 29 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.714+508_714+514del others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044051 | ||||||
chr10:35044051
|
CAAAAAAA others(5): Show |
C | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+503_714+514del others(12): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044051 | ||||||
chr10:35044064
|
A | AAAC | 9 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+501_714+502ins others(3): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044064 | ||||||
chr10:35044145
|
T | A | 1 | a0001c0003t0005g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.714+421A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 8/20 | chr10 | 35044145 | ||||||
chr10:35044695
|
T | A | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.604-19A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 7/20 | chr10 | 35044695 | ||||||
chr10:35044963
|
G | A | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-95C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35044963 | ||||||
chr10:35045183
|
T | C | 1 | a0001c0002t0004g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.507-315A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045183 | ||||||
chr10:35045402
|
T | TAGAGC | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.507-539_507-535dup others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045402 | ||||||
chr10:35045456
|
G | A | 1 | a0001c0002t0004g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.507-588C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045456 | ||||||
chr10:35045545
|
C | CA | 94 | a0001c0001t0001g0024a0001c0001t0001g0098a0001c0001t0003g0009others(91): Show | 98 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.507-678dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045545 | ||||||
chr10:35045545
|
C | CAA | 29 | a0001c0002t0004g0128a0001c0002t0004g0168a0001c0003t0005g0192others(26): Show | 30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.507-679_507-678dup others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045545 | ||||||
chr10:35045606
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.507-738A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045606 | ||||||
chr10:35045667
|
C | T | 118 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(115): Show | 123 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.507-799G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045667 | ||||||
chr10:35045685
|
C | G | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.507-817G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045685 | ||||||
chr10:35045796
|
T | A | 1 | a0001c0001t0031g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.507-928A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045796 | ||||||
chr10:35045821
|
T | C | 1 | a0001c0003t0028g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.507-953A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35045821 | ||||||
chr10:35046057
|
C | T | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.507-1189G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046057 | ||||||
chr10:35046116
|
C | A | 139 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(136): Show | 144 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.507-1248G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046116 | ||||||
chr10:35046181
|
T | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.507-1313A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046181 | ||||||
chr10:35046186
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0013 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.507-1318T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046186 | ||||||
chr10:35046252
|
G | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0024others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.507-1384C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046252 | ||||||
chr10:35046530
|
A | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.507-1662T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046530 | ||||||
chr10:35046744
|
T | C | 22 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.507-1876A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046744 | ||||||
chr10:35046799
|
G | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.507-1931C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046799 | ||||||
chr10:35046848
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.507-1980C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046848 | ||||||
chr10:35046854
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.507-1986G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046854 | ||||||
chr10:35046891
|
T | TCAAAA | 8 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0040others(5): Show | 8 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-2028_507-2024d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046891 | ||||||
chr10:35046891
|
TCAAAA | T | 25 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0068others(22): Show | 25 | HG01071.hp1 HG01099.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.507-2028_507-2024d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046891 | ||||||
chr10:35046891
|
TCAAAACA others(3): Show |
T | 124 | a0001c0001t0003g0048a0001c0001t0011g0235a0001c0001t0011g0236others(121): Show | 129 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.507-2033_507-2024d others(12): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046891 | ||||||
chr10:35046990
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.507-2122A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35046990 | ||||||
chr10:35047181
|
A | G | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.507-2313T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047181 | ||||||
chr10:35047235
|
C | A | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.507-2367G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047235 | ||||||
chr10:35047360
|
C | T | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.506+2323G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047360 | ||||||
chr10:35047426
|
C | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.506+2257G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047426 | ||||||
chr10:35047446
|
T | TA | 16 | a0001c0001t0001g0113a0001c0001t0001g0261a0001c0001t0003g0009others(13): Show | 16 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.506+2236dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047446 | ||||||
chr10:35047588
|
C | A | 1 | a0001c0003t0010g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.506+2095G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047588 | ||||||
chr10:35047607
|
C | CA | 117 | a0001c0001t0001g0070a0001c0001t0001g0100a0001c0001t0001g0117others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.506+2075dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047607 | ||||||
chr10:35047607
|
C | CAA | 6 | a0001c0001t0026g0247a0001c0001t0027g0248a0001c0002t0029g0134others(3): Show | 6 | HG01123.hp2 HG01981.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+2074_506+2075d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047607 | ||||||
chr10:35047700
|
TTGAGG | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.506+1978_506+1982d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047700 | ||||||
chr10:35047818
|
T | C | 3 | a0001c0004t0006g0006a0001c0004t0006g0289a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.506+1865A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047818 | ||||||
chr10:35047888
|
G | C | 1 | a0001c0003t0005g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.506+1795C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35047888 | ||||||
chr10:35048217
|
T | TCTAC | 129 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.506+1465_506+1466i others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048217 | ||||||
chr10:35048288
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.506+1395C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048288 | ||||||
chr10:35048467
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.506+1216T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048467 | ||||||
chr10:35048509
|
A | G | 1 | a0001c0001t0008g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.506+1174T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048509 | ||||||
chr10:35048887
|
T | C | 3 | a0001c0002t0002g0147a0001c0002t0002g0165a0001c0002t0014g0149 | 3 | NA18961.hp2 NA18967.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.506+796A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048887 | ||||||
chr10:35048963
|
G | C | 1 | a0001c0001t0013g0265 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.506+720C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35048963 | ||||||
chr10:35049097
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.506+586A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049097 | ||||||
chr10:35049327
|
C | G | 2 | a0001c0005t0001g0230a0001c0005t0001g0279 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.506+356G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049327 | ||||||
chr10:35049435
|
A | G | 4 | a0001c0001t0036g0295a0001c0001t0037g0293a0001c0001t0038g0292others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+248T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049435 | ||||||
chr10:35049500
|
AAAG | A | 139 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(136): Show | 144 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.506+180_506+182del others(3): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049500 | ||||||
chr10:35049631
|
A | AT | 17 | a0001c0001t0009g0228a0001c0001t0011g0235a0001c0001t0011g0236others(14): Show | 17 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.506+51dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049631 | ||||||
chr10:35049676
|
C | G | 1 | a0001c0002t0004g0172 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.506+7G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 6/20 | chr10 | 35049676 | ||||||
chr10:35049771
|
G | A | 130 | a0001c0001t0009g0225a0001c0001t0011g0235a0001c0001t0011g0236others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
splice_region_variant&intron_variant | LOW | c.424-6C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35049771 | ||||||
chr10:35049922
|
A | AGAAAACA others(1625): Show |
2 | a0001c0005t0001g0230a0001c0005t0001g0279 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424-158_424-157ins others(1632): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35049922 | ||||||
chr10:35049922
|
A | AGAAAACA others(1626): Show |
1 | a0001c0005t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424-158_424-157ins others(1633): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35049922 | ||||||
chr10:35049997
|
T | C | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.424-232A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35049997 | ||||||
chr10:35050025
|
A | T | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424-260T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050025 | ||||||
chr10:35050133
|
T | A | 204 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(201): Show | 209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.424-368A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050133 | ||||||
chr10:35050310
|
G | A | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-545C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050310 | ||||||
chr10:35050322
|
C | CA | 37 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0263others(34): Show | 38 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.424-558dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050322 | ||||||
chr10:35050335
|
A | C | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-570T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050335 | ||||||
chr10:35050396
|
C | A | 121 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(118): Show | 126 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.424-631G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050396 | ||||||
chr10:35050501
|
C | T | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.424-736G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050501 | ||||||
chr10:35050685
|
T | C | 2 | a0001c0002t0002g0175a0001c0002t0017g0126 | 2 | HG02040.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.424-920A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050685 | ||||||
chr10:35050881
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.424-1116G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35050881 | ||||||
chr10:35051028
|
C | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.424-1263G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051028 | ||||||
chr10:35051081
|
T | C | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.424-1316A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051081 | ||||||
chr10:35051171
|
G | A | 1 | a0001c0002t0004g0141 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.424-1406C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051171 | ||||||
chr10:35051175
|
C | T | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.424-1410G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051175 | ||||||
chr10:35051277
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.424-1512A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051277 | ||||||
chr10:35051332
|
G | A | 2 | a0001c0003t0005g0192a0001c0003t0005g0193 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.424-1567C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051332 | ||||||
chr10:35051338
|
G | A | 1 | a0001c0001t0016g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.424-1573C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051338 | ||||||
chr10:35051437
|
T | A | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-1672A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051437 | ||||||
chr10:35051471
|
G | A | 4 | a0001c0001t0008g0028a0001c0001t0008g0047a0001c0001t0008g0094others(1): Show | 4 | HG00544.hp2 HG00609.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-1706C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051471 | ||||||
chr10:35051631
|
A | G | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.424-1866T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051631 | ||||||
chr10:35051652
|
G | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.424-1887C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051652 | ||||||
chr10:35051897
|
G | C | 9 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(6): Show | 9 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-2132C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051897 | ||||||
chr10:35051936
|
G | A | 1 | a0001c0001t0008g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.424-2171C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35051936 | ||||||
chr10:35052373
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.423+2061C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052373 | ||||||
chr10:35052425
|
T | G | 1 | a0001c0001t0039g0294 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.423+2009A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052425 | ||||||
chr10:35052677
|
C | T | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.423+1757G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052677 | ||||||
chr10:35052735
|
T | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.423+1699A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052735 | ||||||
chr10:35052752
|
G | A | 9 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(6): Show | 9 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+1682C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052752 | ||||||
chr10:35052863
|
C | A | 1 | a0001c0001t0008g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.423+1571G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052863 | ||||||
chr10:35052882
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.423+1552C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052882 | ||||||
chr10:35052907
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.423+1527C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052907 | ||||||
chr10:35052907
|
GA | G | 18 | a0001c0001t0001g0024a0001c0001t0007g0280a0001c0001t0007g0282others(15): Show | 18 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.423+1526delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35052907 | ||||||
chr10:35053027
|
G | C | 1 | a0001c0001t0008g0087 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.423+1407C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053027 | ||||||
chr10:35053035
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.423+1399A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053035 | ||||||
chr10:35053069
|
C | T | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+1365G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053069 | ||||||
chr10:35053121
|
A | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.423+1313T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053121 | ||||||
chr10:35053159
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.423+1275C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053159 | ||||||
chr10:35053301
|
C | G | 1 | a0001c0001t0036g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.423+1133G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053301 | ||||||
chr10:35053438
|
CCTA | C | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.423+993_423+995del others(3): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053438 | ||||||
chr10:35053540
|
G | C | 9 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(6): Show | 9 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+894C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053540 | ||||||
chr10:35053912
|
T | C | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+522A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053912 | ||||||
chr10:35053969
|
A | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.423+465T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053969 | ||||||
chr10:35053995
|
G | A | 1 | a0001c0002t0004g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.423+439C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35053995 | ||||||
chr10:35054031
|
C | T | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.423+403G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35054031 | ||||||
chr10:35054063
|
T | TA | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+370dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35054063 | ||||||
chr10:35054156
|
G | A | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.423+278C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35054156 | ||||||
chr10:35054182
|
T | C | 12 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(9): Show | 12 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.423+252A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35054182 | ||||||
chr10:35054269
|
C | CCT | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.423+163_423+164dup others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 5/20 | chr10 | 35054269 | ||||||
chr10:35054569
|
T | C | 13 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.318-30A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35054569 | ||||||
chr10:35054597
|
G | A | 140 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(137): Show | 145 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.318-58C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35054597 | ||||||
chr10:35054728
|
C | T | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.318-189G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35054728 | ||||||
chr10:35054963
|
T | C | 1 | a0001c0001t0023g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.318-424A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35054963 | ||||||
chr10:35055018
|
G | A | 1 | a0001c0001t0019g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.318-479C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055018 | ||||||
chr10:35055374
|
C | T | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-835G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055374 | ||||||
chr10:35055426
|
G | T | 1 | a0001c0001t0013g0265 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.318-887C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055426 | ||||||
chr10:35055470
|
C | T | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.318-931G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055470 | ||||||
chr10:35055471
|
G | A | 1 | a0001c0002t0004g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318-932C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055471 | ||||||
chr10:35055486
|
G | C | 1 | a0001c0001t0038g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.318-947C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055486 | ||||||
chr10:35055565
|
A | G | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.318-1026T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055565 | ||||||
chr10:35055741
|
CT | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.318-1203delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055741 | ||||||
chr10:35055827
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0015g0012a0001c0001t0015g0255 | 3 | HG00741.hp1 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.318-1288A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055827 | ||||||
chr10:35055979
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.318-1440A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055979 | ||||||
chr10:35055980
|
G | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.318-1441C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35055980 | ||||||
chr10:35056041
|
C | T | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.318-1502G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056041 | ||||||
chr10:35056229
|
G | A | 1 | a0001c0001t0013g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.318-1690C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056229 | ||||||
chr10:35056414
|
C | T | 2 | a0001c0001t0018g0046a0002c0007t0018g0053 | 2 | HG02602.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.318-1875G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056414 | ||||||
chr10:35056493
|
G | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG00280.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.318-1954C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056493 | ||||||
chr10:35056507
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.318-1968C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056507 | ||||||
chr10:35056754
|
T | C | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318-2215A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056754 | ||||||
chr10:35056831
|
C | T | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.318-2292G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056831 | ||||||
chr10:35056854
|
A | G | 9 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(6): Show | 9 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-2315T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056854 | ||||||
chr10:35056946
|
C | T | 5 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0163others(2): Show | 5 | HG00423.hp2 HG02040.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.318-2407G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35056946 | ||||||
chr10:35057121
|
A | G | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.318-2582T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057121 | ||||||
chr10:35057198
|
G | T | 7 | a0001c0002t0004g0130a0001c0002t0004g0131a0001c0002t0004g0137others(4): Show | 7 | HG00639.hp1 HG01069.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.318-2659C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057198 | ||||||
chr10:35057700
|
T | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.318-3161A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057700 | ||||||
chr10:35057783
|
C | A | 8 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(5): Show | 8 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+3091G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057783 | ||||||
chr10:35057796
|
T | G | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.317+3078A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057796 | ||||||
chr10:35057810
|
T | TG | 140 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(137): Show | 145 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.317+3063dupC | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057810 | ||||||
chr10:35057819
|
C | A | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.317+3055G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057819 | ||||||
chr10:35057820
|
G | C | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+3054C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057820 | ||||||
chr10:35057966
|
C | T | 4 | a0001c0001t0003g0054a0001c0001t0003g0086a0001c0001t0003g0115others(1): Show | 4 | HG01255.hp2 HG01928.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+2908G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35057966 | ||||||
chr10:35058052
|
T | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.317+2822A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058052 | ||||||
chr10:35058059
|
C | T | 1 | a0001c0001t0007g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.317+2815G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058059 | ||||||
chr10:35058118
|
A | T | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.317+2756T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058118 | ||||||
chr10:35058499
|
T | C | 1 | a0001c0002t0004g0173 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.317+2375A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058499 | ||||||
chr10:35058513
|
T | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.317+2361A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058513 | ||||||
chr10:35058560
|
G | C | 1 | a0001c0001t0013g0265 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.317+2314C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058560 | ||||||
chr10:35058564
|
A | G | 2 | a0001c0001t0003g0272a0001c0001t0034g0259 | 2 | HG00735.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.317+2310T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058564 | ||||||
chr10:35058779
|
C | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | NA19002.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.317+2095G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058779 | ||||||
chr10:35058932
|
G | C | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.317+1942C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058932 | ||||||
chr10:35058945
|
G | C | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.317+1929C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35058945 | ||||||
chr10:35059120
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.317+1754G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059120 | ||||||
chr10:35059187
|
T | C | 1 | a0001c0001t0007g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.317+1687A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059187 | ||||||
chr10:35059259
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.317+1615A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059259 | ||||||
chr10:35059344
|
C | T | 1 | a0001c0001t0007g0254 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.317+1530G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059344 | ||||||
chr10:35059458
|
A | AT | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.317+1415dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059458 | ||||||
chr10:35059480
|
T | C | 1 | a0001c0001t0011g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.317+1394A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059480 | ||||||
chr10:35059951
|
A | G | 1 | a0001c0001t0008g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.317+923T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059951 | ||||||
chr10:35059976
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.317+898A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059976 | ||||||
chr10:35059982
|
A | G | 124 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(121): Show | 129 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.317+892T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35059982 | ||||||
chr10:35060141
|
G | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0073others(4): Show | 7 | HG01255.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+733C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060141 | ||||||
chr10:35060274
|
A | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.317+600T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060274 | ||||||
chr10:35060376
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.317+498A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060376 | ||||||
chr10:35060578
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0068 | 2 | HG01167.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.317+296A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060578 | ||||||
chr10:35060642
|
C | T | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.317+232G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060642 | ||||||
chr10:35060646
|
C | T | 119 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(116): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.317+228G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 4/20 | chr10 | 35060646 | ||||||
chr10:35061140
|
A | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-172T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061140 | ||||||
chr10:35061211
|
C | T | 1 | a0001c0003t0005g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.223-243G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061211 | ||||||
chr10:35061245
|
G | A | 1 | a0001c0001t0003g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.223-277C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061245 | ||||||
chr10:35061416
|
C | G | 3 | a0001c0001t0016g0055a0001c0001t0016g0081a0001c0001t0016g0116 | 3 | HG00642.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.223-448G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061416 | ||||||
chr10:35061461
|
C | CA | 11 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0261others(8): Show | 11 | HG00735.hp2 HG01071.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-494dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061461 | ||||||
chr10:35061461
|
CA | C | 88 | a0001c0001t0019g0215a0001c0001t0019g0216a0001c0001t0026g0247others(85): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.223-494delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061461 | ||||||
chr10:35061461
|
CAA | C | 7 | a0001c0003t0005g0194a0001c0003t0005g0197a0001c0003t0005g0198others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-495_223-494del others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061461 | ||||||
chr10:35061483
|
A | C | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.223-515T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061483 | ||||||
chr10:35061488
|
T | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.223-520A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061488 | ||||||
chr10:35061559
|
C | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-591G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061559 | ||||||
chr10:35061573
|
C | T | 2 | a0001c0001t0003g0079a0001c0001t0007g0080 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.223-605G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061573 | ||||||
chr10:35061627
|
T | A | 1 | a0001c0001t0009g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.223-659A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061627 | ||||||
chr10:35061769
|
G | GT | 73 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0093others(70): Show | 77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.223-802dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061769 | ||||||
chr10:35061769
|
G | GTT | 13 | a0001c0002t0002g0147a0001c0002t0002g0151a0001c0002t0002g0152others(10): Show | 13 | HG01175.hp1 HG01358.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.223-803_223-802dup others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061769 | ||||||
chr10:35061769
|
G | T | 1 | a0001c0002t0002g0145 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.223-801C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061769 | ||||||
chr10:35061769
|
GT | G | 9 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-802delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061769 | ||||||
chr10:35061871
|
G | A | 1 | a0001c0001t0007g0103 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.223-903C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061871 | ||||||
chr10:35061906
|
C | G | 1 | a0001c0001t0011g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223-938G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061906 | ||||||
chr10:35061934
|
A | G | 1 | a0001c0001t0023g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.223-966T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35061934 | ||||||
chr10:35062088
|
C | T | 4 | a0001c0001t0003g0052a0001c0001t0003g0084a0001c0001t0003g0085others(1): Show | 4 | HG00609.hp1 HG00738.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+872G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062088 | ||||||
chr10:35062089
|
G | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.222+871C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062089 | ||||||
chr10:35062109
|
T | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+851A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062109 | ||||||
chr10:35062227
|
A | G | 140 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(137): Show | 145 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.222+733T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062227 | ||||||
chr10:35062321
|
C | T | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.222+639G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062321 | ||||||
chr10:35062386
|
A | G | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.222+574T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062386 | ||||||
chr10:35062489
|
C | A | 1 | a0001c0004t0006g0290 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.222+471G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062489 | ||||||
chr10:35062568
|
G | A | 2 | a0001c0001t0012g0238a0001c0001t0012g0239 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.222+392C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062568 | ||||||
chr10:35062603
|
C | G | 123 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(120): Show | 128 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.222+357G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062603 | ||||||
chr10:35062670
|
C | CA | 75 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0090others(72): Show | 80 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.222+289dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062670 | ||||||
chr10:35062670
|
CA | C | 10 | a0001c0001t0001g0056a0001c0001t0003g0009a0001c0001t0007g0218others(7): Show | 10 | HG00280.hp2 HG01069.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.222+289delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062670 | ||||||
chr10:35062754
|
G | A | 1 | a0001c0003t0015g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.222+206C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062754 | ||||||
chr10:35062793
|
C | T | 1 | a0001c0001t0003g0062 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.222+167G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 3/20 | chr10 | 35062793 | ||||||
chr10:35063381
|
G | C | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.120-319C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35063381 | ||||||
chr10:35063749
|
C | CT | 17 | a0001c0001t0001g0036a0001c0001t0001g0066a0001c0001t0001g0110others(14): Show | 18 | HG00621.hp2 HG01884.hp1 HG02683.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-688dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35063749 | ||||||
chr10:35063749
|
CT | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0101others(17): Show | 20 | HG00323.hp1 HG01071.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-688delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35063749 | ||||||
chr10:35063806
|
A | G | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120-744T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35063806 | ||||||
chr10:35064029
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.120-967A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064029 | ||||||
chr10:35064049
|
G | T | 1 | a0001c0003t0010g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120-987C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064049 | ||||||
chr10:35064163
|
T | C | 1 | a0001c0002t0004g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.120-1101A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064163 | ||||||
chr10:35064376
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG00280.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.120-1314G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064376 | ||||||
chr10:35064611
|
A | G | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120-1549T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064611 | ||||||
chr10:35064646
|
C | T | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.120-1584G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064646 | ||||||
chr10:35064773
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.120-1711C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35064773 | ||||||
chr10:35065027
|
C | T | 1 | a0001c0001t0011g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.120-1965G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065027 | ||||||
chr10:35065110
|
T | G | 5 | a0001c0001t0009g0221a0001c0001t0009g0223a0001c0001t0009g0276others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.120-2048A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065110 | ||||||
chr10:35065229
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.120-2167C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065229 | ||||||
chr10:35065449
|
T | C | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.120-2387A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065449 | ||||||
chr10:35065543
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.120-2481G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065543 | ||||||
chr10:35065573
|
C | T | 1 | a0001c0002t0004g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.120-2511G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065573 | ||||||
chr10:35065640
|
A | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-2578T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065640 | ||||||
chr10:35065731
|
T | C | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.120-2669A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065731 | ||||||
chr10:35065760
|
G | A | 1 | a0001c0001t0008g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.120-2698C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065760 | ||||||
chr10:35065847
|
G | C | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.120-2785C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065847 | ||||||
chr10:35065853
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.120-2791T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065853 | ||||||
chr10:35065863
|
A | C | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.120-2801T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065863 | ||||||
chr10:35065898
|
A | T | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120-2836T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35065898 | ||||||
chr10:35066103
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.120-3041A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066103 | ||||||
chr10:35066433
|
G | C | 7 | a0001c0001t0011g0236a0001c0001t0012g0231a0001c0001t0012g0232others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.120-3371C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066433 | ||||||
chr10:35066474
|
AT | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.120-3413delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066474 | ||||||
chr10:35066499
|
C | T | 1 | a0001c0004t0006g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120-3437G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066499 | ||||||
chr10:35066632
|
A | G | 1 | a0001c0002t0004g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120-3570T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066632 | ||||||
chr10:35066670
|
G | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.120-3608C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066670 | ||||||
chr10:35066727
|
A | T | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.120-3665T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066727 | ||||||
chr10:35066869
|
T | C | 1 | a0001c0003t0005g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.120-3807A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066869 | ||||||
chr10:35066981
|
T | C | 1 | a0001c0003t0020g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.120-3919A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066981 | ||||||
chr10:35066982
|
G | A | 1 | a0001c0003t0020g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.120-3920C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35066982 | ||||||
chr10:35067139
|
C | CA | 93 | a0001c0001t0001g0044a0001c0001t0008g0047a0001c0002t0002g0001others(90): Show | 98 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.119+4059dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067139 | ||||||
chr10:35067139
|
CA | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0096a0001c0004t0006g0242others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+4059delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067139 | ||||||
chr10:35067153
|
A | AG | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.119+4045_119+4046i others(3): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067153 | ||||||
chr10:35067153
|
A | G | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.119+4046T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067153 | ||||||
chr10:35067228
|
A | G | 1 | a0001c0002t0004g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.119+3971T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067228 | ||||||
chr10:35067673
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.119+3526C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067673 | ||||||
chr10:35067743
|
C | CA | 12 | a0001c0001t0001g0261a0001c0001t0007g0280a0001c0001t0019g0215others(9): Show | 12 | HG01884.hp1 HG02132.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+3455dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067743 | ||||||
chr10:35067743
|
C | CAA | 14 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(11): Show | 14 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.119+3454_119+3455d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067743 | ||||||
chr10:35067846
|
A | G | 117 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.119+3353T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067846 | ||||||
chr10:35067889
|
C | G | 4 | a0001c0001t0008g0061a0001c0001t0008g0078a0001c0001t0008g0108others(1): Show | 4 | HG02074.hp2 HG02280.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+3310G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067889 | ||||||
chr10:35067958
|
A | C | 1 | a0001c0003t0005g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.119+3241T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35067958 | ||||||
chr10:35068003
|
G | A | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.119+3196C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068003 | ||||||
chr10:35068034
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02056.hp1 HG02683.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+3165G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068034 | ||||||
chr10:35068109
|
C | CA | 23 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0043others(20): Show | 23 | HG00423.hp1 HG01891.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+3089dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068109 | ||||||
chr10:35068109
|
CA | C | 117 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(114): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.119+3089delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068109 | ||||||
chr10:35068222
|
G | C | 70 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(67): Show | 74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.119+2977C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068222 | ||||||
chr10:35068272
|
A | G | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.119+2927T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068272 | ||||||
chr10:35068418
|
T | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.119+2781A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068418 | ||||||
chr10:35068973
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.119+2226T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35068973 | ||||||
chr10:35069207
|
G | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.119+1992C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069207 | ||||||
chr10:35069208
|
G | A | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.119+1991C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069208 | ||||||
chr10:35069445
|
A | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+1754T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069445 | ||||||
chr10:35069584
|
A | G | 16 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(13): Show | 16 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.119+1615T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069584 | ||||||
chr10:35069632
|
G | A | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.119+1567C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069632 | ||||||
chr10:35069831
|
C | T | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.119+1368G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35069831 | ||||||
chr10:35070061
|
A | G | 12 | a0001c0004t0006g0006a0001c0004t0006g0242a0001c0004t0006g0243others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.119+1138T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070061 | ||||||
chr10:35070546
|
C | T | 1 | a0001c0002t0002g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.119+653G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070546 | ||||||
chr10:35070547
|
A | G | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.119+652T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070547 | ||||||
chr10:35070573
|
T | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+626A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070573 | ||||||
chr10:35070619
|
A | G | 1 | a0001c0001t0025g0077 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.119+580T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070619 | ||||||
chr10:35070646
|
A | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.119+553T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070646 | ||||||
chr10:35070691
|
A | G | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.119+508T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070691 | ||||||
chr10:35070807
|
C | T | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.119+392G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070807 | ||||||
chr10:35070830
|
C | T | 1 | a0001c0004t0006g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.119+369G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070830 | ||||||
chr10:35070940
|
AT | A | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+258delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 2/20 | chr10 | 35070940 | ||||||
chr10:35071382
|
G | A | 129 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-22-43C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071382 | ||||||
chr10:35071394
|
T | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0029others(3): Show | 6 | HG02004.hp2 NA18961.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-55A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071394 | ||||||
chr10:35071506
|
G | A | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-22-167C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071506 | ||||||
chr10:35071554
|
G | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-22-215C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071554 | ||||||
chr10:35071629
|
T | C | 67 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(64): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-290A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071629 | ||||||
chr10:35071644
|
G | A | 29 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(26): Show | 30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-22-305C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071644 | ||||||
chr10:35071688
|
A | G | 40 | a0001c0001t0001g0071a0001c0001t0009g0221a0001c0001t0009g0276others(37): Show | 40 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-22-349T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071688 | ||||||
chr10:35071692
|
A | G | 144 | a0001c0001t0001g0071a0001c0001t0007g0218a0001c0001t0007g0219others(141): Show | 149 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-22-353T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071692 | ||||||
chr10:35071696
|
T | C | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-22-357A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071696 | ||||||
chr10:35071849
|
C | G | 1 | a0001c0001t0023g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-22-510G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071849 | ||||||
chr10:35071896
|
G | A | 1 | a0001c0001t0013g0265 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22-557C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35071896 | ||||||
chr10:35072372
|
C | CT | 6 | a0001c0001t0013g0274a0001c0002t0002g0147a0001c0002t0014g0169others(3): Show | 6 | HG01071.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-1034dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072372 | ||||||
chr10:35072372
|
CTTTT | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22-1037_-22-1034d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072372 | ||||||
chr10:35072403
|
C | G | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-22-1064G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072403 | ||||||
chr10:35072586
|
C | T | 1 | a0001c0001t0016g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-22-1247G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072586 | ||||||
chr10:35072597
|
T | C | 1 | a0001c0002t0002g0157 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-22-1258A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072597 | ||||||
chr10:35072602
|
T | G | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-22-1263A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072602 | ||||||
chr10:35072830
|
C | T | 1 | a0001c0001t0034g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-22-1491G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072830 | ||||||
chr10:35072929
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0248 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-22-1590A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35072929 | ||||||
chr10:35073008
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-1669C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073008 | ||||||
chr10:35073044
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-22-1705G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073044 | ||||||
chr10:35073277
|
T | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-22-1938A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073277 | ||||||
chr10:35073358
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-2019A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073358 | ||||||
chr10:35073428
|
A | C | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-22-2089T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073428 | ||||||
chr10:35073491
|
C | T | 1 | a0001c0004t0006g0284 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-22-2152G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073491 | ||||||
chr10:35073514
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-22-2175C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073514 | ||||||
chr10:35073524
|
G | A | 3 | a0001c0001t0011g0246a0001c0001t0026g0247a0001c0001t0027g0248 | 3 | HG01192.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-22-2185C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073524 | ||||||
chr10:35073580
|
CTTTTCTT others(5): Show |
C | 1 | a0001c0001t0015g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-22-2253_-22-2242d others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073580 | ||||||
chr10:35073580
|
CTTTTCTT others(17): Show |
C | 1 | a0001c0002t0004g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22-2265_-22-2242d others(26): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073580 | ||||||
chr10:35073590
|
T | C | 45 | a0001c0001t0001g0007a0001c0001t0003g0009a0001c0001t0003g0015others(42): Show | 45 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22-2251A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073590 | ||||||
chr10:35073674
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22-2335C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073674 | ||||||
chr10:35073697
|
T | C | 140 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(137): Show | 145 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-22-2358A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073697 | ||||||
chr10:35073749
|
C | T | 1 | a0001c0001t0003g0062 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-22-2410G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073749 | ||||||
chr10:35073753
|
T | C | 119 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(116): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-22-2414A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073753 | ||||||
chr10:35073766
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-2427C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073766 | ||||||
chr10:35073861
|
C | T | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22-2522G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35073861 | ||||||
chr10:35074049
|
A | G | 130 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-22-2710T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074049 | ||||||
chr10:35074563
|
T | C | 8 | a0001c0001t0003g0052a0001c0001t0003g0054a0001c0001t0003g0084others(5): Show | 8 | HG00609.hp1 HG00738.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-3224A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074563 | ||||||
chr10:35074646
|
A | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-22-3307T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074646 | ||||||
chr10:35074724
|
T | A | 4 | a0001c0001t0008g0028a0001c0001t0008g0047a0001c0001t0008g0094others(1): Show | 4 | HG00544.hp2 HG00609.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-3385A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074724 | ||||||
chr10:35074729
|
C | T | 1 | a0001c0001t0007g0227 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-22-3390G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074729 | ||||||
chr10:35074736
|
C | T | 1 | a0001c0004t0006g0290 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-22-3397G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074736 | ||||||
chr10:35074737
|
T | C | 1 | a0001c0001t0011g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-22-3398A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074737 | ||||||
chr10:35074947
|
T | A | 1 | a0001c0002t0014g0158 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-22-3608A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074947 | ||||||
chr10:35074947
|
T | C | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-22-3608A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35074947 | ||||||
chr10:35075045
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-3706A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075045 | ||||||
chr10:35075176
|
C | T | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-22-3837G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075176 | ||||||
chr10:35075321
|
T | C | 1 | a0001c0001t0016g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-22-3982A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075321 | ||||||
chr10:35075349
|
C | T | 7 | a0001c0003t0005g0194a0001c0003t0005g0197a0001c0003t0005g0198others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-4010G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075349 | ||||||
chr10:35075391
|
A | G | 2 | a0001c0003t0005g0192a0001c0003t0005g0193 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-22-4052T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075391 | ||||||
chr10:35075408
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-22-4069G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075408 | ||||||
chr10:35075411
|
C | G | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-4072G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075411 | ||||||
chr10:35075446
|
T | C | 4 | a0001c0001t0008g0047a0001c0003t0005g0205a0001c0003t0005g0209others(1): Show | 4 | NA18959.hp2 NA18975.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-4107A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075446 | ||||||
chr10:35075462
|
G | A | 2 | a0001c0001t0012g0231a0001c0001t0012g0234 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-22-4123C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075462 | ||||||
chr10:35075511
|
C | T | 8 | a0001c0003t0010g0004a0001c0003t0010g0186a0001c0003t0010g0187others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-4172G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075511 | ||||||
chr10:35075632
|
TA | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0109others(2): Show | 5 | HG01099.hp2 HG02145.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-4294delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075632 | ||||||
chr10:35075634
|
AAAC | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0089a0001c0001t0007g0283others(1): Show | 4 | HG02559.hp1 HG02965.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4298_-22-4296d others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075634 | ||||||
chr10:35075634
|
AAACACAC | A | 4 | a0001c0001t0003g0114a0001c0001t0008g0112a0001c0001t0039g0294others(1): Show | 4 | HG02015.hp1 HG02074.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4302_-22-4296d others(9): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075634 | ||||||
chr10:35075635
|
A | AAC | 26 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0117others(23): Show | 27 | HG00423.hp2 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-22-4298_-22-4297d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
A | AACAC | 15 | a0001c0001t0001g0261a0001c0001t0013g0264a0001c0002t0002g0003others(12): Show | 16 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-4300_-22-4297d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
A | AACACAC | 3 | a0001c0002t0002g0171a0001c0002t0004g0125a0001c0003t0020g0177 | 3 | HG01099.hp1 HG03041.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-22-4302_-22-4297d others(8): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AAC | A | 52 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(49): Show | 54 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-22-4298_-22-4297d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACAC | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0011others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.-22-4300_-22-4297d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACAC | A | 26 | a0001c0001t0001g0100a0001c0001t0001g0113a0001c0001t0003g0015others(23): Show | 26 | HG00609.hp1 HG00642.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-4302_-22-4297d others(8): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACACA others(1): Show |
A | 39 | a0001c0001t0001g0007a0001c0001t0003g0009a0001c0001t0003g0019others(36): Show | 39 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-22-4304_-22-4297d others(10): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACACA others(3): Show |
A | 22 | a0001c0001t0036g0295a0001c0001t0037g0293a0001c0003t0005g0192others(19): Show | 23 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22-4306_-22-4297d others(12): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACACA others(5): Show |
A | 8 | a0001c0001t0008g0087a0001c0002t0002g0183a0001c0003t0005g0208others(5): Show | 8 | HG00621.hp2 HG01109.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22-4308_-22-4297d others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0038g0292a0001c0002t0004g0144 | 2 | HG01258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-22-4310_-22-4297d others(16): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075635
|
AACACACA others(9): Show |
A | 4 | a0001c0001t0001g0088a0001c0004t0006g0006a0001c0004t0006g0289others(1): Show | 4 | HG01071.hp1 HG02572.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-4312_-22-4297d others(18): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075635 | ||||||
chr10:35075680
|
A | G | 1 | a0001c0002t0002g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-22-4341T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075680 | ||||||
chr10:35075855
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-22-4516T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075855 | ||||||
chr10:35075887
|
G | C | 26 | a0001c0002t0002g0001a0001c0002t0002g0124a0001c0002t0002g0145others(23): Show | 28 | HG00544.hp1 HG02015.hp2 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22-4548C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35075887 | ||||||
chr10:35076064
|
G | T | 114 | a0001c0001t0032g0288a0001c0002t0002g0001a0001c0002t0002g0003others(111): Show | 119 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-22-4725C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076064 | ||||||
chr10:35076192
|
G | T | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-22-4853C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076192 | ||||||
chr10:35076323
|
T | C | 1 | a0001c0001t0009g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-22-4984A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076323 | ||||||
chr10:35076419
|
A | C | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-22-5080T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076419 | ||||||
chr10:35076545
|
A | G | 1 | a0001c0001t0013g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-22-5206T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076545 | ||||||
chr10:35076571
|
G | A | 13 | a0001c0002t0002g0003a0001c0002t0002g0121a0001c0002t0002g0122others(10): Show | 14 | HG00423.hp2 HG02040.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22-5232C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076571 | ||||||
chr10:35076576
|
C | T | 1 | a0001c0001t0008g0061 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-22-5237G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076576 | ||||||
chr10:35076777
|
C | T | 106 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(103): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-22-5438G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076777 | ||||||
chr10:35076847
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-22-5508G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076847 | ||||||
chr10:35076866
|
T | C | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-22-5527A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076866 | ||||||
chr10:35076943
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG00280.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-22-5604A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35076943 | ||||||
chr10:35077137
|
T | G | 1 | a0001c0001t0008g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-22-5798A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077137 | ||||||
chr10:35077305
|
C | A | 1 | a0001c0002t0002g0165 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-22-5966G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077305 | ||||||
chr10:35077314
|
A | G | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-5975T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077314 | ||||||
chr10:35077326
|
C | CA | 28 | a0001c0002t0002g0166a0001c0003t0005g0194a0001c0003t0005g0195others(25): Show | 29 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-5988dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077326 | ||||||
chr10:35077330
|
C | A | 109 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(106): Show | 114 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-22-5991G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077330 | ||||||
chr10:35077355
|
G | A | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-22-6016C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077355 | ||||||
chr10:35077411
|
C | T | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-22-6072G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077411 | ||||||
chr10:35077419
|
C | G | 2 | a0001c0003t0005g0197a0001c0003t0005g0198 | 2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-22-6080G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077419 | ||||||
chr10:35077419
|
C | T | 4 | a0001c0001t0012g0231a0001c0001t0012g0232a0001c0001t0012g0233others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-6080G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077419 | ||||||
chr10:35077434
|
T | C | 2 | a0001c0001t0003g0020a0001c0006t0003g0021 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-22-6095A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077434 | ||||||
chr10:35077534
|
G | C | 119 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(116): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-22-6195C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077534 | ||||||
chr10:35077584
|
G | A | 1 | a0001c0001t0019g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-22-6245C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077584 | ||||||
chr10:35077748
|
C | T | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-6409G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077748 | ||||||
chr10:35077817
|
C | CA | 70 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(67): Show | 74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-22-6479dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077817 | ||||||
chr10:35077950
|
A | C | 123 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(120): Show | 128 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-22-6611T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35077950 | ||||||
chr10:35078007
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-22-6668A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078007 | ||||||
chr10:35078106
|
C | A | 2 | a0001c0001t0003g0272a0001c0001t0034g0259 | 2 | HG00735.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22-6767G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078106 | ||||||
chr10:35078233
|
T | C | 119 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(116): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-22-6894A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078233 | ||||||
chr10:35078295
|
AT | A | 9 | a0001c0001t0001g0058a0001c0001t0011g0246a0001c0001t0012g0231others(6): Show | 9 | HG01081.hp1 HG01192.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-6957delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078295 | ||||||
chr10:35078390
|
G | C | 1 | a0001c0001t0007g0283 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22-7051C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078390 | ||||||
chr10:35078408
|
G | A | 1 | a0001c0002t0002g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-22-7069C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078408 | ||||||
chr10:35078459
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-22-7120C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078459 | ||||||
chr10:35078490
|
G | A | 1 | a0001c0004t0006g0289 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22-7151C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078490 | ||||||
chr10:35078614
|
A | T | 1 | a0001c0001t0039g0294 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-22-7275T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078614 | ||||||
chr10:35078647
|
G | A | 8 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(5): Show | 8 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22-7308C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078647 | ||||||
chr10:35078787
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-22-7448T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078787 | ||||||
chr10:35078839
|
T | C | 11 | a0001c0001t0011g0235a0001c0001t0011g0236a0001c0001t0011g0237others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-7500A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078839 | ||||||
chr10:35078848
|
C | A | 1 | a0001c0001t0019g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-22-7509G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35078848 | ||||||
chr10:35079105
|
C | T | 1 | a0001c0001t0003g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-22-7766G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079105 | ||||||
chr10:35079175
|
T | C | 1 | a0001c0002t0002g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-22-7836A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079175 | ||||||
chr10:35079214
|
C | T | 3 | a0001c0001t0013g0264a0001c0001t0013g0265a0001c0001t0013g0266 | 3 | HG02735.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-22-7875G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079214 | ||||||
chr10:35079336
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-22-7997A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079336 | ||||||
chr10:35079457
|
A | T | 140 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-22-8118T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079457 | ||||||
chr10:35079471
|
A | G | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-8132T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35079471 | ||||||
chr10:35080016
|
C | T | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-22-8677G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080016 | ||||||
chr10:35080055
|
A | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-8716T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080055 | ||||||
chr10:35080128
|
A | G | 129 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(126): Show | 134 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-22-8789T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080128 | ||||||
chr10:35080222
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-22-8883A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080222 | ||||||
chr10:35080371
|
A | G | 123 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(120): Show | 128 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-22-9032T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080371 | ||||||
chr10:35080402
|
C | T | 1 | a0001c0002t0002g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-22-9063G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080402 | ||||||
chr10:35080433
|
T | TTTTA | 78 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0064others(75): Show | 78 | HG00544.hp2 HG00621.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22-9098_-22-9095d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080433
|
T | TTTTATTT others(1): Show |
11 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(8): Show | 11 | HG00609.hp2 HG00642.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22-9102_-22-9095d others(10): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080433
|
T | TTTTATTT others(5): Show |
1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-22-9106_-22-9095d others(14): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080433
|
TTTTA | T | 90 | a0001c0001t0001g0031a0001c0001t0001g0249a0001c0001t0011g0246others(87): Show | 94 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-22-9098_-22-9095d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080433
|
TTTTATTT others(1): Show |
T | 16 | a0001c0001t0009g0221a0001c0001t0009g0222a0001c0001t0009g0223others(13): Show | 16 | HG00639.hp2 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-9102_-22-9095d others(10): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080433
|
TTTTATTT others(9): Show |
T | 10 | a0001c0001t0001g0011a0001c0004t0006g0242a0001c0004t0006g0243others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22-9110_-22-9095d others(18): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080433 | ||||||
chr10:35080625
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG01934.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-22-9286A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080625 | ||||||
chr10:35080745
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-22-9406C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080745 | ||||||
chr10:35080830
|
A | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+9349T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080830 | ||||||
chr10:35080860
|
G | A | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+9319C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080860 | ||||||
chr10:35080968
|
C | T | 3 | a0001c0005t0001g0229a0001c0005t0001g0230a0001c0005t0001g0279 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-23+9211G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35080968 | ||||||
chr10:35081097
|
G | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0094a0001c0001t0008g0260 | 3 | HG00544.hp2 HG00609.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-23+9082C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081097 | ||||||
chr10:35081143
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-23+9036C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081143 | ||||||
chr10:35081185
|
C | T | 1 | a0001c0001t0037g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-23+8994G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081185 | ||||||
chr10:35081447
|
A | T | 31 | a0001c0001t0007g0219a0001c0003t0005g0192a0001c0003t0005g0193others(28): Show | 32 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-23+8732T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081447 | ||||||
chr10:35081515
|
T | C | 123 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(120): Show | 128 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-23+8664A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081515 | ||||||
chr10:35081537
|
G | T | 123 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(120): Show | 128 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-23+8642C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081537 | ||||||
chr10:35081704
|
G | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+8475C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081704 | ||||||
chr10:35081714
|
T | G | 1 | a0001c0001t0003g0015 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-23+8465A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081714 | ||||||
chr10:35081959
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-23+8220T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35081959 | ||||||
chr10:35082015
|
G | A | 1 | a0001c0002t0004g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-23+8164C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082015 | ||||||
chr10:35082195
|
C | A | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-23+7984G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082195 | ||||||
chr10:35082328
|
C | T | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-23+7851G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082328 | ||||||
chr10:35082432
|
A | G | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-23+7747T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082432 | ||||||
chr10:35082448
|
C | T | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+7731G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082448 | ||||||
chr10:35082460
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | NA18612.hp1 NA18946.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+7719C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082460 | ||||||
chr10:35082468
|
T | C | 70 | a0001c0001t0032g0288a0001c0002t0002g0001a0001c0002t0002g0003others(67): Show | 74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-23+7711A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082468 | ||||||
chr10:35082480
|
T | C | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+7699A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082480 | ||||||
chr10:35082543
|
A | G | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+7636T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082543 | ||||||
chr10:35082596
|
G | A | 1 | a0001c0001t0008g0118 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-23+7583C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082596 | ||||||
chr10:35082739
|
CTT | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0273 | 3 | HG00642.hp1 HG01109.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-23+7438_-23+7439d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35082739 | ||||||
chr10:35083039
|
C | A | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-23+7140G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083039 | ||||||
chr10:35083065
|
G | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+7114C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083065 | ||||||
chr10:35083112
|
G | A | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+7067C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083112 | ||||||
chr10:35083154
|
C | CA | 8 | a0001c0001t0001g0263a0001c0001t0011g0235a0001c0001t0011g0236others(5): Show | 8 | HG00621.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+7024dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083154 | ||||||
chr10:35083154
|
CA | C | 8 | a0001c0001t0003g0030a0001c0001t0009g0276a0001c0001t0011g0246others(5): Show | 8 | HG01169.hp2 HG01192.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+7024delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083154 | ||||||
chr10:35083154
|
CAA | C | 99 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(96): Show | 104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-23+7023_-23+7024d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083154 | ||||||
chr10:35083210
|
CCGTCAGA others(16): Show |
C | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+6946_-23+6968d others(25): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083210 | ||||||
chr10:35083212
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-23+6967C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083212 | ||||||
chr10:35083333
|
G | C | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23+6846C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083333 | ||||||
chr10:35083561
|
G | A | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23+6618C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083561 | ||||||
chr10:35083687
|
A | G | 1 | a0001c0003t0020g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-23+6492T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083687 | ||||||
chr10:35083806
|
C | T | 22 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+6373G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35083806 | ||||||
chr10:35084052
|
G | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+6127C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084052 | ||||||
chr10:35084231
|
C | T | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+5948G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084231 | ||||||
chr10:35084833
|
T | G | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+5346A>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084833 | ||||||
chr10:35084844
|
G | C | 3 | a0001c0001t0013g0264a0001c0001t0013g0265a0001c0001t0013g0266 | 3 | HG02735.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-23+5335C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084844 | ||||||
chr10:35084845
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-23+5334G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084845 | ||||||
chr10:35084886
|
G | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+5293C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084886 | ||||||
chr10:35084951
|
C | T | 1 | a0001c0003t0010g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-23+5228G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35084951 | ||||||
chr10:35085051
|
C | T | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+5128G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085051 | ||||||
chr10:35085155
|
G | A | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+5024C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085155 | ||||||
chr10:35085255
|
C | T | 1 | a0001c0002t0004g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-23+4924G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085255 | ||||||
chr10:35085256
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-23+4923C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085256 | ||||||
chr10:35085381
|
G | C | 1 | a0001c0004t0006g0290 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-23+4798C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085381 | ||||||
chr10:35085422
|
A | T | 114 | a0001c0001t0032g0288a0001c0002t0002g0001a0001c0002t0002g0003others(111): Show | 119 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-23+4757T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085422 | ||||||
chr10:35085430
|
A | C | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+4749T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085430 | ||||||
chr10:35085431
|
A | G | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+4748T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085431 | ||||||
chr10:35085434
|
AAAAAT | A | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+4740_-23+4744d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085434 | ||||||
chr10:35085520
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-23+4659C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085520 | ||||||
chr10:35085547
|
A | C | 1 | a0001c0001t0011g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-23+4632T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085547 | ||||||
chr10:35085617
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23+4562C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085617 | ||||||
chr10:35085637
|
G | A | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+4542C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085637 | ||||||
chr10:35085649
|
C | A | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+4530G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085649 | ||||||
chr10:35085666
|
G | A | 1 | a0001c0001t0011g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-23+4513C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085666 | ||||||
chr10:35085695
|
T | C | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+4484A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085695 | ||||||
chr10:35085696
|
C | CA | 19 | a0001c0001t0001g0013a0001c0001t0001g0269a0001c0001t0001g0270others(16): Show | 19 | HG01884.hp1 HG02132.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+4482dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085696 | ||||||
chr10:35085696
|
C | T | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+4483G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085696 | ||||||
chr10:35085696
|
CA | C | 12 | a0001c0001t0001g0029a0001c0001t0003g0015a0001c0001t0032g0288others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+4482delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085696 | ||||||
chr10:35085697
|
A | C | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+4482T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085697 | ||||||
chr10:35085724
|
A | T | 1 | a0001c0001t0008g0028 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-23+4455T>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085724 | ||||||
chr10:35085892
|
G | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+4287C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085892 | ||||||
chr10:35085975
|
C | G | 1 | a0001c0001t0032g0288 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-23+4204G>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085975 | ||||||
chr10:35085980
|
G | A | 1 | a0001c0001t0023g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-23+4199C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35085980 | ||||||
chr10:35086124
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-23+4055C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086124 | ||||||
chr10:35086164
|
A | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+4015T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086164 | ||||||
chr10:35086177
|
A | C | 1 | a0001c0001t0003g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-23+4002T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086177 | ||||||
chr10:35086184
|
GT | G | 22 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+3994delA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086184 | ||||||
chr10:35086416
|
C | T | 112 | a0001c0001t0032g0288a0001c0002t0002g0001a0001c0002t0002g0003others(109): Show | 117 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-23+3763G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086416 | ||||||
chr10:35086423
|
G | T | 1 | a0001c0001t0007g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-23+3756C>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086423 | ||||||
chr10:35086500
|
T | C | 1 | a0001c0008t0033g0106 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-23+3679A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086500 | ||||||
chr10:35086719
|
A | AAAAT | 4 | a0001c0001t0001g0026a0001c0005t0001g0229a0001c0005t0001g0230others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+3456_-23+3459d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086719 | ||||||
chr10:35086719
|
AAAATAAA others(1): Show |
A | 13 | a0001c0001t0032g0288a0001c0004t0006g0006a0001c0004t0006g0242others(10): Show | 13 | HG00738.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+3452_-23+3459d others(10): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086719 | ||||||
chr10:35086927
|
A | G | 2 | a0001c0003t0020g0176a0001c0003t0020g0177 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-23+3252T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35086927 | ||||||
chr10:35087202
|
C | A | 2 | a0001c0001t0012g0238a0001c0001t0012g0239 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+2977G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087202 | ||||||
chr10:35087262
|
T | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+2917A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087262 | ||||||
chr10:35087282
|
A | AT | 5 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(2): Show | 5 | HG00738.hp2 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+2896dupA | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087282 | ||||||
chr10:35087310
|
T | C | 2 | a0001c0001t0011g0240a0001c0001t0011g0241 | 2 | HG00621.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-23+2869A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087310 | ||||||
chr10:35087418
|
T | C | 4 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+2761A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087418 | ||||||
chr10:35087461
|
T | C | 2 | a0001c0004t0006g0289a0001c0004t0006g0290 | 2 | HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-23+2718A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087461 | ||||||
chr10:35087706
|
A | G | 5 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(2): Show | 5 | HG00738.hp2 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+2473T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087706 | ||||||
chr10:35087762
|
C | T | 100 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(97): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-23+2417G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087762 | ||||||
chr10:35087764
|
C | T | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+2415G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087764 | ||||||
chr10:35087841
|
T | C | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23+2338A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087841 | ||||||
chr10:35087872
|
T | C | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23+2307A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087872 | ||||||
chr10:35087884
|
C | CA | 284 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-23+2294dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35087884 | ||||||
chr10:35088181
|
T | A | 9 | a0001c0004t0006g0242a0001c0004t0006g0243a0001c0004t0006g0244others(6): Show | 9 | HG00738.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+1998A>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088181 | ||||||
chr10:35088275
|
TGAG | T | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1901_-23+1903d others(5): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088275 | ||||||
chr10:35088376
|
C | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+1803G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088376 | ||||||
chr10:35088429
|
A | AC | 121 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(118): Show | 126 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-23+1749dupG | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088429 | ||||||
chr10:35088429
|
A | C | 1 | a0001c0002t0002g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-23+1750T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088429 | ||||||
chr10:35088431
|
T | C | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+1748A>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088431 | ||||||
chr10:35088432
|
G | GGGAGGC | 122 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(119): Show | 127 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-23+1746_-23+1747i others(8): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088432 | ||||||
chr10:35088442
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG01258.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-23+1737T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088442 | ||||||
chr10:35088495
|
G | A | 5 | a0001c0001t0011g0246a0001c0001t0019g0215a0001c0001t0019g0216others(2): Show | 5 | HG01192.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1684C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088495 | ||||||
chr10:35088499
|
C | CA | 125 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-23+1679dupT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088499 | ||||||
chr10:35088499
|
C | CAA | 7 | a0001c0001t0001g0119a0001c0001t0001g0273a0001c0001t0003g0009others(4): Show | 7 | HG00735.hp2 HG01109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+1678_-23+1679d others(4): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088499 | ||||||
chr10:35088499
|
C | CAAAA | 58 | a0001c0001t0001g0013a0001c0002t0002g0001a0001c0002t0002g0003others(55): Show | 62 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-23+1676_-23+1679d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088499 | ||||||
chr10:35088499
|
C | CAAAAA | 13 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0002t0002g0183others(10): Show | 13 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+1675_-23+1679d others(7): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088499 | ||||||
chr10:35088499
|
CAAAA | C | 30 | a0001c0003t0005g0192a0001c0003t0005g0193a0001c0003t0005g0194others(27): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+1676_-23+1679d others(6): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088499 | ||||||
chr10:35088709
|
A | G | 3 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0220 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+1470T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088709 | ||||||
chr10:35088787
|
A | G | 101 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(98): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23+1392T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088787 | ||||||
chr10:35088849
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-23+1330G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088849 | ||||||
chr10:35088957
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-23+1222G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35088957 | ||||||
chr10:35089106
|
C | T | 2 | a0001c0003t0015g0213a0001c0003t0015g0214 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+1073G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089106 | ||||||
chr10:35089154
|
G | A | 3 | a0001c0004t0006g0006a0001c0004t0006g0289a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+1025C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089154 | ||||||
chr10:35089317
|
G | C | 1 | a0001c0003t0010g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-23+862C>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089317 | ||||||
chr10:35089426
|
G | A | 3 | a0001c0004t0006g0006a0001c0004t0006g0289a0001c0004t0006g0290 | 3 | HG01071.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+753C>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089426 | ||||||
chr10:35089731
|
A | G | 69 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(66): Show | 73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-23+448T>C | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089731 | ||||||
chr10:35089773
|
C | T | 1 | a0001c0001t0031g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-23+406G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089773 | ||||||
chr10:35089810
|
G | GC | 14 | a0001c0001t0001g0008a0001c0001t0001g0110a0001c0001t0001g0111others(11): Show | 14 | HG00642.hp2 HG02015.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+368dupG | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089810 | ||||||
chr10:35089810
|
GCC | G | 97 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0121others(94): Show | 102 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-23+367_-23+368del others(2): Show |
CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089810 | ||||||
chr10:35089818
|
C | A | 18 | a0001c0001t0007g0280a0001c0001t0007g0282a0001c0001t0007g0283others(15): Show | 18 | HG00741.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-23+361G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089818 | ||||||
chr10:35089819
|
CA | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG00741.hp1 HG01123.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+359delT | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089819 | ||||||
chr10:35089820
|
A | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-23+359T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089820 | ||||||
chr10:35089822
|
A | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0003g0009 | 3 | HG02056.hp2 HG02132.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-23+357T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089822 | ||||||
chr10:35089833
|
A | C | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+346T>G | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089833 | ||||||
chr10:35089835
|
C | A | 1 | a0001c0003t0005g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+344G>T | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089835 | ||||||
chr10:35089998
|
C | T | 1 | a0001c0004t0006g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+181G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35089998 | ||||||
chr10:35090079
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-23+100G>A | CUL2 | ENSG00000108094.17 | transcript | ENST00000374749.8 | protein_coding | 1/20 | chr10 | 35090079 |