geneid | 79677 |
---|---|
ensemblid | ENSG00000163029.16 |
hgncid | 20466 |
symbol | SMC6 |
name | structural maintenance of chromosomes 6 |
refseq_nuc | NM_001142286.2 |
refseq_prot | NP_001135758.1 |
ensembl_nuc | ENST00000448223.7 |
ensembl_prot | ENSP00000404092.2 |
mane_status | MANE Select |
chr | chr2 |
start | 17663812 |
end | 17753810 |
strand | - |
ver | v1.2 |
region | chr2:17663812-17753810 |
region5000 | chr2:17658812-17758810 |
regionname0 | SMC6_chr2_17663812_17753810 |
regionname5000 | SMC6_chr2_17658812_17758810 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1091 | 193 | 52 | 42 | 69 | 9 | 20 | 48 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0002 | 0/0 | 1091 | 32 | 24 | 4 | 0 | 2 | 2 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0003 | 0/1 | 1091 | 28 | 6 | 12 | 4 | 3 | 2 | 4 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0004 | 0/0 | 1091 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3276 | 190 | 51 | 41 | 68 | 9 | 20 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0002 | 0/1 | 3276 | 28 | 6 | 12 | 4 | 3 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0003 | 0/0 | 3276 | 26 | 19 | 3 | 0 | 2 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0004 | 0/0 | 3276 | 6 | 5 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0005 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0006 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0007 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
c0008 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1965 | 73 | 44 | 16 | 3 | 5 | 4 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0002 | 0/0 | 1965 | 69 | 22 | 18 | 10 | 6 | 13 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0003 | 1/0 | 1965 | 64 | 2 | 18 | 36 | 2 | 5 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0004 | 0/0 | 1964 | 22 | 5 | 1 | 16 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0005 | 0/0 | 1964 | 10 | 4 | 0 | 4 | 1 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0006 | 0/0 | 1965 | 2 | 1 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0007 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0008 | 0/0 | 1965 | 2 | 0 | 1 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0009 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0010 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0011 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0012 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0013 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0014 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0015 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0016 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
t0017 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3276 | 190 | 51 | 41 | 68 | 9 | 20 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0005 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0006 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0007 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0002c0003 | 0/0 | 3276 | 26 | 19 | 3 | 0 | 2 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0002c0004 | 0/0 | 3276 | 6 | 5 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0003c0002 | 0/1 | 3276 | 28 | 6 | 12 | 4 | 3 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0004c0008 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5240 | 21 | 20 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0002 | 0/0 | 5240 | 63 | 17 | 17 | 10 | 6 | 13 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0003 | 1/0 | 5240 | 63 | 2 | 18 | 35 | 2 | 5 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0004 | 0/0 | 5239 | 22 | 5 | 1 | 16 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0005 | 0/0 | 5239 | 10 | 4 | 0 | 4 | 1 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0006 | 0/0 | 5240 | 2 | 1 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0007 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0008 | 0/0 | 5240 | 2 | 0 | 1 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0013 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0014 | 0/0 | 5240 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0015 | 0/0 | 5240 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0016 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0001t0017 | 0/0 | 5239 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0005t0001 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0006t0010 | 0/0 | 5240 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0001c0007t0003 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0002c0003t0001 | 0/0 | 5240 | 26 | 19 | 3 | 0 | 2 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0002c0004t0002 | 0/0 | 5240 | 6 | 5 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0003c0002t0001 | 0/1 | 5240 | 25 | 4 | 12 | 3 | 3 | 2 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0003c0002t0009 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0003c0002t0011 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
a0004c0008t0012 | 0/0 | 5239 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | copy fasta | chr2 | 17658812 | 17758810 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0014g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0015g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0016g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0006t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0001c0007t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0002c0004t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0003c0002t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
a0004c0008t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | GBR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | GBR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | GBR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00140 | hp2 | a0003 | c0002 | t0001 | g0200 | EUR | GBR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0008 | EUR | FIN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00323 | hp1 | a0003 | c0002 | t0001 | g0166 | EUR | FIN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | FIN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00642 | hp1 | a0001 | c0001 | t0014 | g0050 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00735 | hp2 | a0003 | c0002 | t0001 | g0191 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00738 | hp2 | a0003 | c0002 | t0001 | g0168 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01069 | hp1 | a0001 | c0006 | t0010 | g0010 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01099 | hp2 | a0002 | c0004 | t0002 | g0188 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01109 | hp1 | a0003 | c0002 | t0001 | g0190 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0164 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01175 | hp2 | a0003 | c0002 | t0001 | g0201 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01192 | hp2 | a0003 | c0002 | t0001 | g0167 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01256 | hp1 | a0003 | c0002 | t0001 | g0163 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01258 | hp1 | a0002 | c0003 | t0001 | g0165 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01258 | hp2 | a0003 | c0002 | t0001 | g0162 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01261 | hp1 | a0001 | c0001 | t0015 | g0014 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01358 | hp1 | a0003 | c0002 | t0001 | g0158 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01433 | hp1 | a0003 | c0002 | t0001 | g0193 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0216 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01516 | hp1 | a0003 | c0002 | t0001 | g0192 | EUR | IBS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0152 | EUR | IBS | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01891 | hp1 | a0002 | c0003 | t0001 | g0177 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01981 | hp1 | a0003 | c0002 | t0001 | g0009 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02004 | hp2 | a0003 | c0002 | t0001 | g0009 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02055 | hp1 | a0002 | c0004 | t0002 | g0183 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CDX | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0155 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0154 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02300 | hp2 | a0003 | c0002 | t0001 | g0189 | AMR | PEL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02615 | hp1 | a0002 | c0003 | t0001 | g0137 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0135 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0133 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02717 | hp1 | a0003 | c0002 | t0001 | g0180 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0144 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02723 | hp2 | a0003 | c0002 | t0001 | g0160 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0134 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0150 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0156 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0153 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02970 | hp2 | a0002 | c0004 | t0002 | g0184 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0151 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0172 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03041 | hp2 | a0002 | c0004 | t0002 | g0179 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03098 | hp2 | a0003 | c0002 | t0009 | g0232 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03139 | hp2 | a0002 | c0004 | t0002 | g0185 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0169 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03453 | hp1 | a0002 | c0003 | t0001 | g0182 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03516 | hp1 | a0002 | c0004 | t0002 | g0186 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03579 | hp1 | a0003 | c0002 | t0001 | g0161 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03654 | hp2 | a0003 | c0002 | t0001 | g0196 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0215 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | BEB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0170 | SAS | BEB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | BEB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04228 | hp1 | a0003 | c0002 | t0001 | g0178 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | STU | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0181 | AFR | YRI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18747 | hp1 | a0004 | c0008 | t0012 | g0195 | EAS | CHB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18747 | hp2 | a0001 | c0001 | t0013 | g0106 | EAS | CHB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | YRI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18953 | hp1 | a0001 | c0001 | t0016 | g0138 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18978 | hp1 | a0001 | c0001 | t0017 | g0244 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18978 | hp2 | a0001 | c0007 | t0003 | g0112 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | LWK | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | LWK | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19057 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19067 | hp2 | a0003 | c0002 | t0011 | g0197 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA19077 | hp2 | a0003 | c0002 | t0001 | g0199 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ASW | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0136 | AFR | ASW | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0243 | EUR | TSI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | TSI | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | GIH | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | GIH | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02559 | hp1 | a0003 | c0002 | t0001 | g0173 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG02559 | hp2 | a0002 | c0003 | t0001 | g0145 | AFR | ACB | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03471 | hp1 | a0003 | c0002 | t0009 | g0233 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | USA | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | USA | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
NA18955 | hp2 | a0003 | c0002 | t0001 | g0198 | EAS | JPT | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
homoSapiens_chm13v2 | hp1 | a0003 | c0002 | t0001 | g0157 | REF | REF | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0062 | REF | REF | SMC6_chr2_17658812_17758810 | SMC6 | chr2 | 17658812 | 17758810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17703228
|
C | T | 2 | a0002a0003 | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
missense_variant | MODERATE | c.2071G>A | p.Ala691Thr | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/28 | 2348/5240 | 2071/3276 | 691/1091 | chr2 | 17703228 | ||
chr2:17716221
|
T | C | 2 | a0003a0004 | 29 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(26): Show |
missense_variant | MODERATE | c.1390A>G | p.Arg464Gly | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/28 | 1667/5240 | 1390/3276 | 464/1091 | chr2 | 17716221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17683727
|
C | A | 1 | a0001c0007 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.2715G>T | p.Leu905Leu | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/28 | 2992/5240 | 2715/3276 | 905/1091 | chr2 | 17683727 | ||
chr2:17708651
|
C | T | 1 | a0002c0004 | 6 | HG01099.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.1833G>A | p.Val611Val | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/28 | 2110/5240 | 1833/3276 | 611/1091 | chr2 | 17708651 | ||
chr2:17714989
|
A | G | 1 | a0001c0006 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.1602T>C | p.Tyr534Tyr | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/28 | 1879/5240 | 1602/3276 | 534/1091 | chr2 | 17714989 | ||
chr2:17721223
|
C | T | 1 | a0001c0005 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.765G>A | p.Glu255Glu | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 10/28 | 1042/5240 | 765/3276 | 255/1091 | chr2 | 17721223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17663864
|
C | A | 1 | a0001c0001t0014 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 1635 | chr2 | 17663864 | |||||
chr2:17663915
|
T | C | 1 | a0001c0001t0008 | 2 | HG01433.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 1584 | chr2 | 17663915 | |||||
chr2:17664029
|
A | G | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1470T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 1470 | chr2 | 17664029 | |||||
chr2:17664055
|
A | C | 1 | a0003c0002t0011 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1444T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 1444 | chr2 | 17664055 | |||||
chr2:17664739
|
TG | T | 3 | a0001c0001t0005a0001c0001t0017a0004c0008t0012 | 12 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*759delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 759 | chr2 | 17664739 | |||||
chr2:17664895
|
A | G | 7 | a0001c0001t0001a0001c0001t0007a0001c0005t0001others(4): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*604T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 604 | chr2 | 17664895 | |||||
chr2:17664910
|
G | A | 1 | a0001c0001t0017 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 589 | chr2 | 17664910 | |||||
chr2:17664981
|
A | C | 1 | a0001c0006t0010 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 518 | chr2 | 17664981 | |||||
chr2:17664987
|
AG | A | 1 | a0001c0001t0004 | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*511delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 511 | chr2 | 17664987 | |||||
chr2:17665246
|
C | T | 1 | a0001c0001t0007 | 2 | HG02572.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*253G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 253 | chr2 | 17665246 | |||||
chr2:17665325
|
A | T | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*174T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 174 | chr2 | 17665325 | |||||
chr2:17665493
|
T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 28/28 | 6 | chr2 | 17665493 | |||||
chr2:17752989
|
T | C | 1 | a0001c0001t0016 | 1 | NA18953.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/28 | 7043 | chr2 | 17752989 | |||||
chr2:17753052
|
C | T | 1 | a0001c0001t0006 | 2 | HG01255.hp2 HG02572.hp1 |
5_prime_UTR_variant | MODIFIER | c.-80G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/28 | 7106 | chr2 | 17753052 | |||||
chr2:17753769
|
G | C | 1 | a0003c0002t0009 | 2 | HG03098.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-236C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/28 | 7823 | chr2 | 17753769 | |||||
chr2:17753771
|
T | C | 2 | a0001c0001t0005a0001c0001t0017 | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-238A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/28 | chr2 | 17753771 | ||||||
chr2:17753788
|
C | G | 1 | a0001c0006t0010 | 1 | HG01069.hp1 | 5_prime_UTR_variant | MODIFIER | c.-255G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/28 | 7842 | chr2 | 17753788 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17666023
|
A | G | 1 | a0001c0001t0005g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3161+397T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 27/27 | chr2 | 17666023 | ||||||
chr2:17666200
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3161+220A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 27/27 | chr2 | 17666200 | ||||||
chr2:17666368
|
C | A | 1 | a0002c0003t0001g0177 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3161+52G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 27/27 | chr2 | 17666368 | ||||||
chr2:17666539
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3064-22A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17666539 | ||||||
chr2:17666820
|
CA | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3064-304delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17666820 | ||||||
chr2:17666866
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3064-349A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17666866 | ||||||
chr2:17666922
|
T | C | 43 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(40): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.3064-405A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17666922 | ||||||
chr2:17667287
|
TACCATTT others(29): Show |
T | 1 | a0003c0002t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3064-806_3064-771d others(38): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17667287 | ||||||
chr2:17667345
|
T | C | 23 | a0001c0001t0001g0147a0001c0001t0004g0003a0001c0001t0004g0022others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.3064-828A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17667345 | ||||||
chr2:17667588
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3064-1071C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17667588 | ||||||
chr2:17667692
|
A | G | 44 | a0001c0001t0001g0171a0002c0003t0001g0007a0002c0003t0001g0008others(41): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.3064-1175T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17667692 | ||||||
chr2:17668001
|
CTG | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.3064-1486_3064-148 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17668001 | ||||||
chr2:17668400
|
C | T | 30 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(27): Show | 32 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.3064-1883G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17668400 | ||||||
chr2:17668766
|
C | T | 7 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(4): Show | 7 | HG01261.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3063+1657G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17668766 | ||||||
chr2:17668808
|
A | G | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3063+1615T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17668808 | ||||||
chr2:17668823
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3063+1600C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17668823 | ||||||
chr2:17669263
|
G | A | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3063+1160C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17669263 | ||||||
chr2:17669274
|
A | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3063+1149T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17669274 | ||||||
chr2:17669509
|
C | A | 1 | a0001c0001t0003g0114 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3063+914G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17669509 | ||||||
chr2:17669577
|
G | A | 6 | a0001c0001t0003g0046a0001c0001t0003g0051a0001c0001t0003g0054others(3): Show | 6 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.3063+846C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17669577 | ||||||
chr2:17669974
|
A | G | 13 | a0003c0002t0001g0009a0003c0002t0001g0189a0003c0002t0001g0190others(10): Show | 14 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3063+449T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17669974 | ||||||
chr2:17670230
|
G | A | 1 | a0001c0001t0013g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3063+193C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 26/27 | chr2 | 17670230 | ||||||
chr2:17670752
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2911-177C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17670752 | ||||||
chr2:17670791
|
C | A | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2911-216G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17670791 | ||||||
chr2:17670963
|
G | T | 1 | a0001c0001t0004g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2911-388C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17670963 | ||||||
chr2:17670990
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2911-415A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17670990 | ||||||
chr2:17671010
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2911-435A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671010 | ||||||
chr2:17671036
|
G | GT | 46 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(43): Show | 49 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2911-462dupA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671036 | ||||||
chr2:17671038
|
T | G | 1 | a0002c0003t0001g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2911-463A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671038 | ||||||
chr2:17671082
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2911-507G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671082 | ||||||
chr2:17671243
|
T | C | 12 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(9): Show | 12 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2911-668A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671243 | ||||||
chr2:17671269
|
C | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0099 | 2 | HG00423.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2911-694G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671269 | ||||||
chr2:17671274
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2911-699G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671274 | ||||||
chr2:17671380
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2911-805C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671380 | ||||||
chr2:17671383
|
AC | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(240): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2911-809delG | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671383 | ||||||
chr2:17671431
|
C | CCA | 49 | a0001c0001t0003g0053a0001c0001t0003g0057a0002c0003t0001g0007others(46): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2911-858_2911-857d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671431 | ||||||
chr2:17671431
|
C | CCACA | 2 | a0003c0002t0001g0009a0003c0002t0001g0190 | 3 | HG01109.hp1 HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2911-860_2911-857d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671431 | ||||||
chr2:17671463
|
G | A | 1 | a0001c0001t0003g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2911-888C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671463 | ||||||
chr2:17671470
|
A | T | 19 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(16): Show | 19 | HG00140.hp1 HG01069.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2911-895T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671470 | ||||||
chr2:17671508
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0210 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2911-933G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671508 | ||||||
chr2:17671570
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2911-995A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671570 | ||||||
chr2:17671608
|
C | CAA | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2911-1035_2911-103 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671608 | ||||||
chr2:17671608
|
CA | C | 75 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0111others(72): Show | 75 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.2911-1034delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671608 | ||||||
chr2:17671608
|
CAA | C | 71 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0002g0005others(68): Show | 72 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.2911-1035_2911-103 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671608 | ||||||
chr2:17671608
|
CAAA | C | 78 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(75): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2911-1036_2911-103 others(7): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671608 | ||||||
chr2:17671644
|
A | G | 2 | a0001c0001t0005g0235a0001c0001t0005g0239 | 2 | NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2911-1069T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671644 | ||||||
chr2:17671805
|
A | G | 2 | a0001c0001t0003g0072a0001c0001t0003g0075 | 2 | NA18979.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2911-1230T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671805 | ||||||
chr2:17671990
|
CATTT | C | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2911-1419_2911-141 others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17671990 | ||||||
chr2:17672049
|
A | T | 2 | a0003c0002t0001g0194a0003c0002t0001g0199 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2911-1474T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672049 | ||||||
chr2:17672121
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(172): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2911-1546A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672121 | ||||||
chr2:17672421
|
T | TCC | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(240): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2911-1847_2911-184 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672421 | ||||||
chr2:17672426
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0002c0003t0001g0133others(6): Show | 9 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2911-1851A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672426 | ||||||
chr2:17672555
|
T | C | 42 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(39): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.2911-1980A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672555 | ||||||
chr2:17672633
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2911-2058T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672633 | ||||||
chr2:17672851
|
T | G | 48 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0045others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2911-2276A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17672851 | ||||||
chr2:17673169
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2911-2594G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673169 | ||||||
chr2:17673260
|
T | A | 1 | a0001c0001t0003g0044 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2911-2685A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673260 | ||||||
chr2:17673554
|
A | T | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2911-2979T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673554 | ||||||
chr2:17673561
|
A | T | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2911-2986T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673561 | ||||||
chr2:17673561
|
AATTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2911-2998_2911-298 others(16): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673561 | ||||||
chr2:17673562
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2911-2987T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673562 | ||||||
chr2:17673574
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2911-2999T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673574 | ||||||
chr2:17673624
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(119): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2911-3049A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673624 | ||||||
chr2:17673638
|
C | T | 2 | a0001c0001t0003g0053a0001c0001t0003g0057 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.2911-3063G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673638 | ||||||
chr2:17673655
|
C | T | 9 | a0001c0001t0005g0235a0001c0001t0005g0236a0001c0001t0005g0237others(6): Show | 9 | HG02056.hp1 HG02145.hp1 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.2911-3080G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673655 | ||||||
chr2:17673672
|
C | T | 20 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(17): Show | 21 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2911-3097G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673672 | ||||||
chr2:17673837
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2911-3262C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673837 | ||||||
chr2:17673875
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2911-3300A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673875 | ||||||
chr2:17673958
|
G | A | 2 | a0001c0001t0004g0033a0001c0001t0004g0036 | 2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2911-3383C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17673958 | ||||||
chr2:17674036
|
T | G | 1 | a0001c0001t0003g0098 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2911-3461A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17674036 | ||||||
chr2:17674110
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2911-3535T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17674110 | ||||||
chr2:17674269
|
T | C | 1 | a0001c0001t0003g0046 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2911-3694A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17674269 | ||||||
chr2:17674396
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2911-3821A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17674396 | ||||||
chr2:17675134
|
GTC | G | 6 | a0002c0003t0001g0008a0002c0003t0001g0152a0002c0003t0001g0164others(3): Show | 7 | HG00280.hp2 HG01168.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2910+3723_2910+372 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675134 | ||||||
chr2:17675239
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2910+3620A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675239 | ||||||
chr2:17675322
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2910+3537T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675322 | ||||||
chr2:17675604
|
T | C | 12 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(9): Show | 12 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2910+3255A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675604 | ||||||
chr2:17675963
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.2910+2896G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675963 | ||||||
chr2:17675968
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2910+2891G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17675968 | ||||||
chr2:17676116
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2910+2743A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676116 | ||||||
chr2:17676374
|
T | C | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2910+2485A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676374 | ||||||
chr2:17676495
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2910+2364A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676495 | ||||||
chr2:17676506
|
A | C | 1 | a0001c0001t0006g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2910+2353T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676506 | ||||||
chr2:17676555
|
G | A | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2910+2304C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676555 | ||||||
chr2:17676574
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2910+2285A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676574 | ||||||
chr2:17676680
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2910+2179T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676680 | ||||||
chr2:17676795
|
T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2910+2064A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676795 | ||||||
chr2:17676908
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2910+1951G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676908 | ||||||
chr2:17676926
|
A | G | 2 | a0001c0001t0005g0238a0001c0001t0005g0241 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2910+1933T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17676926 | ||||||
chr2:17677030
|
C | CT | 23 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2910+1828dupA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677030 | ||||||
chr2:17677176
|
G | T | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2910+1683C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677176 | ||||||
chr2:17677202
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(89): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2910+1657C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677202 | ||||||
chr2:17677447
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(89): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2910+1412C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677447 | ||||||
chr2:17677871
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2910+988A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677871 | ||||||
chr2:17677990
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2910+869C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17677990 | ||||||
chr2:17678108
|
A | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2910+751T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17678108 | ||||||
chr2:17678388
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.2910+471G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17678388 | ||||||
chr2:17678606
|
G | GA | 58 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(55): Show | 60 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.2910+252dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17678606 | ||||||
chr2:17678730
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2910+129A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 25/27 | chr2 | 17678730 | ||||||
chr2:17679539
|
T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2805-575A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17679539 | ||||||
chr2:17679689
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2805-725G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17679689 | ||||||
chr2:17679691
|
C | T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2805-727G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17679691 | ||||||
chr2:17679716
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2805-752G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17679716 | ||||||
chr2:17679998
|
G | A | 1 | a0002c0003t0001g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2805-1034C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17679998 | ||||||
chr2:17680103
|
G | C | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2805-1139C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17680103 | ||||||
chr2:17680161
|
A | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2805-1197T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17680161 | ||||||
chr2:17680486
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.2805-1522T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17680486 | ||||||
chr2:17680825
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2805-1861T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17680825 | ||||||
chr2:17681503
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2804+2135A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681503 | ||||||
chr2:17681546
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2804+2092A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681546 | ||||||
chr2:17681564
|
C | A | 1 | a0001c0001t0002g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2804+2074G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681564 | ||||||
chr2:17681699
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2804+1939C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681699 | ||||||
chr2:17681842
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2804+1796A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681842 | ||||||
chr2:17681920
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2804+1718A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17681920 | ||||||
chr2:17682324
|
A | G | 1 | a0001c0001t0003g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2804+1314T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682324 | ||||||
chr2:17682427
|
C | G | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2804+1211G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682427 | ||||||
chr2:17682727
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2804+911C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682727 | ||||||
chr2:17682735
|
T | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2804+903A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682735 | ||||||
chr2:17682760
|
TA | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2804+877delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682760 | ||||||
chr2:17682883
|
CT | C | 117 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(114): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2804+754delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682883 | ||||||
chr2:17682885
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2804+753A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17682885 | ||||||
chr2:17683014
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2804+624C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683014 | ||||||
chr2:17683036
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | HG00639.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2804+602G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683036 | ||||||
chr2:17683288
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2804+350A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683288 | ||||||
chr2:17683381
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2804+257C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683381 | ||||||
chr2:17683413
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2804+225T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683413 | ||||||
chr2:17683508
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2804+130T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 24/27 | chr2 | 17683508 | ||||||
chr2:17683904
|
T | A | 1 | a0002c0003t0001g0165 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2679-141A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17683904 | ||||||
chr2:17684048
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2679-285C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684048 | ||||||
chr2:17684061
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2679-298T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684061 | ||||||
chr2:17684175
|
C | T | 1 | a0003c0002t0001g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2679-412G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684175 | ||||||
chr2:17684649
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2679-886A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684649 | ||||||
chr2:17684887
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2679-1124A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684887 | ||||||
chr2:17684983
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2679-1220G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17684983 | ||||||
chr2:17685088
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2679-1325C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685088 | ||||||
chr2:17685128
|
G | GAA | 142 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(139): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2679-1367_2679-136 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685128 | ||||||
chr2:17685312
|
A | C | 6 | a0002c0004t0002g0179a0002c0004t0002g0183a0002c0004t0002g0184others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2679-1549T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685312 | ||||||
chr2:17685386
|
CTCA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2679-1626_2679-162 others(7): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685386 | ||||||
chr2:17685406
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2679-1643C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685406 | ||||||
chr2:17685500
|
C | T | 4 | a0001c0001t0002g0120a0001c0001t0002g0123a0001c0001t0002g0129others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2679-1737G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685500 | ||||||
chr2:17685638
|
T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2679-1875A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685638 | ||||||
chr2:17685848
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2679-2085A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17685848 | ||||||
chr2:17686157
|
A | G | 1 | a0001c0001t0005g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2679-2394T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686157 | ||||||
chr2:17686176
|
T | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2679-2413A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686176 | ||||||
chr2:17686204
|
G | A | 2 | a0001c0001t0005g0238a0001c0001t0005g0241 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2679-2441C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686204 | ||||||
chr2:17686242
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679-2479C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686242 | ||||||
chr2:17686560
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2679-2797C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686560 | ||||||
chr2:17686738
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2679-2975G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686738 | ||||||
chr2:17686802
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0037others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2679-3039C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686802 | ||||||
chr2:17686869
|
G | T | 48 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0045others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2679-3106C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17686869 | ||||||
chr2:17687007
|
G | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2679-3244C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17687007 | ||||||
chr2:17687028
|
T | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2679-3265A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17687028 | ||||||
chr2:17687492
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.2679-3729G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17687492 | ||||||
chr2:17687527
|
AAGT | A | 56 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0133others(53): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2679-3767_2679-376 others(7): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17687527 | ||||||
chr2:17688046
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2679-4283C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688046 | ||||||
chr2:17688075
|
T | C | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2679-4312A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688075 | ||||||
chr2:17688133
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2679-4370C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688133 | ||||||
chr2:17688270
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2679-4507A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688270 | ||||||
chr2:17688315
|
T | TA | 41 | a0001c0001t0001g0171a0001c0001t0002g0174a0001c0001t0002g0175others(38): Show | 41 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.2679-4553dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688315 | ||||||
chr2:17688315
|
T | TAA | 6 | a0001c0001t0002g0187a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG00140.hp1 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2679-4554_2679-455 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688315 | ||||||
chr2:17688315
|
TA | T | 6 | a0001c0001t0001g0139a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG01099.hp1 HG01168.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2679-4553delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688315 | ||||||
chr2:17688479
|
C | G | 1 | a0001c0001t0003g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2679-4716G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688479 | ||||||
chr2:17688552
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2679-4789C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17688552 | ||||||
chr2:17689061
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2679-5298C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689061 | ||||||
chr2:17689093
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2679-5330G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689093 | ||||||
chr2:17689365
|
C | T | 1 | a0003c0002t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2679-5602G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689365 | ||||||
chr2:17689459
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2678+5693C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689459 | ||||||
chr2:17689507
|
C | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2678+5645G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689507 | ||||||
chr2:17689691
|
C | T | 1 | a0001c0001t0017g0244 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2678+5461G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689691 | ||||||
chr2:17689855
|
A | C | 2 | a0003c0002t0001g0200a0003c0002t0001g0201 | 2 | HG00140.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2678+5297T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689855 | ||||||
chr2:17689986
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2678+5166A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689986 | ||||||
chr2:17689993
|
C | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2678+5159G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17689993 | ||||||
chr2:17690435
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.2678+4717C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690435 | ||||||
chr2:17690630
|
AC | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2678+4521delG | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690630 | ||||||
chr2:17690720
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2678+4432A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690720 | ||||||
chr2:17690757
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2678+4395G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690757 | ||||||
chr2:17690783
|
A | G | 1 | a0001c0001t0006g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2678+4369T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690783 | ||||||
chr2:17690938
|
C | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(3): Show | 7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2678+4214G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17690938 | ||||||
chr2:17691017
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+4135A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691017 | ||||||
chr2:17691027
|
A | G | 1 | a0001c0001t0004g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2678+4125T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691027 | ||||||
chr2:17691233
|
T | TAC | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.2678+3917_2678+391 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691233
|
TAC | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 75 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.2678+3917_2678+391 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691233
|
TACAC | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0066a0003c0002t0001g0200others(1): Show | 5 | HG00140.hp2 HG01175.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2678+3915_2678+391 others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691233
|
TACACAC | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2678+3913_2678+391 others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691233
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(1): Show | 4 | HG00099.hp1 HG01256.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2678+3909_2678+391 others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691233
|
TACACACA others(5): Show |
T | 1 | a0003c0002t0001g0194 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2678+3907_2678+391 others(16): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691233 | ||||||
chr2:17691249
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2678+3903G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691249 | ||||||
chr2:17691251
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2678+3901G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691251 | ||||||
chr2:17691274
|
C | A | 1 | a0001c0001t0002g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2678+3878G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691274 | ||||||
chr2:17691313
|
G | GGT | 3 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147 | 4 | HG02717.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2678+3837_2678+383 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691313 | ||||||
chr2:17691313
|
GGT | G | 3 | a0001c0001t0002g0125a0001c0001t0005g0238a0002c0003t0001g0150 | 3 | HG01081.hp2 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2678+3837_2678+383 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691313 | ||||||
chr2:17691342
|
G | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+3810C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691342 | ||||||
chr2:17691344
|
G | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+3808C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691344 | ||||||
chr2:17691350
|
C | CTG | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2678+3800_2678+380 others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691350 | ||||||
chr2:17691350
|
C | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+3802G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691350 | ||||||
chr2:17691350
|
CTGTGTGT others(1): Show |
C | 119 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2678+3794_2678+380 others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691350 | ||||||
chr2:17691358
|
G | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+3794C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691358 | ||||||
chr2:17691397
|
T | C | 1 | a0003c0002t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2678+3755A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691397 | ||||||
chr2:17691444
|
G | T | 12 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(9): Show | 12 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2678+3708C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691444 | ||||||
chr2:17691459
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2678+3692delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691459 | ||||||
chr2:17691769
|
C | T | 1 | a0002c0003t0001g0181 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2678+3383G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691769 | ||||||
chr2:17691773
|
T | C | 1 | a0001c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2678+3379A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691773 | ||||||
chr2:17691800
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2678+3352T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691800 | ||||||
chr2:17691862
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0037others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2678+3290T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691862 | ||||||
chr2:17691881
|
C | T | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2678+3271G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691881 | ||||||
chr2:17691944
|
T | C | 9 | a0001c0001t0005g0235a0001c0001t0005g0236a0001c0001t0005g0237others(6): Show | 9 | HG02056.hp1 HG02145.hp1 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.2678+3208A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17691944 | ||||||
chr2:17692059
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2678+3093A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692059 | ||||||
chr2:17692086
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2678+3066G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692086 | ||||||
chr2:17692124
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(123): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.2678+3028G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692124 | ||||||
chr2:17692127
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2678+3025A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692127 | ||||||
chr2:17692154
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2678+2998G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692154 | ||||||
chr2:17692201
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2678+2951C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692201 | ||||||
chr2:17692217
|
T | C | 2 | a0003c0002t0001g0160a0003c0002t0001g0161 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2678+2935A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692217 | ||||||
chr2:17692220
|
G | A | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2678+2932C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692220 | ||||||
chr2:17692401
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2678+2751C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692401 | ||||||
chr2:17692455
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2678+2697C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692455 | ||||||
chr2:17692494
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2678+2658C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692494 | ||||||
chr2:17692636
|
T | C | 1 | a0001c0001t0003g0102 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2678+2516A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692636 | ||||||
chr2:17692809
|
G | C | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+2343C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692809 | ||||||
chr2:17692891
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2678+2261G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692891 | ||||||
chr2:17692896
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2678+2256C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692896 | ||||||
chr2:17692910
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2678+2242G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692910 | ||||||
chr2:17692944
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2678+2208G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17692944 | ||||||
chr2:17693056
|
T | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2678+2096A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693056 | ||||||
chr2:17693192
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2678+1960G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693192 | ||||||
chr2:17693265
|
G | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0104a0001c0001t0002g0111others(3): Show | 7 | HG00408.hp2 HG00438.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+1887C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693265 | ||||||
chr2:17693311
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2678+1841A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693311 | ||||||
chr2:17693378
|
A | C | 1 | a0001c0001t0017g0244 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2678+1774T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693378 | ||||||
chr2:17693424
|
T | C | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0225 | 3 | HG01891.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2678+1728A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693424 | ||||||
chr2:17693439
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2678+1713T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693439 | ||||||
chr2:17693469
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2678+1683G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693469 | ||||||
chr2:17693473
|
C | T | 2 | a0001c0001t0008g0215a0001c0001t0008g0216 | 2 | HG01433.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2678+1679G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693473 | ||||||
chr2:17693956
|
C | T | 34 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.2678+1196G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693956 | ||||||
chr2:17693957
|
G | A | 2 | a0001c0001t0002g0120a0001c0001t0002g0123 | 2 | HG00280.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.2678+1195C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17693957 | ||||||
chr2:17694000
|
C | CA | 13 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0002g0013others(10): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.2678+1151dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694000 | ||||||
chr2:17694000
|
CA | C | 20 | a0001c0001t0002g0085a0001c0001t0004g0003a0001c0001t0004g0023others(17): Show | 21 | HG00639.hp1 HG01168.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2678+1151delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694000 | ||||||
chr2:17694020
|
AAAAAG | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(56): Show | 61 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.2678+1127_2678+113 others(9): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694020 | ||||||
chr2:17694021
|
AAAAG | A | 51 | a0001c0001t0001g0148a0001c0001t0002g0217a0001c0001t0005g0241others(48): Show | 54 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.2678+1127_2678+113 others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694021 | ||||||
chr2:17694022
|
AAAG | A | 5 | a0001c0006t0010g0010a0002c0003t0001g0155a0002c0004t0002g0183others(2): Show | 5 | HG01069.hp1 HG01175.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2678+1127_2678+112 others(7): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694022 | ||||||
chr2:17694206
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2678+946C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694206 | ||||||
chr2:17694456
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2678+696T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694456 | ||||||
chr2:17694537
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2678+615A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694537 | ||||||
chr2:17694570
|
T | C | 43 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(40): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.2678+582A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694570 | ||||||
chr2:17694693
|
A | G | 16 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(13): Show | 17 | HG00621.hp1 HG00639.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.2678+459T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694693 | ||||||
chr2:17694735
|
A | G | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+417T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694735 | ||||||
chr2:17694736
|
G | T | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+416C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694736 | ||||||
chr2:17694737
|
A | T | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+415T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694737 | ||||||
chr2:17694738
|
G | T | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+414C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694738 | ||||||
chr2:17694739
|
C | T | 46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+413G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694739 | ||||||
chr2:17694741
|
T | TACTGATT others(5): Show |
46 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2678+410_2678+411i others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694741 | ||||||
chr2:17694924
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2678+228C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694924 | ||||||
chr2:17694984
|
AG | A | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+167delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694984 | ||||||
chr2:17694986
|
G | C | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+166C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694986 | ||||||
chr2:17694988
|
T | A | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+164A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694988 | ||||||
chr2:17694989
|
A | T | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+163T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694989 | ||||||
chr2:17694992
|
A | T | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+160T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694992 | ||||||
chr2:17694994
|
T | A | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+158A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694994 | ||||||
chr2:17694997
|
T | TG | 7 | a0001c0001t0003g0044a0001c0001t0003g0071a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp1 HG01081.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2678+154_2678+155i others(3): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 23/27 | chr2 | 17694997 | ||||||
chr2:17695442
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2533-145A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 22/27 | chr2 | 17695442 | ||||||
chr2:17695596
|
C | T | 1 | a0003c0002t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2533-299G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 22/27 | chr2 | 17695596 | ||||||
chr2:17695813
|
T | C | 8 | a0003c0002t0001g0157a0003c0002t0001g0158a0003c0002t0001g0162others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2532+476A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 22/27 | chr2 | 17695813 | ||||||
chr2:17695838
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(69): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2532+451A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 22/27 | chr2 | 17695838 | ||||||
chr2:17695855
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2532+434A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 22/27 | chr2 | 17695855 | ||||||
chr2:17696506
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2395-80T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696506 | ||||||
chr2:17696547
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2395-121T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696547 | ||||||
chr2:17696611
|
AT | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2395-186delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696611 | ||||||
chr2:17696676
|
T | G | 1 | a0001c0001t0003g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2395-250A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696676 | ||||||
chr2:17696780
|
G | C | 2 | a0003c0002t0001g0009a0003c0002t0001g0190 | 3 | HG01109.hp1 HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2395-354C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696780 | ||||||
chr2:17696787
|
AG | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2395-362delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696787 | ||||||
chr2:17696945
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2395-519C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696945 | ||||||
chr2:17696977
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2395-551C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17696977 | ||||||
chr2:17697066
|
C | T | 2 | a0002c0003t0001g0144a0002c0003t0001g0145 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2395-640G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697066 | ||||||
chr2:17697279
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2395-853C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697279 | ||||||
chr2:17697342
|
A | C | 1 | a0001c0001t0003g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2395-916T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697342 | ||||||
chr2:17697686
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2395-1260C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697686 | ||||||
chr2:17697687
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2395-1261G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697687 | ||||||
chr2:17697805
|
G | A | 49 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(46): Show | 52 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2395-1379C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697805 | ||||||
chr2:17697876
|
T | C | 3 | a0001c0001t0002g0081a0001c0001t0002g0088a0001c0001t0002g0092 | 3 | HG02074.hp2 HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2395-1450A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697876 | ||||||
chr2:17697969
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2395-1543C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17697969 | ||||||
chr2:17698144
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2395-1718A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698144 | ||||||
chr2:17698289
|
A | T | 46 | a0001c0001t0001g0171a0001c0001t0002g0174a0001c0001t0002g0175others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2395-1863T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698289 | ||||||
chr2:17698636
|
A | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2394+1572T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698636 | ||||||
chr2:17698667
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2394+1541A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698667 | ||||||
chr2:17698742
|
T | C | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2394+1466A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698742 | ||||||
chr2:17698830
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+1378C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698830 | ||||||
chr2:17698831
|
T | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+1377A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698831 | ||||||
chr2:17698852
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2394+1356A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17698852 | ||||||
chr2:17699047
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2394+1161G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699047 | ||||||
chr2:17699263
|
C | T | 1 | a0001c0001t0006g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2394+945G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699263 | ||||||
chr2:17699328
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2394+880T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699328 | ||||||
chr2:17699392
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2394+816C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699392 | ||||||
chr2:17699453
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+755G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699453 | ||||||
chr2:17699688
|
G | GGATATTG others(1): Show |
21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+519_2394+520i others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699688 | ||||||
chr2:17699694
|
A | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+514T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699694 | ||||||
chr2:17699695
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+513G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699695 | ||||||
chr2:17699697
|
A | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2394+511T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699697 | ||||||
chr2:17699726
|
A | G | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2394+482T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699726 | ||||||
chr2:17699731
|
G | A | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2394+477C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699731 | ||||||
chr2:17699886
|
C | A | 1 | a0001c0001t0005g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2394+322G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699886 | ||||||
chr2:17699916
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2394+292G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17699916 | ||||||
chr2:17700182
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2394+26G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 21/27 | chr2 | 17700182 | ||||||
chr2:17700504
|
T | TAGAA | 23 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.2224-130_2224-127d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17700504 | ||||||
chr2:17700514
|
G | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2224-136C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17700514 | ||||||
chr2:17700721
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2224-343A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17700721 | ||||||
chr2:17700819
|
G | A | 64 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(61): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.2224-441C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17700819 | ||||||
chr2:17701027
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2224-649C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701027 | ||||||
chr2:17701033
|
AAAT | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2224-658_2224-656d others(5): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701033 | ||||||
chr2:17701033
|
AAATAAT | A | 50 | a0001c0001t0002g0206a0002c0003t0001g0007a0002c0003t0001g0008others(47): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.2224-661_2224-656d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701033 | ||||||
chr2:17701033
|
AAATAATA others(2): Show |
A | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(88): Show | 96 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.2224-664_2224-656d others(11): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701033 | ||||||
chr2:17701095
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2224-717C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701095 | ||||||
chr2:17701219
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2223+610A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701219 | ||||||
chr2:17701382
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(172): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2223+447G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701382 | ||||||
chr2:17701388
|
T | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(172): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2223+441A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701388 | ||||||
chr2:17701409
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2223+420A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701409 | ||||||
chr2:17701428
|
CAA | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2223+399_2223+400d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701428 | ||||||
chr2:17701461
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2223+368G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701461 | ||||||
chr2:17701726
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2223+103G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 20/27 | chr2 | 17701726 | ||||||
chr2:17701939
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2143-30G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17701939 | ||||||
chr2:17701951
|
T | A | 49 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(46): Show | 52 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2143-42A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17701951 | ||||||
chr2:17702184
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2143-275A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702184 | ||||||
chr2:17702262
|
G | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2143-353C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702262 | ||||||
chr2:17702327
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2143-418A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702327 | ||||||
chr2:17702366
|
GTATA | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2143-461_2143-458d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702366 | ||||||
chr2:17702609
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2142+548C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702609 | ||||||
chr2:17702730
|
T | A | 1 | a0001c0001t0003g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2142+427A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702730 | ||||||
chr2:17702778
|
T | C | 1 | a0001c0001t0003g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2142+379A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702778 | ||||||
chr2:17702858
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2142+299G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702858 | ||||||
chr2:17702907
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2142+250G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702907 | ||||||
chr2:17702991
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2142+166G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17702991 | ||||||
chr2:17703103
|
C | T | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0225others(1): Show | 4 | HG01891.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+54G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17703103 | ||||||
chr2:17703104
|
G | A | 2 | a0001c0001t0004g0033a0001c0001t0004g0036 | 2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2142+53C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17703104 | ||||||
chr2:17703107
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2142+50C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 19/27 | chr2 | 17703107 | ||||||
chr2:17703315
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.2007-23C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703315 | ||||||
chr2:17703525
|
T | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2007-233A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703525 | ||||||
chr2:17703545
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2007-253C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703545 | ||||||
chr2:17703558
|
TG | T | 27 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(24): Show | 29 | HG00621.hp1 HG00639.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.2007-267delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703558 | ||||||
chr2:17703713
|
C | A | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2007-421G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703713 | ||||||
chr2:17703802
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2007-510A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703802 | ||||||
chr2:17703824
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2007-532A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703824 | ||||||
chr2:17703830
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2007-538C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17703830 | ||||||
chr2:17704360
|
G | A | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2007-1068C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704360 | ||||||
chr2:17704410
|
G | C | 1 | a0001c0001t0003g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2007-1118C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704410 | ||||||
chr2:17704430
|
A | G | 1 | a0001c0001t0013g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2007-1138T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704430 | ||||||
chr2:17704444
|
A | G | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2007-1152T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704444 | ||||||
chr2:17704471
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2007-1179G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704471 | ||||||
chr2:17704587
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2007-1295C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704587 | ||||||
chr2:17704694
|
G | C | 2 | a0003c0002t0001g0162a0003c0002t0001g0163 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2007-1402C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704694 | ||||||
chr2:17704819
|
G | A | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2007-1527C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704819 | ||||||
chr2:17704957
|
TA | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2007-1666delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17704957 | ||||||
chr2:17705115
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2007-1823C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705115 | ||||||
chr2:17705219
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2007-1927G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705219 | ||||||
chr2:17705348
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2006+1871C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705348 | ||||||
chr2:17705349
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2006+1870C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705349 | ||||||
chr2:17705386
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2006+1833A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705386 | ||||||
chr2:17705473
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2006+1746G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705473 | ||||||
chr2:17705605
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2006+1614C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705605 | ||||||
chr2:17705634
|
C | T | 64 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(61): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.2006+1585G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705634 | ||||||
chr2:17705649
|
A | T | 1 | a0001c0001t0002g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2006+1570T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705649 | ||||||
chr2:17705782
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2006+1437G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705782 | ||||||
chr2:17705819
|
A | C | 1 | a0002c0003t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2006+1400T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17705819 | ||||||
chr2:17706196
|
A | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2006+1023T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706196 | ||||||
chr2:17706281
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2006+938C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706281 | ||||||
chr2:17706510
|
TTC | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2006+707_2006+708d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706510 | ||||||
chr2:17706512
|
CT | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2006+706delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706512 | ||||||
chr2:17706513
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.2006+706A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706513 | ||||||
chr2:17706628
|
G | A | 6 | a0002c0003t0001g0008a0002c0003t0001g0152a0002c0003t0001g0164others(3): Show | 7 | HG00280.hp2 HG01168.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2006+591C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706628 | ||||||
chr2:17706642
|
A | T | 1 | a0002c0003t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2006+577T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706642 | ||||||
chr2:17706783
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.2006+436C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706783 | ||||||
chr2:17706848
|
G | C | 1 | a0001c0001t0002g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2006+371C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706848 | ||||||
chr2:17706886
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2006+333A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17706886 | ||||||
chr2:17707100
|
G | A | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2006+119C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17707100 | ||||||
chr2:17707166
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2006+53T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17707166 | ||||||
chr2:17707190
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2006+29C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 18/27 | chr2 | 17707190 | ||||||
chr2:17707571
|
TAA | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1846-194_1846-193d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707571 | ||||||
chr2:17707606
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1846-227G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707606 | ||||||
chr2:17707811
|
G | C | 1 | a0001c0001t0004g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1846-432C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707811 | ||||||
chr2:17707997
|
T | C | 1 | a0001c0001t0003g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1846-618A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707997 | ||||||
chr2:17707997
|
TACAC | T | 4 | a0001c0001t0004g0025a0001c0006t0010g0010a0002c0003t0001g0152others(1): Show | 4 | HG01069.hp1 HG01517.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-622_1846-619d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707997 | ||||||
chr2:17707997
|
TACACAC | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(136): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1846-624_1846-619d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17707997 | ||||||
chr2:17708001
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1846-622G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708001 | ||||||
chr2:17708003
|
C | T | 3 | a0001c0001t0004g0025a0002c0003t0001g0152a0002c0003t0001g0169 | 3 | HG01517.hp2 HG03239.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1846-624G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708003 | ||||||
chr2:17708005
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1846-626G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708005 | ||||||
chr2:17708007
|
C | T | 22 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(19): Show | 24 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1846-628G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708007 | ||||||
chr2:17708108
|
G | A | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG01496.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1845+531C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708108 | ||||||
chr2:17708192
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1845+447G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708192 | ||||||
chr2:17708305
|
A | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1845+334T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708305 | ||||||
chr2:17708311
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1845+328C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708311 | ||||||
chr2:17708434
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1845+205C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708434 | ||||||
chr2:17708438
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1845+201T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708438 | ||||||
chr2:17708524
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1845+115A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708524 | ||||||
chr2:17708589
|
T | C | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1845+50A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 17/27 | chr2 | 17708589 | ||||||
chr2:17708778
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1731-25A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708778 | ||||||
chr2:17708824
|
G | GTA | 53 | a0001c0001t0001g0147a0001c0001t0002g0174a0001c0001t0002g0175others(50): Show | 55 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1731-73_1731-72dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708824 | ||||||
chr2:17708824
|
G | GTATA | 74 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0002g0205others(71): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1731-75_1731-72dup others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708824 | ||||||
chr2:17708824
|
G | GTATATA | 9 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0139others(6): Show | 10 | HG01109.hp2 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1731-77_1731-72dup others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708824 | ||||||
chr2:17708824
|
G | GTGTA | 8 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 10 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1731-72_1731-71ins others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708824 | ||||||
chr2:17708837
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1731-84T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708837 | ||||||
chr2:17708857
|
T | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0104a0001c0001t0002g0111others(3): Show | 7 | HG00408.hp2 HG00438.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1731-104A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17708857 | ||||||
chr2:17709038
|
T | C | 1 | a0001c0001t0003g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1731-285A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709038 | ||||||
chr2:17709103
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1731-350G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709103 | ||||||
chr2:17709230
|
TAC | T | 19 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(16): Show | 19 | HG00639.hp2 HG01074.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1731-479_1731-478d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709230 | ||||||
chr2:17709319
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1731-566A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709319 | ||||||
chr2:17709375
|
T | A | 1 | a0001c0001t0003g0094 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1731-622A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709375 | ||||||
chr2:17709498
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1731-745T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709498 | ||||||
chr2:17709603
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1731-850A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709603 | ||||||
chr2:17709747
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1731-994C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709747 | ||||||
chr2:17709776
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1731-1023T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709776 | ||||||
chr2:17709855
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1731-1102A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709855 | ||||||
chr2:17709899
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1731-1146A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709899 | ||||||
chr2:17709920
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1731-1167A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17709920 | ||||||
chr2:17710216
|
A | G | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1731-1463T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17710216 | ||||||
chr2:17710712
|
T | C | 1 | a0001c0001t0006g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1731-1959A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17710712 | ||||||
chr2:17711047
|
G | C | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-2294C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711047 | ||||||
chr2:17711195
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0003g0103 | 2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1731-2442C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711195 | ||||||
chr2:17711289
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1731-2536T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711289 | ||||||
chr2:17711434
|
A | C | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731-2681T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711434 | ||||||
chr2:17711475
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1731-2722C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711475 | ||||||
chr2:17711816
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1730+3045T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711816 | ||||||
chr2:17711821
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1730+3040T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711821 | ||||||
chr2:17711980
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1730+2881T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17711980 | ||||||
chr2:17712115
|
A | G | 1 | a0003c0002t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1730+2746T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712115 | ||||||
chr2:17712163
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(240): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1730+2698G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712163 | ||||||
chr2:17712210
|
G | A | 7 | a0003c0002t0001g0157a0003c0002t0001g0158a0003c0002t0001g0162others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1730+2651C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712210 | ||||||
chr2:17712277
|
C | T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1730+2584G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712277 | ||||||
chr2:17712413
|
T | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1730+2448A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712413 | ||||||
chr2:17712607
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1730+2254A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712607 | ||||||
chr2:17712638
|
G | T | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1730+2223C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17712638 | ||||||
chr2:17713000
|
C | G | 2 | a0001c0001t0005g0238a0001c0001t0005g0241 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1730+1861G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713000 | ||||||
chr2:17713081
|
C | T | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1730+1780G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713081 | ||||||
chr2:17713083
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1730+1778A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713083 | ||||||
chr2:17713088
|
C | T | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1730+1773G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713088 | ||||||
chr2:17713194
|
C | T | 68 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(65): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1730+1667G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713194 | ||||||
chr2:17713475
|
A | C | 1 | a0001c0001t0005g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1730+1386T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713475 | ||||||
chr2:17713737
|
T | C | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1730+1124A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713737 | ||||||
chr2:17713875
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1730+986C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713875 | ||||||
chr2:17713950
|
A | G | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1730+911T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17713950 | ||||||
chr2:17714029
|
G | A | 1 | a0001c0001t0017g0244 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1730+832C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714029 | ||||||
chr2:17714083
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0004g0039 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1730+768_1730+777d others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714083 | ||||||
chr2:17714092
|
GT | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0142others(81): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1730+768delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714092 | ||||||
chr2:17714092
|
GTT | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(57): Show | 62 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.1730+767_1730+768d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714092 | ||||||
chr2:17714198
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1730+663G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714198 | ||||||
chr2:17714233
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1730+628G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714233 | ||||||
chr2:17714237
|
A | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1730+624T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714237 | ||||||
chr2:17714255
|
C | T | 1 | a0003c0002t0001g0157 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1730+606G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714255 | ||||||
chr2:17714378
|
G | A | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1730+483C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714378 | ||||||
chr2:17714626
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1730+235A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714626 | ||||||
chr2:17714670
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1730+191G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714670 | ||||||
chr2:17714708
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(172): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1730+153G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 16/27 | chr2 | 17714708 | ||||||
chr2:17715123
|
ATCC | A | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1526-61_1526-59del others(3): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715123 | ||||||
chr2:17715147
|
T | C | 2 | a0003c0002t0001g0194a0003c0002t0001g0199 | 2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1526-82A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715147 | ||||||
chr2:17715186
|
T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(22): Show | 28 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1526-121A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715186 | ||||||
chr2:17715267
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1526-202C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715267 | ||||||
chr2:17715443
|
C | T | 7 | a0001c0001t0003g0073a0002c0004t0002g0179a0002c0004t0002g0183others(4): Show | 7 | HG01099.hp2 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-378G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715443 | ||||||
chr2:17715638
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1525+448A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715638 | ||||||
chr2:17715645
|
G | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525+441C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715645 | ||||||
chr2:17715815
|
T | C | 3 | a0001c0001t0003g0086a0001c0001t0003g0091a0001c0001t0003g0105 | 3 | HG01358.hp2 HG02273.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1525+271A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715815 | ||||||
chr2:17715880
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1525+206T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715880 | ||||||
chr2:17715994
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1525+92T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17715994 | ||||||
chr2:17716012
|
CTTCA | C | 10 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0051others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+70_1525+73del others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 15/27 | chr2 | 17716012 | ||||||
chr2:17716491
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1347-227G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 14/27 | chr2 | 17716491 | ||||||
chr2:17716552
|
G | C | 48 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(45): Show | 48 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1346+189C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 14/27 | chr2 | 17716552 | ||||||
chr2:17716631
|
A | G | 6 | a0002c0004t0002g0179a0002c0004t0002g0183a0002c0004t0002g0184others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+110T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 14/27 | chr2 | 17716631 | ||||||
chr2:17717059
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1181+29G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 13/27 | chr2 | 17717059 | ||||||
chr2:17717082
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.1181+6G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 13/27 | chr2 | 17717082 | ||||||
chr2:17717083
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.1181+5G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 13/27 | chr2 | 17717083 | ||||||
chr2:17717397
|
T | C | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1093-221A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717397 | ||||||
chr2:17717447
|
G | A | 58 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(55): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1093-271C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717447 | ||||||
chr2:17717468
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1093-292A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717468 | ||||||
chr2:17717686
|
A | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1092+391T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717686 | ||||||
chr2:17717721
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1092+356G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717721 | ||||||
chr2:17717725
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1092+352A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717725 | ||||||
chr2:17717835
|
T | C | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0016g0138 | 3 | NA18953.hp1 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1092+242A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717835 | ||||||
chr2:17717947
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1092+130A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17717947 | ||||||
chr2:17718024
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1092+53G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 12/27 | chr2 | 17718024 | ||||||
chr2:17718291
|
C | G | 14 | a0003c0002t0001g0009a0003c0002t0001g0189a0003c0002t0001g0190others(11): Show | 15 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.946-68G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718291 | ||||||
chr2:17718317
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.946-94A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718317 | ||||||
chr2:17718481
|
G | T | 1 | a0003c0002t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.946-258C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718481 | ||||||
chr2:17718485
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.946-262A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718485 | ||||||
chr2:17718765
|
T | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.946-542A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718765 | ||||||
chr2:17718792
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.946-569C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718792 | ||||||
chr2:17718827
|
T | C | 1 | a0002c0003t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.946-604A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17718827 | ||||||
chr2:17719064
|
C | A | 1 | a0002c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.946-841G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719064 | ||||||
chr2:17719092
|
G | C | 1 | a0001c0001t0006g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.946-869C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719092 | ||||||
chr2:17719225
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.946-1002G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719225 | ||||||
chr2:17719285
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.946-1062G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719285 | ||||||
chr2:17719611
|
A | C | 1 | a0003c0002t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.945+1329T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719611 | ||||||
chr2:17719714
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.945+1226C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719714 | ||||||
chr2:17719811
|
T | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.945+1129A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719811 | ||||||
chr2:17719830
|
T | C | 1 | a0003c0002t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.945+1110A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17719830 | ||||||
chr2:17720094
|
C | T | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+846G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720094 | ||||||
chr2:17720105
|
T | C | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+835A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720105 | ||||||
chr2:17720218
|
G | A | 48 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0045others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.945+722C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720218 | ||||||
chr2:17720268
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.945+672A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720268 | ||||||
chr2:17720642
|
G | A | 5 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+298C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720642 | ||||||
chr2:17720700
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.945+240A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720700 | ||||||
chr2:17720745
|
A | C | 25 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0011others(22): Show | 27 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.945+195T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720745 | ||||||
chr2:17720815
|
C | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(4): Show | 7 | HG01261.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+125G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720815 | ||||||
chr2:17720903
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.945+37A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 11/27 | chr2 | 17720903 | ||||||
chr2:17721089
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.847-51T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 10/27 | chr2 | 17721089 | ||||||
chr2:17721103
|
T | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+39A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 10/27 | chr2 | 17721103 | ||||||
chr2:17721114
|
C | G | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.846+28G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 10/27 | chr2 | 17721114 | ||||||
chr2:17721464
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.727-203T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721464 | ||||||
chr2:17721699
|
C | CT | 47 | a0001c0001t0001g0140a0001c0001t0001g0171a0001c0001t0002g0219others(44): Show | 50 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.727-439dupA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721699 | ||||||
chr2:17721699
|
CT | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(3): Show | 8 | HG02572.hp2 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-439delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721699 | ||||||
chr2:17721779
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.727-518A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721779 | ||||||
chr2:17721852
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.727-591G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721852 | ||||||
chr2:17721919
|
C | T | 1 | a0001c0001t0004g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.727-658G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17721919 | ||||||
chr2:17722117
|
A | C | 1 | a0002c0003t0001g0152 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.727-856T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722117 | ||||||
chr2:17722355
|
A | G | 51 | a0001c0001t0001g0171a0002c0003t0001g0007a0002c0003t0001g0008others(48): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.727-1094T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722355 | ||||||
chr2:17722368
|
A | G | 1 | a0001c0001t0003g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.727-1107T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722368 | ||||||
chr2:17722610
|
T | C | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.727-1349A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722610 | ||||||
chr2:17722764
|
T | C | 4 | a0001c0001t0003g0041a0001c0001t0003g0068a0001c0001t0003g0099others(1): Show | 4 | HG00423.hp1 NA18971.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1503A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722764 | ||||||
chr2:17722999
|
TA | T | 49 | a0001c0001t0001g0148a0001c0001t0002g0174a0001c0001t0002g0175others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.727-1739delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17722999 | ||||||
chr2:17723023
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.727-1762C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723023 | ||||||
chr2:17723029
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.727-1768T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723029 | ||||||
chr2:17723070
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.727-1809T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723070 | ||||||
chr2:17723107
|
GTCAT | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.727-1850_727-1847d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723107 | ||||||
chr2:17723117
|
C | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-1856G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723117 | ||||||
chr2:17723427
|
C | T | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.726+1830G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723427 | ||||||
chr2:17723576
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+1681A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723576 | ||||||
chr2:17723578
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+1679T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723578 | ||||||
chr2:17723581
|
C | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+1676G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723581 | ||||||
chr2:17723606
|
T | C | 1 | a0001c0001t0005g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.726+1651A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723606 | ||||||
chr2:17723833
|
T | C | 14 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 15 | HG00621.hp1 NA18945.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.726+1424A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17723833 | ||||||
chr2:17724145
|
TAC | T | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1110_726+1111d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724145 | ||||||
chr2:17724183
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.726+1074T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724183 | ||||||
chr2:17724209
|
T | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+1048A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724209 | ||||||
chr2:17724522
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.726+735G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724522 | ||||||
chr2:17724581
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.726+676A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724581 | ||||||
chr2:17724611
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+646C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724611 | ||||||
chr2:17724829
|
C | T | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.726+428G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 9/27 | chr2 | 17724829 | ||||||
chr2:17725372
|
C | CA | 5 | a0001c0001t0002g0176a0001c0001t0002g0219a0001c0001t0003g0076others(2): Show | 5 | HG01496.hp2 HG03098.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-15dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17725372 | ||||||
chr2:17725382
|
C | T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.625-24G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17725382 | ||||||
chr2:17725516
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.625-158A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17725516 | ||||||
chr2:17725852
|
C | A | 5 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0037others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-494G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17725852 | ||||||
chr2:17726087
|
T | TA | 32 | a0001c0001t0001g0016a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 34 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.624+301dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAA | 7 | a0001c0001t0001g0149a0001c0001t0002g0119a0001c0001t0002g0123others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+300_624+301dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAA | 13 | a0001c0001t0003g0053a0001c0001t0004g0003a0001c0001t0004g0022others(10): Show | 14 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.624+299_624+301dup others(3): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAA | 7 | a0001c0001t0001g0147a0001c0001t0004g0023a0001c0001t0004g0025others(4): Show | 7 | HG03098.hp1 HG03579.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+298_624+301dup others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAA | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0005g0234others(7): Show | 10 | HG02056.hp1 HG03130.hp1 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+296_624+301dup others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(2): Show |
14 | a0001c0001t0002g0202a0001c0001t0002g0205a0001c0001t0002g0207others(11): Show | 14 | HG00639.hp2 HG01071.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.624+293_624+301dup others(9): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(3): Show |
7 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0208others(4): Show | 7 | HG01069.hp2 HG01070.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+292_624+301dup others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(4): Show |
11 | a0001c0001t0002g0211a0001c0001t0002g0214a0001c0001t0002g0218others(8): Show | 11 | HG01433.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+291_624+301dup others(11): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(5): Show |
1 | a0002c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.624+290_624+301dup others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.624+288_624+301dup others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0002g0227a0002c0004t0002g0183 | 2 | HG02055.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.624+287_624+301dup others(15): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(9): Show |
3 | a0002c0004t0002g0184a0002c0004t0002g0185a0002c0004t0002g0186 | 3 | HG02970.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.624+286_624+301dup others(16): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(15): Show |
1 | a0002c0004t0002g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.624+280_624+301dup others(22): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(21): Show |
1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.624+301_624+302ins others(28): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
T | TAAAAAAA others(37): Show |
1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+301_624+302ins others(44): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
TA | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0002g0085others(8): Show | 12 | HG01069.hp1 HG01168.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+301delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
TAA | T | 36 | a0001c0001t0007g0006a0002c0003t0001g0008a0002c0003t0001g0151others(33): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+300_624+301del others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
TAAA | T | 5 | a0002c0003t0001g0007a0002c0003t0001g0153a0002c0003t0001g0154others(2): Show | 6 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+299_624+301del others(3): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726087
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0004g0037a0001c0001t0004g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.624+288_624+301del others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726087 | ||||||
chr2:17726115
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.624+274C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726115 | ||||||
chr2:17726246
|
A | G | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.624+143T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726246 | ||||||
chr2:17726247
|
T | A | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.624+142A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726247 | ||||||
chr2:17726248
|
C | T | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.624+141G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726248 | ||||||
chr2:17726251
|
GGAAATT | G | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.624+132_624+137del others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726251 | ||||||
chr2:17726252
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.624+137C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726252 | ||||||
chr2:17726272
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.624+117T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726272 | ||||||
chr2:17726296
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.624+93G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 8/27 | chr2 | 17726296 | ||||||
chr2:17726599
|
C | G | 1 | a0001c0001t0004g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.544-130G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17726599 | ||||||
chr2:17726676
|
A | G | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-207T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17726676 | ||||||
chr2:17726779
|
C | G | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.544-310G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17726779 | ||||||
chr2:17726780
|
T | G | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.544-311A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17726780 | ||||||
chr2:17726863
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(167): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.544-394A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17726863 | ||||||
chr2:17727110
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.544-641G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727110 | ||||||
chr2:17727156
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-687C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727156 | ||||||
chr2:17727169
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.544-700C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727169 | ||||||
chr2:17727460
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-991A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727460 | ||||||
chr2:17727505
|
T | TTA | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-1038_544-1037d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727505 | ||||||
chr2:17727505
|
TTA | T | 109 | a0001c0001t0001g0147a0001c0001t0002g0005a0001c0001t0002g0012others(106): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.544-1038_544-1037d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727505 | ||||||
chr2:17727505
|
TTATA | T | 113 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(110): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.544-1040_544-1037d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727505 | ||||||
chr2:17727505
|
TTATATA | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.544-1042_544-1037d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727505 | ||||||
chr2:17727520
|
T | A | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.544-1051A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727520 | ||||||
chr2:17727526
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0147others(2): Show | 7 | HG01069.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-1057A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727526 | ||||||
chr2:17727614
|
A | G | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.544-1145T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727614 | ||||||
chr2:17727709
|
A | G | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.544-1240T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727709 | ||||||
chr2:17727721
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.544-1252T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727721 | ||||||
chr2:17727832
|
G | T | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-1363C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727832 | ||||||
chr2:17727910
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.544-1441A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727910 | ||||||
chr2:17727959
|
C | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 34 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-1490G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17727959 | ||||||
chr2:17728003
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.544-1534A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728003 | ||||||
chr2:17728208
|
G | A | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.544-1739C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728208 | ||||||
chr2:17728248
|
C | A | 1 | a0001c0001t0003g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.544-1779G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728248 | ||||||
chr2:17728382
|
C | T | 23 | a0001c0001t0001g0147a0001c0001t0004g0003a0001c0001t0004g0022others(20): Show | 25 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.544-1913G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728382 | ||||||
chr2:17728416
|
A | G | 1 | a0001c0001t0004g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.544-1947T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728416 | ||||||
chr2:17728518
|
A | C | 1 | a0001c0001t0003g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.544-2049T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728518 | ||||||
chr2:17728558
|
AG | A | 9 | a0001c0001t0003g0059a0001c0001t0003g0072a0001c0001t0003g0074others(6): Show | 9 | NA18953.hp1 NA18968.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-2090delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728558 | ||||||
chr2:17728591
|
G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 34 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-2122C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728591 | ||||||
chr2:17728639
|
C | G | 2 | a0001c0001t0002g0082a0001c0001t0002g0085 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.544-2170G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728639 | ||||||
chr2:17728753
|
A | AT | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.544-2285dupA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728753 | ||||||
chr2:17728965
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+2113C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728965 | ||||||
chr2:17728991
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.543+2087G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17728991 | ||||||
chr2:17729084
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(142): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.543+1994G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729084 | ||||||
chr2:17729318
|
T | A | 1 | a0001c0001t0002g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.543+1760A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729318 | ||||||
chr2:17729343
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.543+1735G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729343 | ||||||
chr2:17729464
|
TAATA | T | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+1610_543+1613d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729464 | ||||||
chr2:17729659
|
G | T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.543+1419C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729659 | ||||||
chr2:17729676
|
A | T | 1 | a0001c0001t0003g0053 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.543+1402T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729676 | ||||||
chr2:17729895
|
T | C | 50 | a0002c0003t0001g0007a0002c0003t0001g0008a0002c0003t0001g0151others(47): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.543+1183A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17729895 | ||||||
chr2:17730244
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+834A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730244 | ||||||
chr2:17730246
|
T | C | 1 | a0001c0001t0003g0057 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.543+832A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730246 | ||||||
chr2:17730338
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.543+740A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730338 | ||||||
chr2:17730371
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0014g0050 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.543+707G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730371 | ||||||
chr2:17730398
|
G | GA | 41 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0142others(38): Show | 42 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.543+679dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730398 | ||||||
chr2:17730398
|
G | GAA | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+678_543+679dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730398 | ||||||
chr2:17730398
|
GA | G | 26 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(23): Show | 27 | HG00621.hp1 HG00639.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.543+679delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730398 | ||||||
chr2:17730580
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(167): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.543+498C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730580 | ||||||
chr2:17730603
|
CT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(69): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.543+474delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730603 | ||||||
chr2:17730747
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.543+331G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730747 | ||||||
chr2:17730751
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.543+327G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730751 | ||||||
chr2:17730769
|
A | AT | 6 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(3): Show | 7 | HG02572.hp2 HG02896.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+308dupA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730769 | ||||||
chr2:17730769
|
A | ATT | 22 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0004g0003others(19): Show | 24 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+307_543+308dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730769 | ||||||
chr2:17730944
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.543+134A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17730944 | ||||||
chr2:17731033
|
T | C | 1 | a0004c0008t0012g0195 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.543+45A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17731033 | ||||||
chr2:17731068
|
C | T | 3 | a0001c0001t0003g0086a0001c0001t0003g0091a0001c0001t0003g0105 | 3 | HG01358.hp2 HG02273.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.543+10G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 7/27 | chr2 | 17731068 | ||||||
chr2:17731364
|
T | A | 1 | a0001c0001t0002g0159 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.482-225A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731364 | ||||||
chr2:17731544
|
T | C | 4 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(1): Show | 4 | HG00099.hp1 HG01256.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+197A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731544 | ||||||
chr2:17731597
|
C | CGT | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+142_481+143dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731597 | ||||||
chr2:17731597
|
C | CGTGT | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.481+140_481+143dup others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731597 | ||||||
chr2:17731597
|
CGT | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0066a0003c0002t0001g0196 | 4 | HG02717.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+142_481+143del others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731597 | ||||||
chr2:17731614
|
G | A | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.481+127C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731614 | ||||||
chr2:17731669
|
C | A | 1 | a0003c0002t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.481+72G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 6/27 | chr2 | 17731669 | ||||||
chr2:17731999
|
A | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(240): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.345-122T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17731999 | ||||||
chr2:17732048
|
G | A | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0225others(1): Show | 4 | HG01891.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-171C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732048 | ||||||
chr2:17732090
|
G | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.345-213C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732090 | ||||||
chr2:17732135
|
A | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.345-258T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732135 | ||||||
chr2:17732149
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.345-272T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732149 | ||||||
chr2:17732273
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-396A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732273 | ||||||
chr2:17732358
|
A | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-481T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732358 | ||||||
chr2:17732448
|
C | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.345-571G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732448 | ||||||
chr2:17732496
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.345-619G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732496 | ||||||
chr2:17732677
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.345-800G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732677 | ||||||
chr2:17732698
|
CA | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(141): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.345-822delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732698 | ||||||
chr2:17732789
|
G | T | 112 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(109): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.345-912C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732789 | ||||||
chr2:17732790
|
C | G | 1 | a0001c0001t0003g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.345-913G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732790 | ||||||
chr2:17732994
|
A | T | 1 | a0001c0001t0002g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345-1117T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17732994 | ||||||
chr2:17733051
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.345-1174C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733051 | ||||||
chr2:17733180
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.345-1303C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733180 | ||||||
chr2:17733356
|
A | G | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-1479T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733356 | ||||||
chr2:17733359
|
G | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(18): Show | 22 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.345-1482C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733359 | ||||||
chr2:17733540
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-1663C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733540 | ||||||
chr2:17733657
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-1780A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733657 | ||||||
chr2:17733972
|
G | C | 30 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(27): Show | 30 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-2095C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17733972 | ||||||
chr2:17734009
|
A | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.345-2132T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734009 | ||||||
chr2:17734061
|
T | C | 1 | a0001c0001t0003g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.345-2184A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734061 | ||||||
chr2:17734095
|
C | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.345-2218G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734095 | ||||||
chr2:17734208
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.345-2331T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734208 | ||||||
chr2:17734253
|
C | T | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-2376G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734253 | ||||||
chr2:17734460
|
TATGAGGG others(96): Show |
T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.345-2686_345-2584d others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734460 | ||||||
chr2:17734492
|
G | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0091a0001c0001t0003g0105 | 3 | HG01358.hp2 HG02273.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.345-2615C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734492 | ||||||
chr2:17734564
|
A | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.345-2687T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734564 | ||||||
chr2:17734565
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.345-2688A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734565 | ||||||
chr2:17734649
|
C | G | 20 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(17): Show | 21 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.345-2772G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734649 | ||||||
chr2:17734731
|
CTTTTCTT others(1): Show |
C | 52 | a0001c0001t0001g0171a0001c0001t0002g0159a0002c0003t0001g0007others(49): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.345-2862_345-2855d others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734731 | ||||||
chr2:17734820
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.345-2943G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734820 | ||||||
chr2:17734928
|
C | T | 3 | a0001c0001t0002g0081a0001c0001t0002g0088a0001c0001t0002g0092 | 3 | HG02074.hp2 HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.345-3051G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17734928 | ||||||
chr2:17735036
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG01081.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.345-3159A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735036 | ||||||
chr2:17735115
|
C | G | 52 | a0001c0001t0001g0171a0001c0001t0002g0159a0002c0003t0001g0007others(49): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.344+3106G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735115 | ||||||
chr2:17735115
|
CAAACA | C | 22 | a0001c0001t0001g0147a0001c0001t0004g0003a0001c0001t0004g0022others(19): Show | 24 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.344+3101_344+3105d others(7): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735115 | ||||||
chr2:17735202
|
G | A | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.344+3019C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735202 | ||||||
chr2:17735227
|
C | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+2994G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735227 | ||||||
chr2:17735257
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.344+2964T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735257 | ||||||
chr2:17735283
|
G | T | 20 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(17): Show | 21 | HG00621.hp1 HG00639.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.344+2938C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735283 | ||||||
chr2:17735366
|
C | G | 1 | a0001c0001t0002g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.344+2855G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735366 | ||||||
chr2:17735553
|
T | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.344+2668A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17735553 | ||||||
chr2:17736008
|
G | T | 5 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+2213C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736008 | ||||||
chr2:17736520
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.344+1701C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736520 | ||||||
chr2:17736531
|
C | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 33 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(30): Show |
intron_variant | MODIFIER | c.344+1690G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736531 | ||||||
chr2:17736606
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.344+1615C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736606 | ||||||
chr2:17736685
|
C | G | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+1536G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736685 | ||||||
chr2:17736707
|
T | TA | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.344+1513dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736707 | ||||||
chr2:17736725
|
T | A | 1 | a0001c0001t0003g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.344+1496A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736725 | ||||||
chr2:17736726
|
T | A | 1 | a0001c0001t0003g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.344+1495A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736726 | ||||||
chr2:17736788
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.344+1433G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736788 | ||||||
chr2:17736871
|
CA | C | 66 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(63): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.344+1349delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736871 | ||||||
chr2:17736899
|
T | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(240): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.344+1322A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736899 | ||||||
chr2:17736965
|
T | C | 2 | a0003c0002t0001g0200a0003c0002t0001g0201 | 2 | HG00140.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.344+1256A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17736965 | ||||||
chr2:17737037
|
C | T | 1 | a0001c0001t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.344+1184G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737037 | ||||||
chr2:17737186
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.344+1035T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737186 | ||||||
chr2:17737218
|
C | T | 1 | a0003c0002t0001g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.344+1003G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737218 | ||||||
chr2:17737445
|
T | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+776A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737445 | ||||||
chr2:17737733
|
GT | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+487delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737733 | ||||||
chr2:17737920
|
A | T | 2 | a0001c0001t0003g0109a0001c0001t0014g0050 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.344+301T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737920 | ||||||
chr2:17737983
|
C | T | 4 | a0002c0004t0002g0183a0002c0004t0002g0184a0002c0004t0002g0185others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+238G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737983 | ||||||
chr2:17737988
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344+233A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17737988 | ||||||
chr2:17738000
|
G | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 33 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(30): Show |
intron_variant | MODIFIER | c.344+221C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17738000 | ||||||
chr2:17738099
|
C | T | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+122G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 5/27 | chr2 | 17738099 | ||||||
chr2:17738351
|
TCA | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-27_239-26delTG | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17738351 | ||||||
chr2:17738356
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.239-30A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17738356 | ||||||
chr2:17738786
|
G | A | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.239-460C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17738786 | ||||||
chr2:17738966
|
T | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.239-640A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17738966 | ||||||
chr2:17738998
|
T | TATTG | 47 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.239-676_239-673dup others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17738998 | ||||||
chr2:17739019
|
C | G | 4 | a0002c0004t0002g0183a0002c0004t0002g0184a0002c0004t0002g0185others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-693G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739019 | ||||||
chr2:17739047
|
G | A | 11 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(8): Show | 11 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-721C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739047 | ||||||
chr2:17739189
|
C | G | 4 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0054others(1): Show | 4 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-863G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739189 | ||||||
chr2:17739196
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.239-870G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739196 | ||||||
chr2:17739258
|
C | T | 4 | a0002c0004t0002g0183a0002c0004t0002g0184a0002c0004t0002g0185others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-932G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739258 | ||||||
chr2:17739278
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.239-952T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739278 | ||||||
chr2:17739300
|
G | C | 47 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.239-974C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739300 | ||||||
chr2:17739433
|
C | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0034others(1): Show | 4 | NA18957.hp1 NA18979.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-1107G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739433 | ||||||
chr2:17739558
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.239-1232A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739558 | ||||||
chr2:17739769
|
C | A | 68 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(65): Show | 71 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.239-1443G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739769 | ||||||
chr2:17739818
|
TTAAACAC others(51): Show |
T | 3 | a0001c0001t0004g0028a0001c0001t0004g0033a0001c0001t0004g0039 | 3 | NA18979.hp1 NA19006.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.239-1550_239-1493d others(60): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739818 | ||||||
chr2:17739821
|
A | AAC | 3 | a0001c0001t0001g0001a0001c0001t0006g0042a0003c0002t0001g0162 | 5 | HG01255.hp2 HG01258.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1497_239-1496d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739821 | ||||||
chr2:17739821
|
AAC | A | 3 | a0001c0001t0001g0147a0001c0001t0002g0126a0001c0001t0007g0006 | 4 | HG02572.hp2 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-1497_239-1496d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739821 | ||||||
chr2:17739821
|
AACACACA others(53): Show |
A | 6 | a0001c0001t0004g0003a0001c0001t0004g0024a0001c0001t0004g0030others(3): Show | 7 | NA18945.hp1 NA18957.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-1555_239-1496d others(62): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739821 | ||||||
chr2:17739823
|
CACACACA others(49): Show |
C | 6 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0025others(3): Show | 6 | HG00621.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-1553_239-1498d others(58): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739823 | ||||||
chr2:17739825
|
CACACACA others(47): Show |
C | 3 | a0001c0001t0004g0027a0001c0001t0004g0031a0001c0001t0004g0040 | 3 | HG03098.hp1 NA19001.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.239-1553_239-1500d others(56): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739825 | ||||||
chr2:17739827
|
CACACACA others(45): Show |
C | 2 | a0001c0001t0004g0029a0001c0001t0004g0032 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.239-1553_239-1502d others(54): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739827 | ||||||
chr2:17739829
|
C | G | 4 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0054others(1): Show | 4 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-1503G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739829 | ||||||
chr2:17739837
|
C | CACACACA others(3): Show |
2 | a0001c0001t0001g0171a0001c0001t0002g0214 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-1512_239-1511i others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739837 | ||||||
chr2:17739839
|
C | CACACACA others(3): Show |
3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.239-1514_239-1513i others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739839 | ||||||
chr2:17739839
|
C | CACACACA others(1): Show |
10 | a0001c0001t0005g0234a0001c0001t0005g0236a0001c0001t0005g0237others(7): Show | 10 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-1514_239-1513i others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739839 | ||||||
chr2:17739841
|
C | CACACAG | 18 | a0001c0001t0002g0159a0002c0003t0001g0007a0002c0003t0001g0008others(15): Show | 20 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-1516_239-1515i others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739841 | ||||||
chr2:17739843
|
CAG | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0005t0001g0021 | 3 | HG02280.hp1 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.239-1519_239-1518d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739843 | ||||||
chr2:17739845
|
G | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(35): Show | 42 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.239-1519C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739845
|
G | GAC | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0006t0010g0010 | 3 | HG01069.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.239-1521_239-1520d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739845
|
G | GACAC | 40 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0002g0206others(37): Show | 41 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.239-1523_239-1520d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739845
|
G | GACACAC | 3 | a0001c0001t0001g0146a0001c0001t0002g0187a0002c0004t0002g0185 | 3 | HG00140.hp1 HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-1525_239-1520d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739845
|
G | GACACACA others(1): Show |
28 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(25): Show | 28 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.239-1527_239-1520d others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739845
|
G | GACACACA others(3): Show |
1 | a0001c0001t0002g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-1529_239-1520d others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739845 | ||||||
chr2:17739879
|
A | AAC | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 24 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.239-1555_239-1554d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACAC | 21 | a0001c0001t0001g0016a0001c0001t0001g0142a0001c0001t0001g0143others(18): Show | 22 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.239-1557_239-1554d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACAC | 16 | a0001c0001t0002g0088a0001c0001t0002g0126a0001c0001t0002g0187others(13): Show | 16 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-1559_239-1554d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(1): Show |
11 | a0001c0001t0002g0085a0001c0001t0002g0117a0001c0001t0003g0051others(8): Show | 11 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-1561_239-1554d others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(3): Show |
12 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0111others(9): Show | 12 | HG00438.hp2 HG00642.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-1563_239-1554d others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(5): Show |
15 | a0001c0001t0002g0116a0001c0001t0002g0125a0001c0001t0003g0045others(12): Show | 15 | HG00423.hp1 HG00558.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.239-1565_239-1554d others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(7): Show |
5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG01243.hp2 NA18979.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1567_239-1554d others(16): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(9): Show |
2 | a0001c0001t0003g0041a0001c0001t0003g0072 | 2 | NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.239-1569_239-1554d others(18): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(11): Show |
1 | a0001c0001t0005g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.239-1571_239-1554d others(20): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
A | AACACACA others(19): Show |
1 | a0001c0001t0003g0071 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.239-1579_239-1554d others(28): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AAC | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG02698.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-1555_239-1554d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACAC | A | 9 | a0001c0001t0002g0205a0001c0001t0002g0210a0001c0001t0002g0212others(6): Show | 9 | HG00639.hp2 HG01074.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-1557_239-1554d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACAC | A | 30 | a0001c0001t0001g0066a0001c0001t0001g0148a0001c0001t0001g0149others(27): Show | 30 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.239-1559_239-1554d others(8): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(1): Show |
A | 31 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0209others(28): Show | 34 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.239-1561_239-1554d others(10): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0002g0211a0001c0001t0002g0226a0001c0001t0003g0098others(6): Show | 9 | HG00099.hp1 HG01069.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-1563_239-1554d others(12): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(5): Show |
A | 14 | a0001c0001t0002g0227a0002c0003t0001g0007a0002c0003t0001g0152others(11): Show | 16 | HG00140.hp2 HG01175.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-1565_239-1554d others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(7): Show |
A | 4 | a0001c0001t0003g0063a0001c0001t0005g0236a0003c0002t0001g0191others(1): Show | 4 | HG00735.hp2 HG01192.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-1567_239-1554d others(16): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(11): Show |
A | 1 | a0003c0002t0009g0233 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239-1571_239-1554d others(20): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.239-1575_239-1554d others(24): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17739879
|
AACACACA others(17): Show |
A | 2 | a0002c0003t0001g0144a0002c0003t0001g0145 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.239-1577_239-1554d others(26): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17739879 | ||||||
chr2:17740316
|
G | C | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.238+1296C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740316 | ||||||
chr2:17740349
|
A | T | 1 | a0001c0001t0003g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.238+1263T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740349 | ||||||
chr2:17740353
|
T | C | 1 | a0002c0003t0001g0170 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238+1259A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740353 | ||||||
chr2:17740424
|
C | T | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.238+1188G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740424 | ||||||
chr2:17740498
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.238+1114G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740498 | ||||||
chr2:17740799
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.238+813C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740799 | ||||||
chr2:17740831
|
T | C | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+781A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740831 | ||||||
chr2:17740848
|
TCAAAAAA others(8): Show |
T | 9 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(6): Show | 9 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+749_238+763del others(15): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740848 | ||||||
chr2:17740858
|
AAAAAACA others(7): Show |
A | 2 | a0001c0001t0005g0239a0001c0001t0017g0244 | 2 | NA18959.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.238+740_238+753del others(14): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740858 | ||||||
chr2:17740862
|
AAC | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.238+748_238+749del others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740862 | ||||||
chr2:17740863
|
AC | A | 29 | a0001c0001t0001g0139a0001c0001t0002g0174a0001c0001t0002g0175others(26): Show | 29 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.238+748delG | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740863 | ||||||
chr2:17740864
|
C | A | 76 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(73): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.238+748G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740864 | ||||||
chr2:17740872
|
C | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+740G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17740872 | ||||||
chr2:17741074
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.238+538A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17741074 | ||||||
chr2:17741248
|
T | G | 2 | a0001c0001t0003g0099a0001c0001t0003g0100 | 2 | HG00423.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.238+364A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17741248 | ||||||
chr2:17741572
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.238+40C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17741572 | ||||||
chr2:17741598
|
G | C | 14 | a0001c0001t0004g0003a0001c0001t0004g0022a0001c0001t0004g0023others(11): Show | 15 | HG00621.hp1 NA18945.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+14C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 4/27 | chr2 | 17741598 | ||||||
chr2:17741774
|
T | A | 1 | a0002c0003t0001g0170 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.121-45A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17741774 | ||||||
chr2:17742076
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 78 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.121-347G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742076 | ||||||
chr2:17742084
|
C | T | 1 | a0001c0001t0004g0028 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.121-355G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742084 | ||||||
chr2:17742105
|
A | T | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.121-376T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742105 | ||||||
chr2:17742167
|
T | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-438A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742167 | ||||||
chr2:17742378
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.121-649A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742378 | ||||||
chr2:17742659
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.121-930G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17742659 | ||||||
chr2:17743240
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.121-1511T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743240 | ||||||
chr2:17743246
|
C | T | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.121-1517G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743246 | ||||||
chr2:17743266
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.121-1537G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743266 | ||||||
chr2:17743355
|
C | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121-1626G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743355 | ||||||
chr2:17743405
|
CCTAA | C | 3 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0230 | 3 | HG00639.hp2 HG01074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121-1680_121-1677d others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743405 | ||||||
chr2:17743410
|
C | CTAAG | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.121-1682_121-1681i others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743410 | ||||||
chr2:17743540
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.121-1811G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743540 | ||||||
chr2:17743587
|
C | G | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.121-1858G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743587 | ||||||
chr2:17743617
|
G | A | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-1888C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743617 | ||||||
chr2:17743676
|
CAT | C | 5 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-1949_121-1948d others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743676 | ||||||
chr2:17743699
|
G | C | 1 | a0001c0001t0013g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.121-1970C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743699 | ||||||
chr2:17743717
|
C | T | 2 | a0001c0001t0003g0069a0001c0006t0010g0010 | 2 | HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.121-1988G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17743717 | ||||||
chr2:17744075
|
A | C | 1 | a0001c0001t0005g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+1752T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744075 | ||||||
chr2:17744219
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 78 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.120+1608A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744219 | ||||||
chr2:17744256
|
T | C | 45 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.120+1571A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744256 | ||||||
chr2:17744307
|
G | A | 5 | a0002c0003t0001g0151a0002c0003t0001g0172a0002c0003t0001g0181others(2): Show | 5 | HG02717.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+1520C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744307 | ||||||
chr2:17744444
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.120+1383G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744444 | ||||||
chr2:17744522
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+1305T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744522 | ||||||
chr2:17744715
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+1112A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744715 | ||||||
chr2:17744736
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 78 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.120+1091C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744736 | ||||||
chr2:17744894
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.120+933A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744894 | ||||||
chr2:17744952
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.120+875A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744952 | ||||||
chr2:17744979
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0066 | 3 | HG02717.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.120+848G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17744979 | ||||||
chr2:17745044
|
C | CTTCA | 3 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0103 | 3 | HG01346.hp1 HG02074.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.120+782_120+783ins others(4): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745044 | ||||||
chr2:17745059
|
G | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+768C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745059 | ||||||
chr2:17745060
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+767A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745060 | ||||||
chr2:17745254
|
A | G | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG01496.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.120+573T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745254 | ||||||
chr2:17745257
|
CTG | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 9 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+568_120+569del others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745257 | ||||||
chr2:17745292
|
TG | T | 34 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.120+534delC | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745292 | ||||||
chr2:17745345
|
T | C | 1 | a0001c0001t0005g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+482A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745345 | ||||||
chr2:17745522
|
G | C | 31 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.120+305C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745522 | ||||||
chr2:17745606
|
T | C | 1 | a0003c0002t0001g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.120+221A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745606 | ||||||
chr2:17745658
|
AT | A | 24 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(21): Show | 26 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+168delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 3/27 | chr2 | 17745658 | ||||||
chr2:17745999
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG01081.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-5-48A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17745999 | ||||||
chr2:17746008
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-5-57G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746008 | ||||||
chr2:17746157
|
T | G | 1 | a0001c0001t0003g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5-206A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746157 | ||||||
chr2:17746209
|
A | G | 4 | a0001c0001t0003g0041a0001c0001t0003g0068a0001c0001t0003g0130others(1): Show | 4 | NA18971.hp2 NA18978.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-258T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746209 | ||||||
chr2:17746304
|
T | C | 47 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-5-353A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746304 | ||||||
chr2:17746592
|
T | TA | 22 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 25 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5-642dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746592 | ||||||
chr2:17746599
|
A | AT | 5 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0037others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-649_-5-648insA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746599 | ||||||
chr2:17746605
|
C | CAGGTTGA others(1): Show |
2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-5-662_-5-655dupAT others(6): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746605 | ||||||
chr2:17746615
|
G | C | 1 | a0001c0001t0003g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-5-664C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746615 | ||||||
chr2:17746671
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5-720T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746671 | ||||||
chr2:17746695
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5-744A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746695 | ||||||
chr2:17746703
|
C | T | 1 | a0001c0001t0003g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-5-752G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746703 | ||||||
chr2:17746707
|
A | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5-756T>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746707 | ||||||
chr2:17746821
|
A | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-870T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746821 | ||||||
chr2:17746871
|
T | A | 1 | a0001c0001t0003g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5-920A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746871 | ||||||
chr2:17746940
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-989G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17746940 | ||||||
chr2:17747008
|
G | A | 4 | a0002c0004t0002g0183a0002c0004t0002g0184a0002c0004t0002g0185others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-1057C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747008 | ||||||
chr2:17747035
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-5-1084G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747035 | ||||||
chr2:17747128
|
G | C | 1 | a0001c0001t0002g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5-1177C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747128 | ||||||
chr2:17747139
|
T | G | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-5-1188A>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747139 | ||||||
chr2:17747368
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-1417A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747368 | ||||||
chr2:17747382
|
T | C | 2 | a0001c0001t0004g0037a0001c0001t0004g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5-1431A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747382 | ||||||
chr2:17747482
|
T | A | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-1531A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747482 | ||||||
chr2:17747489
|
CT | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-1539delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747489 | ||||||
chr2:17747503
|
CTTTCT | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0139others(2): Show | 6 | HG02717.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-1557_-5-1553del others(5): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747503 | ||||||
chr2:17747507
|
CT | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(208): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-5-1557delA | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747507 | ||||||
chr2:17747652
|
G | A | 2 | a0003c0002t0001g0198a0003c0002t0011g0197 | 2 | NA18955.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-5-1701C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17747652 | ||||||
chr2:17748238
|
A | G | 2 | a0003c0002t0001g0157a0003c0002t0001g0158 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-5-2287T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748238 | ||||||
chr2:17748439
|
A | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-2488T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748439 | ||||||
chr2:17748469
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-5-2518G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748469 | ||||||
chr2:17748835
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-2884T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748835 | ||||||
chr2:17748851
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-5-2900G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748851 | ||||||
chr2:17748902
|
T | C | 7 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0135others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-2951A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748902 | ||||||
chr2:17748917
|
C | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-2966G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748917 | ||||||
chr2:17748928
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 78 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-5-2977C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17748928 | ||||||
chr2:17749014
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-3063C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749014 | ||||||
chr2:17749081
|
T | A | 1 | a0001c0001t0013g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-3130A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749081 | ||||||
chr2:17749295
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-3344A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749295 | ||||||
chr2:17749463
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-5-3512C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749463 | ||||||
chr2:17749539
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-6+3439A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749539 | ||||||
chr2:17749554
|
GGC | G | 6 | a0002c0003t0001g0007a0002c0003t0001g0153a0002c0003t0001g0154others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+3422_-6+3423del others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749554 | ||||||
chr2:17749558
|
C | T | 1 | a0001c0001t0007g0006 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-6+3420G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749558 | ||||||
chr2:17749607
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 80 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-6+3371T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749607 | ||||||
chr2:17749851
|
C | T | 47 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0174others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-6+3127G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17749851 | ||||||
chr2:17750237
|
G | A | 1 | a0001c0006t0010g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-6+2741C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17750237 | ||||||
chr2:17750654
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0002c0003t0001g0133others(6): Show | 9 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+2324A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17750654 | ||||||
chr2:17750742
|
T | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(4): Show | 7 | HG01261.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+2236A>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17750742 | ||||||
chr2:17750846
|
CA | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-6+2131delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17750846 | ||||||
chr2:17750989
|
G | C | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG01496.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-6+1989C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17750989 | ||||||
chr2:17751005
|
C | CA | 82 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-6+1972dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751005 | ||||||
chr2:17751005
|
C | CAA | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-6+1971_-6+1972dup others(2): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751005 | ||||||
chr2:17751005
|
C | CAAA | 12 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(9): Show | 13 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6+1970_-6+1972dup others(3): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751005 | ||||||
chr2:17751215
|
C | T | 1 | a0001c0001t0003g0046 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-6+1763G>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751215 | ||||||
chr2:17751276
|
C | G | 1 | a0001c0001t0004g0028 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-6+1702G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751276 | ||||||
chr2:17751425
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-6+1553A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751425 | ||||||
chr2:17751448
|
A | C | 1 | a0001c0001t0003g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-6+1530T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751448 | ||||||
chr2:17751449
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-6+1529C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751449 | ||||||
chr2:17751467
|
C | CA | 7 | a0001c0001t0002g0132a0001c0001t0002g0229a0001c0001t0003g0130others(4): Show | 7 | HG00140.hp2 HG01175.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+1510dupT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751467 | ||||||
chr2:17751467
|
CA | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 74 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.-6+1510delT | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751467 | ||||||
chr2:17751566
|
G | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-6+1412C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751566 | ||||||
chr2:17751601
|
C | G | 1 | a0001c0001t0003g0044 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-6+1377G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751601 | ||||||
chr2:17751606
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-6+1372C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751606 | ||||||
chr2:17751721
|
G | C | 1 | a0002c0003t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-6+1257C>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751721 | ||||||
chr2:17751893
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+1085T>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17751893 | ||||||
chr2:17752008
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-6+970A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752008 | ||||||
chr2:17752052
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0007g0006 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-6+926A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752052 | ||||||
chr2:17752170
|
C | G | 1 | a0001c0001t0005g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-6+808G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752170 | ||||||
chr2:17752566
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-6+412T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752566 | ||||||
chr2:17752604
|
A | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG03669.hp2 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-6+374T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752604 | ||||||
chr2:17752727
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+251G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752727 | ||||||
chr2:17752895
|
T | C | 52 | a0001c0001t0001g0171a0001c0001t0002g0159a0002c0003t0001g0007others(49): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6+83A>G | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 2/27 | chr2 | 17752895 | ||||||
chr2:17753137
|
A | G | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0027 | 3 | NA18946.hp1 NA18968.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-92-73T>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753137 | ||||||
chr2:17753290
|
G | T | 1 | a0001c0001t0003g0041 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-92-226C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753290 | ||||||
chr2:17753324
|
T | TGGGGACG others(11): Show |
22 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 26 | HG00735.hp2 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-92-278_-92-261dup others(18): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753324
|
T | TGGGGACG others(29): Show |
39 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0171others(36): Show | 41 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-93+266_-92-261dup others(36): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753324
|
T | TGGGGACG others(47): Show |
28 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176others(25): Show | 29 | HG00140.hp2 HG00621.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-92-261_-92-260ins others(54): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753324
|
T | TGGGGACG others(65): Show |
37 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0214others(34): Show | 37 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-92-261_-92-260ins others(72): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753324
|
T | TGGGGACG others(83): Show |
10 | a0001c0001t0002g0187a0001c0001t0002g0226a0001c0001t0002g0227others(7): Show | 10 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.-92-261_-92-260ins others(90): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753324
|
T | TGGGGACG others(101): Show |
2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-92-261_-92-260ins others(108): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753324 | ||||||
chr2:17753407
|
C | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(24): Show | 30 | HG00621.hp1 HG00639.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+219G>C | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753407 | ||||||
chr2:17753428
|
G | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(3): Show | 7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+198C>A | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753428 | ||||||
chr2:17753453
|
C | A | 11 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0236others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+173G>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753453 | ||||||
chr2:17753559
|
AAGG | A | 14 | a0003c0002t0001g0009a0003c0002t0001g0189a0003c0002t0001g0190others(11): Show | 15 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-93+64_-93+66delCC others(1): Show |
SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753559 | ||||||
chr2:17753564
|
G | A | 30 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(27): Show | 30 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+62C>T | SMC6 | ENSG00000163029.16 | transcript | ENST00000448223.7 | protein_coding | 1/27 | chr2 | 17753564 |