geneid | 22883 |
---|---|
ensemblid | ENSG00000171603.18 |
hgncid | 17447 |
symbol | CLSTN1 |
name | calsyntenin 1 |
refseq_nuc | NM_001009566.3 |
refseq_prot | NP_001009566.1 |
ensembl_nuc | ENST00000377298.9 |
ensembl_prot | ENSP00000366513.4 |
mane_status | MANE Select |
chr | chr1 |
start | 9728926 |
end | 9823965 |
strand | - |
ver | v1.2 |
region | chr1:9728926-9823965 |
region5000 | chr1:9723926-9828965 |
regionname0 | CLSTN1_chr1_9728926_9823965 |
regionname5000 | CLSTN1_chr1_9723926_9828965 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 981 | 175 | 57 | 44 | 52 | 6 | 14 | 31 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002 | 0/0 | 981 | 78 | 23 | 10 | 32 | 2 | 11 | 27 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0003 | 0/0 | 981 | 8 | 0 | 1 | 7 | 0 | 0 | 6 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0004 | 0/0 | 981 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0005 | 0/0 | 123 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0006 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0007 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0008 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0009 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0010 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0011 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2946 | 139 | 30 | 39 | 48 | 6 | 14 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0002 | 0/0 | 2946 | 74 | 22 | 10 | 29 | 2 | 11 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0003 | 0/0 | 2946 | 30 | 25 | 4 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0004 | 0/0 | 2946 | 8 | 0 | 1 | 7 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0005 | 0/0 | 2946 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0006 | 0/0 | 2946 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0007 | 0/0 | 2946 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0008 | 0/0 | 2946 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0009 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0010 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0011 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0012 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0013 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0014 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0015 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0016 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0017 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0018 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
c0019 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1815 | 136 | 26 | 40 | 49 | 6 | 14 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0002 | 0/0 | 1815 | 65 | 25 | 9 | 25 | 2 | 4 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0003 | 0/0 | 1815 | 21 | 0 | 3 | 12 | 0 | 6 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0004 | 0/0 | 1815 | 19 | 17 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0005 | 0/0 | 1815 | 6 | 6 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0006 | 0/0 | 1815 | 5 | 2 | 2 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0007 | 0/0 | 1825 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0008 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0009 | 0/0 | 1890 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0010 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0011 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0012 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0013 | 1/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0014 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0015 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0016 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0017 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0018 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0019 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0020 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
t0021 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2946 | 139 | 30 | 39 | 48 | 6 | 14 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0003 | 0/0 | 2946 | 30 | 25 | 4 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0006 | 0/0 | 2946 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0008 | 0/0 | 2946 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0014 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0016 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002 | 0/0 | 2946 | 74 | 22 | 10 | 29 | 2 | 11 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0007 | 0/0 | 2946 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0010 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0019 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0003c0004 | 0/0 | 2946 | 8 | 0 | 1 | 7 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0004c0005 | 0/0 | 2946 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0005c0011 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0006c0015 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0007c0017 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0008c0013 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0009c0012 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0010c0018 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0011c0009 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4760 | 129 | 25 | 38 | 46 | 6 | 13 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0004 | 0/0 | 4760 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0008 | 0/0 | 4760 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0013 | 1/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0015 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0016 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0018 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0019 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0001t0020 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0003t0004 | 0/0 | 4760 | 17 | 15 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0003t0005 | 0/0 | 4760 | 6 | 6 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0003t0006 | 0/0 | 4760 | 5 | 2 | 2 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0003t0007 | 0/0 | 4770 | 2 | 2 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0006t0009 | 0/0 | 4835 | 2 | 1 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0008t0001 | 0/0 | 4760 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0014t0001 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0001c0016t0001 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002t0002 | 0/0 | 4760 | 51 | 22 | 8 | 15 | 2 | 4 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002t0003 | 0/0 | 4760 | 20 | 0 | 2 | 12 | 0 | 6 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002t0011 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002t0012 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0002t0017 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0007t0002 | 0/0 | 4760 | 2 | 0 | 0 | 2 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0010t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0002c0019t0002 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0003c0004t0002 | 0/0 | 4760 | 8 | 0 | 1 | 7 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0004c0005t0001 | 0/0 | 4760 | 2 | 0 | 2 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0005c0011t0021 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0006c0015t0014 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0007c0017t0010 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0008c0013t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0009c0012t0003 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0010c0018t0001 | 0/0 | 4760 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
a0011c0009t0002 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | copy fasta | chr1 | 9723926 | 9828965 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0013g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0015g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0016g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0018g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0019g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0003t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0006t0009g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0006t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0014t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0001c0016t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0002t0017g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0007t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0007t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0010t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0002c0019t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0003c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0004c0005t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0004c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0005c0011t0021g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0006c0015t0014g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0007c0017t0010g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0008c0013t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0009c0012t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0010c0018t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
a0011c0009t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00558 | hp1 | a0003 | c0004 | t0002 | g0070 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00558 | hp2 | a0005 | c0011 | t0021 | g0270 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00733 | hp2 | a0001 | c0003 | t0004 | g0114 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0058 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01109 | hp1 | a0001 | c0003 | t0004 | g0261 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01243 | hp2 | a0001 | c0006 | t0009 | g0266 | AMR | PUR | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01255 | hp1 | a0001 | c0003 | t0006 | g0055 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0084 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01258 | hp2 | a0004 | c0005 | t0001 | g0212 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01261 | hp2 | a0009 | c0012 | t0003 | g0036 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0086 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0102 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0101 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01884 | hp1 | a0008 | c0013 | t0002 | g0013 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01884 | hp2 | a0007 | c0017 | t0010 | g0001 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01891 | hp1 | a0011 | c0009 | t0002 | g0002 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0118 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01981 | hp2 | a0003 | c0004 | t0002 | g0063 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02004 | hp1 | a0004 | c0005 | t0001 | g0211 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02004 | hp2 | a0001 | c0001 | t0015 | g0237 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02027 | hp2 | a0001 | c0008 | t0001 | g0135 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02071 | hp1 | a0001 | c0016 | t0001 | g0145 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02083 | hp1 | a0002 | c0002 | t0011 | g0053 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02083 | hp2 | a0001 | c0003 | t0006 | g0096 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0083 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02258 | hp1 | a0001 | c0003 | t0006 | g0035 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02280 | hp1 | a0001 | c0003 | t0005 | g0099 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02280 | hp2 | a0001 | c0014 | t0001 | g0253 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02293 | hp2 | a0001 | c0003 | t0006 | g0046 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02451 | hp1 | a0001 | c0003 | t0004 | g0113 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | KHV | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02615 | hp1 | a0001 | c0003 | t0004 | g0116 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02615 | hp2 | a0001 | c0003 | t0005 | g0100 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02647 | hp2 | a0001 | c0003 | t0004 | g0119 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0033 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0240 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02723 | hp2 | a0001 | c0003 | t0005 | g0098 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02897 | hp2 | a0001 | c0003 | t0004 | g0111 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02970 | hp2 | a0001 | c0006 | t0009 | g0267 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03041 | hp2 | a0001 | c0003 | t0004 | g0123 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03139 | hp1 | a0001 | c0003 | t0007 | g0095 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0122 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03453 | hp2 | a0001 | c0003 | t0004 | g0112 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03486 | hp1 | a0001 | c0003 | t0004 | g0110 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0049 | SAS | PJL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ESN | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03540 | hp1 | a0001 | c0001 | t0020 | g0269 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | GWD | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03579 | hp2 | a0001 | c0003 | t0007 | g0037 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0042 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03834 | hp1 | a0010 | c0018 | t0001 | g0234 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03834 | hp2 | a0001 | c0001 | t0016 | g0259 | SAS | BEB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0073 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0034 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04204 | hp2 | a0002 | c0002 | t0017 | g0107 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0108 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18940 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18940 | hp2 | a0003 | c0004 | t0002 | g0064 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18948 | hp1 | a0001 | c0001 | t0019 | g0168 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18951 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18963 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18964 | hp1 | a0001 | c0008 | t0001 | g0214 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18968 | hp2 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18971 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18983 | hp2 | a0003 | c0004 | t0002 | g0069 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18985 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18990 | hp1 | a0003 | c0004 | t0002 | g0068 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18995 | hp2 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18999 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19000 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19005 | hp1 | a0002 | c0019 | t0002 | g0060 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19030 | hp1 | a0002 | c0010 | t0002 | g0038 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19043 | hp1 | a0001 | c0003 | t0005 | g0097 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19064 | hp1 | a0001 | c0001 | t0018 | g0173 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19066 | hp1 | a0002 | c0007 | t0002 | g0087 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19079 | hp2 | a0002 | c0002 | t0012 | g0090 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19080 | hp2 | a0002 | c0007 | t0002 | g0076 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19082 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19082 | hp2 | a0003 | c0004 | t0002 | g0066 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | GIH | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0029 | AMR | CLM | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02486 | hp2 | a0001 | c0003 | t0006 | g0056 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02559 | hp1 | a0001 | c0003 | t0004 | g0117 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | ACB | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0115 | AFR | MSL | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG06807 | hp1 | a0001 | c0003 | t0004 | g0120 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | USA | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
NA21309 | hp2 | a0006 | c0015 | t0014 | g0103 | AFR | LWK | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0258 | REF | REF | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0104 | REF | REF | CLSTN1_chr1_9723926_9828965 | CLSTN1 | chr1 | 9723926 | 9828965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9730584
|
T | C | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2870A>G | p.Glu957Gly | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3102/4760 | 2870/2946 | 957/981 | chr1 | 9730584 | ||
chr1:9730601
|
C | G | 1 | a0009 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.2853G>C | p.Glu951Asp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3085/4760 | 2853/2946 | 951/981 | chr1 | 9730601 | ||
chr1:9743997
|
G | A | 1 | a0007 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1243C>T | p.Arg415Trp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/19 | 1475/4760 | 1243/2946 | 415/981 | chr1 | 9743997 | ||
chr1:9744634
|
G | A | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.995C>T | p.Ala332Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1227/4760 | 995/2946 | 332/981 | chr1 | 9744634 | ||
chr1:9744635
|
C | T | 4 | a0002a0008a0009others(1): Show | 81 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(78): Show |
missense_variant | MODERATE | c.994G>A | p.Ala332Thr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1226/4760 | 994/2946 | 332/981 | chr1 | 9744635 | ||
chr1:9744640
|
G | A | 1 | a0010 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.989C>T | p.Ala330Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/19 | 1221/4760 | 989/2946 | 330/981 | chr1 | 9744640 | ||
chr1:9751595
|
C | T | 1 | a0004 | 2 | HG01258.hp2 HG02004.hp1 |
missense_variant | MODERATE | c.527G>A | p.Gly176Glu | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 759/4760 | 527/2946 | 176/981 | chr1 | 9751595 | ||
chr1:9755182
|
A | C | 1 | a0005 | 1 | HG00558.hp2 | stop_gained | HIGH | c.372T>G | p.Tyr124* | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/19 | 604/4760 | 372/2946 | 124/981 | chr1 | 9755182 | ||
chr1:9773277
|
A | T | 1 | a0003 | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
missense_variant | MODERATE | c.209T>A | p.Phe70Tyr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/19 | 441/4760 | 209/2946 | 70/981 | chr1 | 9773277 | ||
chr1:9823712
|
C | T | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.22G>A | p.Ala8Thr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 254/4760 | 22/2946 | 8/981 | chr1 | 9823712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9730568
|
G | A | 1 | a0001c0014 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2886C>T | p.Asp962Asp | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 3118/4760 | 2886/2946 | 962/981 | chr1 | 9730568 | ||
chr1:9731894
|
C | T | 1 | a0001c0016 | 1 | HG02071.hp1 | splice_region_variant&synonymous_variant | LOW | c.2430G>A | p.Val810Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/19 | 2662/4760 | 2430/2946 | 810/981 | chr1 | 9731894 | ||
chr1:9749561
|
T | C | 1 | a0001c0008 | 2 | HG02027.hp2 NA18964.hp1 |
synonymous_variant | LOW | c.885A>G | p.Pro295Pro | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/19 | 1117/4760 | 885/2946 | 295/981 | chr1 | 9749561 | ||
chr1:9749618
|
C | T | 1 | a0001c0006 | 2 | HG01243.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.828G>A | p.Pro276Pro | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/19 | 1060/4760 | 828/2946 | 276/981 | chr1 | 9749618 | ||
chr1:9749882
|
G | A | 1 | a0002c0007 | 2 | NA19066.hp1 NA19080.hp2 |
synonymous_variant | LOW | c.681C>T | p.Tyr227Tyr | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 6/19 | 913/4760 | 681/2946 | 227/981 | chr1 | 9749882 | ||
chr1:9751483
|
A | G | 12 | a0001c0003a0001c0006a0001c0014others(9): Show | 123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
synonymous_variant | LOW | c.639T>C | p.Val213Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 871/4760 | 639/2946 | 213/981 | chr1 | 9751483 | ||
chr1:9751600
|
G | A | 1 | a0002c0019 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.522C>T | p.Ile174Ile | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/19 | 754/4760 | 522/2946 | 174/981 | chr1 | 9751600 | ||
chr1:9773393
|
A | G | 1 | a0002c0010 | 1 | NA19030.hp1 | splice_region_variant&synonymous_variant | LOW | c.93T>C | p.Val31Val | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/19 | 325/4760 | 93/2946 | 31/981 | chr1 | 9773393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9729092
|
C | T | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1416G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1416 | chr1 | 9729092 | |||||
chr1:9729142
|
G | A | 1 | a0006c0015t0014 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1366 | chr1 | 9729142 | |||||
chr1:9729410
|
C | G | 1 | a0001c0001t0008 | 2 | HG02647.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1098G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 1098 | chr1 | 9729410 | |||||
chr1:9729519
|
G | A | 4 | a0002c0002t0003a0002c0002t0011a0002c0002t0017others(1): Show | 23 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*989C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 989 | chr1 | 9729519 | |||||
chr1:9729523
|
C | A | 1 | a0001c0001t0016 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 985 | chr1 | 9729523 | |||||
chr1:9729544
|
C | CCAAAAGG others(68): Show |
1 | a0001c0006t0009 | 2 | HG01243.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*889_*963dupCTTAAA others(69): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 963 | chr1 | 9729544 | |||||
chr1:9729833
|
T | C | 18 | a0001c0001t0004a0001c0003t0004a0001c0003t0005others(15): Show | 119 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*675A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 675 | chr1 | 9729833 | |||||
chr1:9729837
|
C | G | 1 | a0002c0002t0012 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 671 | chr1 | 9729837 | |||||
chr1:9729855
|
G | GGGGCGGG others(3): Show |
1 | a0001c0003t0007 | 2 | HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643_*652dupAGCCCC others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 652 | chr1 | 9729855 | |||||
chr1:9729911
|
G | A | 1 | a0001c0001t0018 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 597 | chr1 | 9729911 | |||||
chr1:9730027
|
T | C | 1 | a0001c0001t0019 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 481 | chr1 | 9730027 | |||||
chr1:9730194
|
G | C | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*314C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 314 | chr1 | 9730194 | |||||
chr1:9730220
|
G | A | 1 | a0001c0003t0005 | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*288C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 288 | chr1 | 9730220 | |||||
chr1:9730305
|
C | T | 1 | a0002c0002t0011 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 203 | chr1 | 9730305 | |||||
chr1:9730322
|
C | T | 1 | a0005c0011t0021 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 186 | chr1 | 9730322 | |||||
chr1:9730362
|
C | T | 1 | a0001c0001t0015 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 19/19 | 146 | chr1 | 9730362 | |||||
chr1:9823805
|
C | A | 1 | a0001c0001t0020 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 72 | chr1 | 9823805 | |||||
chr1:9823820
|
T | C | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(29): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | chr1 | 9823820 | ||||||
chr1:9823902
|
A | G | 14 | a0001c0003t0005a0001c0003t0006a0001c0003t0007others(11): Show | 101 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(98): Show |
5_prime_UTR_variant | MODIFIER | c.-169T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 169 | chr1 | 9823902 | |||||
chr1:9823920
|
C | T | 1 | a0007c0017t0010 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 187 | chr1 | 9823920 | |||||
chr1:9823930
|
C | A | 1 | a0005c0011t0021 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-197G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/19 | 197 | chr1 | 9823930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9730730
|
A | G | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2749-25T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730730 | ||||||
chr1:9730738
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2749-33C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730738 | ||||||
chr1:9730825
|
G | A | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2749-120C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730825 | ||||||
chr1:9730841
|
C | T | 19 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(16): Show | 19 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.2749-136G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730841 | ||||||
chr1:9730848
|
G | A | 1 | a0002c0002t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2749-143C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730848 | ||||||
chr1:9730903
|
C | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2749-198G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730903 | ||||||
chr1:9730904
|
A | G | 10 | a0001c0001t0004g0183a0001c0001t0004g0219a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2749-199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730904 | ||||||
chr1:9730937
|
A | G | 200 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.2749-232T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730937 | ||||||
chr1:9730958
|
T | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2748+248A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 18/18 | chr1 | 9730958 | ||||||
chr1:9731404
|
AG | A | 10 | a0001c0001t0004g0183a0001c0001t0004g0219a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2564-15delC | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731404 | ||||||
chr1:9731428
|
G | A | 18 | a0001c0003t0004g0261a0001c0003t0005g0008a0001c0003t0005g0009others(15): Show | 18 | HG00558.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2564-38C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731428 | ||||||
chr1:9731488
|
C | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2564-98G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731488 | ||||||
chr1:9731559
|
G | A | 1 | a0001c0003t0006g0046 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2564-169C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731559 | ||||||
chr1:9731581
|
G | A | 89 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(86): Show | 89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.2563+180C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 17/18 | chr1 | 9731581 | ||||||
chr1:9731920
|
G | A | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2428-24C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9731920 | ||||||
chr1:9731993
|
C | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2428-97G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9731993 | ||||||
chr1:9732026
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2428-130G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732026 | ||||||
chr1:9732027
|
G | A | 3 | a0001c0001t0004g0183a0001c0001t0004g0219a0002c0002t0003g0022 | 3 | HG02145.hp2 HG03225.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2428-131C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732027 | ||||||
chr1:9732047
|
G | GA | 269 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2428-152dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732047 | ||||||
chr1:9732157
|
T | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2428-261A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732157 | ||||||
chr1:9732491
|
G | A | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2428-595C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732491 | ||||||
chr1:9732503
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2428-607C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732503 | ||||||
chr1:9732579
|
T | C | 2 | a0002c0002t0002g0010a0002c0002t0002g0015 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2428-683A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732579 | ||||||
chr1:9732707
|
G | C | 12 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0006t0009g0266others(9): Show | 12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2427+694C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732707 | ||||||
chr1:9732722
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2427+679G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732722 | ||||||
chr1:9732756
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.2427+645T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732756 | ||||||
chr1:9732794
|
C | T | 1 | a0001c0001t0008g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2427+607G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9732794 | ||||||
chr1:9733027
|
A | AAAAT | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2427+370_2427+373d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733027 | ||||||
chr1:9733158
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2427+243C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733158 | ||||||
chr1:9733246
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2427+155G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733246 | ||||||
chr1:9733300
|
A | G | 12 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0006t0009g0266others(9): Show | 12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2427+101T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733300 | ||||||
chr1:9733394
|
T | A | 29 | a0002c0002t0002g0043a0002c0002t0002g0047a0002c0002t0002g0059others(26): Show | 29 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2427+7A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 16/18 | chr1 | 9733394 | ||||||
chr1:9733601
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2282-55G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733601 | ||||||
chr1:9733787
|
T | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2281+185A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733787 | ||||||
chr1:9733865
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2281+107A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733865 | ||||||
chr1:9733960
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2281+12G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 15/18 | chr1 | 9733960 | ||||||
chr1:9734198
|
C | T | 1 | a0002c0002t0003g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2111-56G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734198 | ||||||
chr1:9734208
|
T | C | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2111-66A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734208 | ||||||
chr1:9734225
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2111-83G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734225 | ||||||
chr1:9734247
|
C | T | 118 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0003t0004g0108others(115): Show | 118 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(115): Show |
intron_variant | MODIFIER | c.2111-105G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734247 | ||||||
chr1:9734281
|
C | T | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2111-139G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734281 | ||||||
chr1:9734419
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2111-277T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734419 | ||||||
chr1:9734574
|
C | CAAAA | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.2110+370_2110+373d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734574 | ||||||
chr1:9734589
|
A | G | 18 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2110+359T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734589 | ||||||
chr1:9734614
|
G | C | 1 | a0002c0002t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2110+334C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734614 | ||||||
chr1:9734640
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2110+308G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734640 | ||||||
chr1:9734924
|
C | T | 89 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(86): Show | 89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.2110+24G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734924 | ||||||
chr1:9734937
|
G | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0164others(2): Show | 5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2110+11C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 14/18 | chr1 | 9734937 | ||||||
chr1:9735192
|
G | A | 89 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(86): Show | 89 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(86): Show |
intron_variant | MODIFIER | c.1884-18C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 13/18 | chr1 | 9735192 | ||||||
chr1:9735318
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1884-144G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 13/18 | chr1 | 9735318 | ||||||
chr1:9735652
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1735-37C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735652 | ||||||
chr1:9735661
|
C | T | 119 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0003t0004g0108others(116): Show | 119 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.1735-46G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735661 | ||||||
chr1:9735847
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+38C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735847 | ||||||
chr1:9735861
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+24C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 12/18 | chr1 | 9735861 | ||||||
chr1:9736125
|
G | A | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577-83C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736125 | ||||||
chr1:9736280
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1577-238G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736280 | ||||||
chr1:9736473
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1577-431C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736473 | ||||||
chr1:9736651
|
G | A | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1577-609C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736651 | ||||||
chr1:9736756
|
A | G | 24 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0073others(21): Show | 24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1577-714T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736756 | ||||||
chr1:9736937
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1576+561C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736937 | ||||||
chr1:9736965
|
T | C | 12 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0006t0009g0266others(9): Show | 12 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1576+533A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736965 | ||||||
chr1:9736968
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576+530C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9736968 | ||||||
chr1:9737094
|
C | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1576+404G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737094 | ||||||
chr1:9737203
|
C | CT | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576+294dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737203 | ||||||
chr1:9737258
|
TG | T | 201 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126others(198): Show | 201 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1576+239delC | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737258 | ||||||
chr1:9737262
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576+236C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 11/18 | chr1 | 9737262 | ||||||
chr1:9737657
|
A | G | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520-103T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737657 | ||||||
chr1:9737788
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0008g0141a0001c0001t0008g0240 | 3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1520-234G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737788 | ||||||
chr1:9737859
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1520-305G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737859 | ||||||
chr1:9737996
|
A | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520-442T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9737996 | ||||||
chr1:9738009
|
A | G | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520-455T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738009 | ||||||
chr1:9738041
|
C | A | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1520-487G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738041 | ||||||
chr1:9738041
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1520-487G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738041 | ||||||
chr1:9738123
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520-569T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738123 | ||||||
chr1:9738188
|
T | G | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1520-634A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738188 | ||||||
chr1:9738409
|
G | C | 24 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0073others(21): Show | 24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1520-855C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738409 | ||||||
chr1:9738451
|
G | C | 2 | a0004c0005t0001g0211a0004c0005t0001g0212 | 2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1520-897C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738451 | ||||||
chr1:9738833
|
G | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1520-1279C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738833 | ||||||
chr1:9738836
|
G | A | 120 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0003t0004g0108others(117): Show | 120 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.1520-1282C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738836 | ||||||
chr1:9738904
|
C | T | 3 | a0003c0004t0002g0064a0003c0004t0002g0066a0003c0004t0002g0067 | 3 | NA18940.hp2 NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1520-1350G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738904 | ||||||
chr1:9738916
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1520-1362A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738916 | ||||||
chr1:9738949
|
G | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1520-1395C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738949 | ||||||
chr1:9738996
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1520-1442A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9738996 | ||||||
chr1:9739310
|
C | T | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1520-1756G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739310 | ||||||
chr1:9739328
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1519+1766G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739328 | ||||||
chr1:9739438
|
G | C | 76 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1519+1656C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739438 | ||||||
chr1:9739606
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1519+1488C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739606 | ||||||
chr1:9739610
|
G | A | 38 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1519+1484C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739610 | ||||||
chr1:9739635
|
G | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1519+1459C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739635 | ||||||
chr1:9739752
|
G | C | 5 | a0002c0002t0003g0030a0002c0002t0003g0031a0002c0002t0003g0050others(2): Show | 5 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1519+1342C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739752 | ||||||
chr1:9739766
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1519+1328A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739766 | ||||||
chr1:9739794
|
G | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1519+1300C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739794 | ||||||
chr1:9739814
|
A | AT | 12 | a0001c0001t0001g0106a0001c0001t0001g0137a0001c0001t0001g0150others(9): Show | 12 | HG00140.hp2 HG00735.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1519+1279dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | ||||||
chr1:9739814
|
AT | A | 97 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0001g0197others(94): Show | 97 | HG00423.hp2 HG00558.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1519+1279delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | ||||||
chr1:9739814
|
ATT | A | 21 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(18): Show | 21 | HG00733.hp2 HG01891.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1519+1278_1519+127 others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739814 | ||||||
chr1:9739817
|
T | C | 1 | a0001c0006t0009g0267 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1519+1277A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739817 | ||||||
chr1:9739818
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+1276A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739818 | ||||||
chr1:9739845
|
T | C | 123 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0003t0004g0108others(120): Show | 123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.1519+1249A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739845 | ||||||
chr1:9739977
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+1117A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9739977 | ||||||
chr1:9740083
|
T | G | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1519+1011A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740083 | ||||||
chr1:9740112
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1519+982C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740112 | ||||||
chr1:9740124
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0218a0001c0001t0001g0222others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519+970T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740124 | ||||||
chr1:9740187
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1519+907C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740187 | ||||||
chr1:9740349
|
C | T | 7 | a0002c0002t0002g0007a0002c0002t0002g0024a0002c0002t0002g0025others(4): Show | 7 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519+745G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740349 | ||||||
chr1:9740350
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+744C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740350 | ||||||
chr1:9740493
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519+601T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740493 | ||||||
chr1:9740529
|
T | C | 1 | a0008c0013t0002g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1519+565A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740529 | ||||||
chr1:9740679
|
C | T | 4 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0006t0009g0266others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+415G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740679 | ||||||
chr1:9740722
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1519+372G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9740722 | ||||||
chr1:9741063
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+31G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 10/18 | chr1 | 9741063 | ||||||
chr1:9741283
|
G | A | 72 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(69): Show | 72 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(69): Show |
intron_variant | MODIFIER | c.1357-27C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741283 | ||||||
chr1:9741447
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1357-191C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741447 | ||||||
chr1:9741451
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357-195C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741451 | ||||||
chr1:9741480
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-224C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741480 | ||||||
chr1:9741649
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG00738.hp2 HG01517.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-393C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741649 | ||||||
chr1:9741703
|
A | G | 123 | a0001c0001t0004g0183a0001c0001t0004g0219a0001c0003t0004g0108others(120): Show | 123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.1357-447T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741703 | ||||||
chr1:9741817
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1357-561G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741817 | ||||||
chr1:9741921
|
G | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1357-665C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741921 | ||||||
chr1:9741938
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1357-682A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741938 | ||||||
chr1:9741969
|
A | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1357-713T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9741969 | ||||||
chr1:9742000
|
A | G | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1357-744T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742000 | ||||||
chr1:9742195
|
G | A | 1 | a0002c0002t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1357-939C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742195 | ||||||
chr1:9742277
|
T | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0164others(2): Show | 5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357-1021A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742277 | ||||||
chr1:9742336
|
C | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357-1080G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742336 | ||||||
chr1:9742348
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357-1092C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742348 | ||||||
chr1:9742355
|
T | C | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357-1099A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742355 | ||||||
chr1:9742680
|
A | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1356+1204T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742680 | ||||||
chr1:9742730
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+1154C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742730 | ||||||
chr1:9742761
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+1123T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742761 | ||||||
chr1:9742764
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1356+1120G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742764 | ||||||
chr1:9742777
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1356+1107C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742777 | ||||||
chr1:9742883
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1356+1001C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742883 | ||||||
chr1:9742919
|
A | G | 11 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1356+965T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742919 | ||||||
chr1:9742964
|
A | G | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1356+920T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9742964 | ||||||
chr1:9743145
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1356+739G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743145 | ||||||
chr1:9743369
|
G | A | 1 | a0001c0001t0016g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1356+515C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743369 | ||||||
chr1:9743499
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1356+385G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743499 | ||||||
chr1:9743536
|
A | G | 24 | a0002c0002t0002g0071a0002c0002t0002g0072a0002c0002t0002g0073others(21): Show | 24 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1356+348T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743536 | ||||||
chr1:9743570
|
C | T | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1356+314G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743570 | ||||||
chr1:9743604
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1356+280C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743604 | ||||||
chr1:9743664
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1356+220G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743664 | ||||||
chr1:9743724
|
G | GT | 26 | a0001c0001t0001g0167a0001c0001t0001g0223a0001c0001t0001g0263others(23): Show | 26 | HG00423.hp1 HG00733.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.1356+159dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743724 | ||||||
chr1:9743724
|
G | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0205 | 2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1356+160C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743724 | ||||||
chr1:9743786
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1356+98C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 9/18 | chr1 | 9743786 | ||||||
chr1:9744094
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1235-89T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744094 | ||||||
chr1:9744128
|
C | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-123G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744128 | ||||||
chr1:9744190
|
G | A | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-185C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744190 | ||||||
chr1:9744196
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-191G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744196 | ||||||
chr1:9744257
|
C | T | 2 | a0004c0005t0001g0211a0004c0005t0001g0212 | 2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1234+138G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744257 | ||||||
chr1:9744268
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1234+127G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744268 | ||||||
chr1:9744312
|
T | C | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234+83A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 8/18 | chr1 | 9744312 | ||||||
chr1:9744661
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986-18C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744661 | ||||||
chr1:9744672
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.986-29A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744672 | ||||||
chr1:9744696
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-53T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744696 | ||||||
chr1:9744775
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-132C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744775 | ||||||
chr1:9744973
|
G | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-330C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9744973 | ||||||
chr1:9745132
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-489C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745132 | ||||||
chr1:9745145
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.986-502G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745145 | ||||||
chr1:9745216
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-573C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745216 | ||||||
chr1:9745228
|
CA | C | 108 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.986-586delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745228 | ||||||
chr1:9745228
|
CAA | C | 79 | a0001c0001t0001g0151a0001c0001t0001g0224a0001c0001t0004g0183others(76): Show | 79 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.986-587_986-586del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745228 | ||||||
chr1:9745351
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-708C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745351 | ||||||
chr1:9745380
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-737C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745380 | ||||||
chr1:9745396
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-753G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745396 | ||||||
chr1:9745636
|
G | A | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.986-993C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745636 | ||||||
chr1:9745694
|
T | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.986-1051A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745694 | ||||||
chr1:9745765
|
G | GT | 54 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0137others(51): Show | 54 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.986-1123dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | ||||||
chr1:9745765
|
G | GTT | 7 | a0001c0001t0001g0154a0001c0001t0001g0217a0001c0001t0001g0227others(4): Show | 7 | HG00733.hp1 HG01981.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-1124_986-1123d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | ||||||
chr1:9745765
|
GT | G | 60 | a0001c0001t0001g0210a0001c0001t0001g0255a0001c0001t0001g0262others(57): Show | 60 | HG00423.hp2 HG00639.hp1 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.986-1123delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745765 | ||||||
chr1:9745846
|
G | A | 2 | a0002c0007t0002g0076a0002c0007t0002g0087 | 2 | NA19066.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.986-1203C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745846 | ||||||
chr1:9745915
|
T | C | 2 | a0001c0003t0006g0055a0001c0003t0006g0056 | 2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.986-1272A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745915 | ||||||
chr1:9745931
|
G | A | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.986-1288C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9745931 | ||||||
chr1:9746293
|
T | A | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.986-1650A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746293 | ||||||
chr1:9746359
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-1716C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746359 | ||||||
chr1:9746453
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0227 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.986-1810G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746453 | ||||||
chr1:9746527
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-1884G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746527 | ||||||
chr1:9746566
|
G | T | 248 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.986-1923C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746566 | ||||||
chr1:9746618
|
G | A | 6 | a0002c0002t0002g0007a0002c0002t0002g0024a0002c0002t0002g0025others(3): Show | 6 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.986-1975C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746618 | ||||||
chr1:9746886
|
T | C | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-2243A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746886 | ||||||
chr1:9746963
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.986-2320A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9746963 | ||||||
chr1:9747095
|
G | A | 1 | a0002c0002t0002g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.985+2366C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747095 | ||||||
chr1:9747126
|
G | A | 2 | a0001c0003t0005g0097a0001c0003t0005g0098 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.985+2335C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747126 | ||||||
chr1:9747135
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985+2326G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747135 | ||||||
chr1:9747176
|
C | CA | 21 | a0001c0001t0001g0152a0001c0001t0001g0167a0001c0001t0001g0170others(18): Show | 21 | HG00558.hp2 HG01258.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.985+2284dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
C | CAAAAAAA others(8): Show |
2 | a0003c0004t0002g0063a0003c0004t0002g0069 | 2 | HG01981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.985+2270_985+2284d others(17): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
C | CAAAAAAA others(9): Show |
1 | a0003c0004t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.985+2269_985+2284d others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
C | CAAAAAAA others(11): Show |
2 | a0003c0004t0002g0067a0003c0004t0002g0068 | 2 | NA18968.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.985+2267_985+2284d others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
C | CAAAAAAA others(16): Show |
1 | a0003c0004t0002g0064 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.985+2262_985+2284d others(25): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
C | CAAAAAAA others(21): Show |
1 | a0003c0004t0002g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.985+2284_985+2285i others(30): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
CA | C | 68 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0156others(65): Show | 68 | HG00423.hp2 HG01081.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.985+2284delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
CAA | C | 8 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(5): Show | 8 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+2283_985+2284d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747176
|
CAAAAAA | C | 13 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(10): Show | 13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.985+2279_985+2284d others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747176 | ||||||
chr1:9747222
|
G | A | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.985+2239C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747222 | ||||||
chr1:9747253
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+2208A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747253 | ||||||
chr1:9747297
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.985+2164G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747297 | ||||||
chr1:9747325
|
A | G | 14 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(11): Show | 14 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.985+2136T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747325 | ||||||
chr1:9747607
|
C | A | 1 | a0002c0002t0017g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.985+1854G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747607 | ||||||
chr1:9747731
|
A | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+1730T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747731 | ||||||
chr1:9747772
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.985+1689C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747772 | ||||||
chr1:9747819
|
G | A | 7 | a0002c0002t0002g0007a0002c0002t0002g0024a0002c0002t0002g0025others(4): Show | 7 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+1642C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747819 | ||||||
chr1:9747860
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.985+1601C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747860 | ||||||
chr1:9747950
|
G | A | 1 | a0002c0010t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.985+1511C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9747950 | ||||||
chr1:9748042
|
T | TA | 32 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(29): Show | 32 | HG00733.hp2 HG01109.hp1 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.985+1418dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748042 | ||||||
chr1:9748042
|
TA | T | 9 | a0001c0001t0001g0193a0003c0004t0002g0063a0003c0004t0002g0064others(6): Show | 9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.985+1418delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748042 | ||||||
chr1:9748244
|
A | G | 122 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(119): Show | 122 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(119): Show |
intron_variant | MODIFIER | c.985+1217T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748244 | ||||||
chr1:9748400
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+1061T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748400 | ||||||
chr1:9748411
|
T | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+1050A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748411 | ||||||
chr1:9748545
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+916G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748545 | ||||||
chr1:9748546
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.985+915C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748546 | ||||||
chr1:9748619
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+842A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748619 | ||||||
chr1:9748679
|
G | C | 1 | a0002c0002t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.985+782C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748679 | ||||||
chr1:9748687
|
C | T | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.985+774G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748687 | ||||||
chr1:9748956
|
G | A | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.985+505C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9748956 | ||||||
chr1:9749016
|
C | CA | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+444_985+445ins others(1): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749016 | ||||||
chr1:9749017
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+444C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749017 | ||||||
chr1:9749100
|
C | T | 2 | a0002c0002t0002g0074a0002c0002t0002g0079 | 2 | HG01346.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.985+361G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749100 | ||||||
chr1:9749197
|
T | C | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.985+264A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749197 | ||||||
chr1:9749284
|
C | T | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.985+177G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 7/18 | chr1 | 9749284 | ||||||
chr1:9749988
|
C | T | 1 | a0002c0002t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.650-75G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9749988 | ||||||
chr1:9750040
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-127C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750040 | ||||||
chr1:9750226
|
T | C | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.650-313A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750226 | ||||||
chr1:9750412
|
G | A | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.650-499C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750412 | ||||||
chr1:9750458
|
C | T | 4 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(1): Show | 4 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-545G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750458 | ||||||
chr1:9750634
|
C | T | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.650-721G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750634 | ||||||
chr1:9750715
|
C | CAAAAAAA others(1): Show |
22 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262others(19): Show | 22 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.649+750_649+757dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | ||||||
chr1:9750715
|
C | CAAAAAAA others(2): Show |
91 | a0001c0001t0004g0183a0001c0003t0004g0115a0001c0003t0004g0117others(88): Show | 91 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.649+749_649+757dup others(9): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | ||||||
chr1:9750715
|
C | CAAAAAAA others(3): Show |
12 | a0001c0003t0006g0035a0001c0003t0006g0055a0001c0003t0006g0056others(9): Show | 12 | HG01255.hp1 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+748_649+757dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | ||||||
chr1:9750715
|
CA | C | 8 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0001t0001g0238others(5): Show | 8 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.649+757delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750715 | ||||||
chr1:9750909
|
C | A | 1 | a0002c0002t0003g0051 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.649+564G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9750909 | ||||||
chr1:9751019
|
C | T | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.649+454G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751019 | ||||||
chr1:9751377
|
A | G | 123 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(120): Show | 123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.649+96T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751377 | ||||||
chr1:9751428
|
C | A | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+45G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751428 | ||||||
chr1:9751458
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.649+15G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 5/18 | chr1 | 9751458 | ||||||
chr1:9751752
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-71A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9751752 | ||||||
chr1:9751856
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0218a0001c0001t0001g0222others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-175G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9751856 | ||||||
chr1:9752241
|
C | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.441-560G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752241 | ||||||
chr1:9752414
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.441-733G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752414 | ||||||
chr1:9752810
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.441-1129G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752810 | ||||||
chr1:9752835
|
C | G | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-1154G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752835 | ||||||
chr1:9752871
|
G | GTAAA | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1194_441-1191d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9752871 | ||||||
chr1:9753077
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.441-1396C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753077 | ||||||
chr1:9753132
|
C | T | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1451G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753132 | ||||||
chr1:9753187
|
C | T | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1506G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753187 | ||||||
chr1:9753210
|
C | T | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1529G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753210 | ||||||
chr1:9753211
|
G | C | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1530C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753211 | ||||||
chr1:9753341
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.441-1660G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753341 | ||||||
chr1:9753345
|
C | A | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1664G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753345 | ||||||
chr1:9753365
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0172 | 3 | HG01346.hp1 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.441-1684C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753365 | ||||||
chr1:9753424
|
T | C | 1 | a0001c0001t0019g0168 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.440+1690A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753424 | ||||||
chr1:9753493
|
A | AT | 10 | a0001c0001t0019g0168a0001c0006t0009g0266a0001c0006t0009g0267others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.440+1620dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753493 | ||||||
chr1:9753567
|
G | C | 9 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(6): Show | 9 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.440+1547C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753567 | ||||||
chr1:9753585
|
A | C | 67 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(64): Show | 67 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.440+1529T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753585 | ||||||
chr1:9753797
|
G | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.440+1317C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9753797 | ||||||
chr1:9754244
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0246 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.440+870T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754244 | ||||||
chr1:9754283
|
C | T | 1 | a0001c0016t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.440+831G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754283 | ||||||
chr1:9754341
|
G | A | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+773C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754341 | ||||||
chr1:9754491
|
G | A | 14 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(11): Show | 14 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.440+623C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754491 | ||||||
chr1:9754787
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.440+327C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754787 | ||||||
chr1:9754906
|
A | G | 128 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262others(125): Show | 128 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.440+208T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9754906 | ||||||
chr1:9755041
|
T | C | 1 | a0004c0005t0001g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.440+73A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 4/18 | chr1 | 9755041 | ||||||
chr1:9755314
|
G | A | 25 | a0001c0003t0006g0096a0002c0002t0002g0071a0002c0002t0002g0072others(22): Show | 25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.245-5C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755314 | ||||||
chr1:9755341
|
C | G | 6 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0188others(3): Show | 6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-32G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755341 | ||||||
chr1:9755485
|
C | G | 124 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262others(121): Show | 124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.245-176G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755485 | ||||||
chr1:9755555
|
G | A | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.245-246C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755555 | ||||||
chr1:9755762
|
G | GATATAGG others(12): Show |
1 | a0003c0004t0002g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.245-472_245-454dup others(19): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755762 | ||||||
chr1:9755798
|
C | CA | 246 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.245-490dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755798 | ||||||
chr1:9755798
|
C | CAA | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-491_245-490dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755798 | ||||||
chr1:9755873
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0220 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.245-564G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755873 | ||||||
chr1:9755939
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.244+542C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755939 | ||||||
chr1:9755946
|
A | C | 1 | a0001c0008t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.244+535T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755946 | ||||||
chr1:9755980
|
T | C | 1 | a0002c0002t0002g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.244+501A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755980 | ||||||
chr1:9755993
|
G | A | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+488C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9755993 | ||||||
chr1:9756062
|
A | AG | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+418_244+419ins others(1): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756062 | ||||||
chr1:9756112
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+369G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756112 | ||||||
chr1:9756214
|
T | C | 268 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.244+267A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756214 | ||||||
chr1:9756224
|
C | G | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.244+257G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756224 | ||||||
chr1:9756384
|
C | T | 1 | a0002c0002t0003g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244+97G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 3/18 | chr1 | 9756384 | ||||||
chr1:9756533
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.215-23G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756533 | ||||||
chr1:9756562
|
T | C | 269 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.215-52A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756562 | ||||||
chr1:9756563
|
G | A | 1 | a0002c0002t0002g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-53C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756563 | ||||||
chr1:9756692
|
T | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-182A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756692 | ||||||
chr1:9756709
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756709 | ||||||
chr1:9756790
|
C | CT | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-281dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9756790 | ||||||
chr1:9757008
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.215-498C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757008 | ||||||
chr1:9757019
|
C | A | 88 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(85): Show | 88 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(85): Show |
intron_variant | MODIFIER | c.215-509G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757019 | ||||||
chr1:9757205
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.215-695G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757205 | ||||||
chr1:9757211
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.215-701A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757211 | ||||||
chr1:9757244
|
G | GT | 13 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0001g0144others(10): Show | 13 | HG00423.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-735dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757244 | ||||||
chr1:9757248
|
T | TTG | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-739_215-738ins others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757248 | ||||||
chr1:9757328
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0172 | 3 | HG01346.hp1 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.215-818C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757328 | ||||||
chr1:9757537
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1027T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757537 | ||||||
chr1:9757836
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-1326G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757836 | ||||||
chr1:9757955
|
G | A | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-1445C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9757955 | ||||||
chr1:9758006
|
G | A | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-1496C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758006 | ||||||
chr1:9758006
|
G | C | 2 | a0004c0005t0001g0211a0004c0005t0001g0212 | 2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.215-1496C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758006 | ||||||
chr1:9758014
|
T | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1504A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758014 | ||||||
chr1:9758018
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1508T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758018 | ||||||
chr1:9758134
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0218a0001c0001t0001g0222others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1624G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758134 | ||||||
chr1:9758229
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.215-1719C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758229 | ||||||
chr1:9758270
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-1760C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758270 | ||||||
chr1:9758395
|
C | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-1885G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758395 | ||||||
chr1:9758441
|
G | A | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-1931C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758441 | ||||||
chr1:9758516
|
A | G | 1 | a0002c0002t0002g0043 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.215-2006T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758516 | ||||||
chr1:9758566
|
C | A | 117 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(114): Show | 117 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(114): Show |
intron_variant | MODIFIER | c.215-2056G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758566 | ||||||
chr1:9758593
|
C | T | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-2083G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758593 | ||||||
chr1:9758686
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-2176A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758686 | ||||||
chr1:9758723
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0220 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.215-2213C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758723 | ||||||
chr1:9758922
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.215-2412G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9758922 | ||||||
chr1:9759054
|
T | C | 1 | a0003c0004t0002g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.215-2544A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759054 | ||||||
chr1:9759473
|
G | A | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-2963C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759473 | ||||||
chr1:9759534
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215-3024C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759534 | ||||||
chr1:9759802
|
T | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-3292A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759802 | ||||||
chr1:9759806
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-3296A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9759806 | ||||||
chr1:9760253
|
C | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-3743G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760253 | ||||||
chr1:9760364
|
C | A | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-3854G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760364 | ||||||
chr1:9760407
|
G | A | 2 | a0002c0002t0002g0101a0002c0002t0002g0102 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.215-3897C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760407 | ||||||
chr1:9760682
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-4172C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760682 | ||||||
chr1:9760684
|
G | GT | 101 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0131others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.215-4175dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | ||||||
chr1:9760684
|
G | GTT | 40 | a0001c0001t0001g0106a0001c0001t0001g0262a0001c0003t0004g0122others(37): Show | 40 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.215-4176_215-4175d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | ||||||
chr1:9760684
|
G | GTTT | 10 | a0002c0002t0002g0027a0002c0002t0002g0071a0002c0002t0002g0072others(7): Show | 10 | HG00423.hp2 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-4177_215-4175d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | ||||||
chr1:9760684
|
GT | G | 6 | a0001c0001t0001g0185a0003c0004t0002g0064a0003c0004t0002g0065others(3): Show | 6 | HG01517.hp2 NA18940.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4175delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760684 | ||||||
chr1:9760795
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.215-4285G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760795 | ||||||
chr1:9760836
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4326A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760836 | ||||||
chr1:9760845
|
A | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-4335T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9760845 | ||||||
chr1:9761365
|
T | A | 1 | a0001c0001t0018g0173 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.215-4855A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761365 | ||||||
chr1:9761371
|
A | T | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-4861T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761371 | ||||||
chr1:9761415
|
T | C | 251 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(248): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.215-4905A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761415 | ||||||
chr1:9761506
|
TTTTTTTA others(4): Show |
T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5007_215-4997d others(13): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761506 | ||||||
chr1:9761512
|
T | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.215-5002A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761512 | ||||||
chr1:9761524
|
T | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0194 | 2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.215-5014A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761524 | ||||||
chr1:9761601
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5091A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761601 | ||||||
chr1:9761697
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-5187C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761697 | ||||||
chr1:9761705
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.215-5195C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761705 | ||||||
chr1:9761747
|
T | A | 82 | a0001c0003t0006g0096a0002c0002t0002g0003a0002c0002t0002g0004others(79): Show | 82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-5237A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761747 | ||||||
chr1:9761763
|
G | A | 1 | a0002c0002t0003g0029 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-5253C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761763 | ||||||
chr1:9761764
|
G | C | 1 | a0002c0002t0003g0029 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-5254C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761764 | ||||||
chr1:9761786
|
T | C | 1 | a0002c0002t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5276A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761786 | ||||||
chr1:9761884
|
A | G | 1 | a0002c0002t0003g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215-5374T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761884 | ||||||
chr1:9761927
|
A | G | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-5417T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761927 | ||||||
chr1:9761930
|
T | G | 1 | a0002c0002t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5420A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761930 | ||||||
chr1:9761953
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.215-5443C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761953 | ||||||
chr1:9761977
|
C | T | 1 | a0002c0002t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215-5467G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761977 | ||||||
chr1:9761984
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5474C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9761984 | ||||||
chr1:9762106
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-5596C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762106 | ||||||
chr1:9762273
|
T | C | 120 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(117): Show | 120 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.215-5763A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762273 | ||||||
chr1:9762287
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-5777G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762287 | ||||||
chr1:9762417
|
C | T | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5907G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762417 | ||||||
chr1:9762455
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-5945A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762455 | ||||||
chr1:9762460
|
CA | C | 116 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262others(113): Show | 116 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.215-5951delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762460 | ||||||
chr1:9762523
|
G | GCACTCGG others(141): Show |
16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.215-6014_215-6013i others(150): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762523 | ||||||
chr1:9762523
|
GCACTCGG others(30): Show |
G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6050_215-6014d others(39): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762523 | ||||||
chr1:9762542
|
A | ACACTCAA others(141): Show |
1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215-6033_215-6032i others(150): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762542 | ||||||
chr1:9762579
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6069C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762579 | ||||||
chr1:9762593
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6083A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762593 | ||||||
chr1:9762597
|
C | CCACTCGG others(212): Show |
2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6088_215-6087i others(221): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762597 | ||||||
chr1:9762664
|
T | C | 3 | a0003c0004t0002g0063a0003c0004t0002g0068a0003c0004t0002g0070 | 3 | HG00558.hp1 HG01981.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.215-6154A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762664 | ||||||
chr1:9762696
|
C | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6186G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762696 | ||||||
chr1:9762698
|
C | T | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.215-6188G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762698 | ||||||
chr1:9762771
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-6261G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762771 | ||||||
chr1:9762853
|
G | A | 1 | a0002c0002t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.215-6343C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762853 | ||||||
chr1:9762932
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-6422A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762932 | ||||||
chr1:9762960
|
CT | C | 82 | a0001c0003t0006g0096a0002c0002t0002g0003a0002c0002t0002g0004others(79): Show | 82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.215-6451delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9762960 | ||||||
chr1:9763075
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.215-6565G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763075 | ||||||
chr1:9763087
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.215-6577C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763087 | ||||||
chr1:9763123
|
G | A | 1 | a0002c0002t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215-6613C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763123 | ||||||
chr1:9763547
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-7037G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763547 | ||||||
chr1:9763624
|
A | T | 1 | a0002c0002t0002g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-7114T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763624 | ||||||
chr1:9763652
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.215-7142C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763652 | ||||||
chr1:9763661
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-7151A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763661 | ||||||
chr1:9763726
|
T | C | 120 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(117): Show | 120 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.215-7216A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763726 | ||||||
chr1:9763862
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-7352T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763862 | ||||||
chr1:9763866
|
A | G | 120 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(117): Show | 120 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.215-7356T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9763866 | ||||||
chr1:9764000
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-7490C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764000 | ||||||
chr1:9764102
|
AAGAAAG | A | 83 | a0001c0003t0006g0096a0002c0002t0002g0003a0002c0002t0002g0004others(80): Show | 83 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.215-7598_215-7593d others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764102 | ||||||
chr1:9764106
|
AAG | A | 25 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(22): Show | 25 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.215-7598_215-7597d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764106 | ||||||
chr1:9764198
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.215-7688A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764198 | ||||||
chr1:9764200
|
G | C | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-7690C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764200 | ||||||
chr1:9764452
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.215-7942G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764452 | ||||||
chr1:9764613
|
G | A | 38 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.215-8103C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764613 | ||||||
chr1:9764637
|
T | TA | 7 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0153others(4): Show | 7 | HG01928.hp1 HG02027.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-8128dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | ||||||
chr1:9764637
|
TA | T | 148 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(145): Show | 148 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.215-8128delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | ||||||
chr1:9764637
|
TAA | T | 30 | a0001c0001t0001g0137a0001c0001t0001g0190a0001c0001t0001g0198others(27): Show | 30 | HG00558.hp2 HG00733.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-8129_215-8128d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | ||||||
chr1:9764637
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8138_215-8128d others(13): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | ||||||
chr1:9764637
|
TAAAAAAA others(6): Show |
T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-8140_215-8128d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764637 | ||||||
chr1:9764638
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.215-8128T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764638 | ||||||
chr1:9764649
|
A | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8139T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764649 | ||||||
chr1:9764716
|
T | C | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.215-8206A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764716 | ||||||
chr1:9764830
|
A | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.215-8320T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764830 | ||||||
chr1:9764920
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+8352G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9764920 | ||||||
chr1:9765117
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+8155C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765117 | ||||||
chr1:9765240
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.214+8032G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765240 | ||||||
chr1:9765260
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.214+8012A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765260 | ||||||
chr1:9765298
|
C | A | 3 | a0001c0001t0001g0181a0001c0001t0008g0141a0001c0001t0008g0240 | 3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.214+7974G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765298 | ||||||
chr1:9765319
|
G | C | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+7953C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765319 | ||||||
chr1:9765479
|
T | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0218a0001c0001t0001g0222others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+7793A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765479 | ||||||
chr1:9765485
|
C | G | 82 | a0001c0003t0006g0096a0002c0002t0002g0003a0002c0002t0002g0004others(79): Show | 82 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(79): Show |
intron_variant | MODIFIER | c.214+7787G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765485 | ||||||
chr1:9765583
|
GA | G | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+7688delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765583 | ||||||
chr1:9765736
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+7536G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9765736 | ||||||
chr1:9766034
|
G | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+7238C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766034 | ||||||
chr1:9766046
|
G | C | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+7226C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766046 | ||||||
chr1:9766072
|
TCTAA | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+7196_214+7199d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766072 | ||||||
chr1:9766255
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+7017T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766255 | ||||||
chr1:9766430
|
G | A | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+6842C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766430 | ||||||
chr1:9766552
|
C | T | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+6720G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766552 | ||||||
chr1:9766817
|
A | T | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+6455T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766817 | ||||||
chr1:9766818
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.214+6454G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766818 | ||||||
chr1:9766886
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.214+6386C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766886 | ||||||
chr1:9766976
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.214+6296G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9766976 | ||||||
chr1:9767027
|
C | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+6245G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767027 | ||||||
chr1:9767034
|
C | T | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.214+6238G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767034 | ||||||
chr1:9767119
|
C | A | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.214+6153G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767119 | ||||||
chr1:9767143
|
A | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+6129T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767143 | ||||||
chr1:9767190
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+6082G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767190 | ||||||
chr1:9767280
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.214+5992G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767280 | ||||||
chr1:9767528
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5744C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767528 | ||||||
chr1:9767544
|
C | CA | 103 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0131others(100): Show | 103 | HG00423.hp2 HG00609.hp1 HG01081.hp1 others(100): Show |
intron_variant | MODIFIER | c.214+5727dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767544 | ||||||
chr1:9767544
|
CA | C | 10 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0226others(7): Show | 10 | HG00558.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+5727delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767544 | ||||||
chr1:9767577
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.214+5695C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767577 | ||||||
chr1:9767651
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5621T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767651 | ||||||
chr1:9767779
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+5493A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767779 | ||||||
chr1:9767805
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+5467C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767805 | ||||||
chr1:9767911
|
T | G | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214+5361A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767911 | ||||||
chr1:9767975
|
C | A | 2 | a0002c0002t0003g0048a0002c0002t0003g0054 | 2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.214+5297G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9767975 | ||||||
chr1:9768044
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+5228A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768044 | ||||||
chr1:9768265
|
T | C | 123 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(120): Show | 123 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.214+5007A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768265 | ||||||
chr1:9768308
|
C | CTGGGCGG others(24): Show |
1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+4933_214+4963d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768308 | ||||||
chr1:9768358
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4914G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768358 | ||||||
chr1:9768382
|
ATGGGGGC others(23): Show |
A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4860_214+4889d others(32): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768382 | ||||||
chr1:9768391
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214+4881C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768391 | ||||||
chr1:9768401
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.214+4871A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768401 | ||||||
chr1:9768401
|
TTGGGCGG others(23): Show |
T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+4841_214+4870d others(32): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768401 | ||||||
chr1:9768412
|
C | CA | 114 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(111): Show | 114 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(111): Show |
intron_variant | MODIFIER | c.214+4859_214+4860i others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768412 | ||||||
chr1:9768419
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.214+4853G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768419 | ||||||
chr1:9768437
|
G | A | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+4835C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768437 | ||||||
chr1:9768491
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.214+4781A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768491 | ||||||
chr1:9768498
|
T | C | 4 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(1): Show | 4 | HG01255.hp1 HG02258.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+4774A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768498 | ||||||
chr1:9768577
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+4695C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768577 | ||||||
chr1:9768586
|
C | CTGGGTGG others(25): Show |
1 | a0002c0002t0002g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.214+4685_214+4686i others(34): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | ||||||
chr1:9768586
|
C | CTGGGTGG others(24): Show |
112 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(109): Show | 112 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(109): Show |
intron_variant | MODIFIER | c.214+4655_214+4685d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | ||||||
chr1:9768586
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4686G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768586 | ||||||
chr1:9768606
|
GGGGTTCT others(24): Show |
G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4635_214+4665d others(33): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768606 | ||||||
chr1:9768667
|
CGGGGTTC others(22): Show |
C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4576_214+4604d others(31): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768667 | ||||||
chr1:9768708
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4564G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768708 | ||||||
chr1:9768715
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4557C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768715 | ||||||
chr1:9768727
|
T | C | 269 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.214+4545A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768727 | ||||||
chr1:9768728
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4544C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768728 | ||||||
chr1:9768732
|
T | TTC | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4539_214+4540i others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768732 | ||||||
chr1:9768810
|
T | C | 129 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0262others(126): Show | 129 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.214+4462A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768810 | ||||||
chr1:9768864
|
G | T | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+4408C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768864 | ||||||
chr1:9768932
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+4340C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768932 | ||||||
chr1:9768941
|
G | GAGGGAGG others(9): Show |
8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4330_214+4331i others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768941 | ||||||
chr1:9768992
|
T | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4280A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9768992 | ||||||
chr1:9769048
|
GGAGGGAG others(3): Show |
G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4214_214+4223d others(12): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769048 | ||||||
chr1:9769099
|
G | C | 2 | a0002c0007t0002g0076a0002c0007t0002g0087 | 2 | NA19066.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.214+4173C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769099 | ||||||
chr1:9769111
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4161C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769111 | ||||||
chr1:9769130
|
T | TGAGAGGG others(1): Show |
8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+4134_214+4141d others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769130 | ||||||
chr1:9769196
|
C | T | 9 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+4076G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769196 | ||||||
chr1:9769293
|
T | G | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+3979A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769293 | ||||||
chr1:9769366
|
T | C | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+3906A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769366 | ||||||
chr1:9769669
|
A | G | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+3603T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769669 | ||||||
chr1:9769785
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3487T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769785 | ||||||
chr1:9769899
|
G | A | 1 | a0002c0010t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.214+3373C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769899 | ||||||
chr1:9769903
|
T | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3369A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769903 | ||||||
chr1:9769918
|
T | G | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3354A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769918 | ||||||
chr1:9769963
|
G | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3309C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9769963 | ||||||
chr1:9770016
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3256A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770016 | ||||||
chr1:9770029
|
CA | C | 238 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.214+3242delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770029 | ||||||
chr1:9770029
|
CAA | C | 11 | a0001c0001t0001g0226a0002c0002t0002g0026a0002c0002t0002g0071others(8): Show | 11 | HG00558.hp1 HG01981.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+3241_214+3242d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770029 | ||||||
chr1:9770044
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.214+3228T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770044 | ||||||
chr1:9770151
|
T | C | 13 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(10): Show | 13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+3121A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770151 | ||||||
chr1:9770261
|
T | C | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+3011A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770261 | ||||||
chr1:9770528
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214+2744G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770528 | ||||||
chr1:9770655
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+2617A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770655 | ||||||
chr1:9770661
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.214+2611C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770661 | ||||||
chr1:9770733
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+2539G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770733 | ||||||
chr1:9770751
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+2521G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770751 | ||||||
chr1:9770769
|
G | A | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+2503C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770769 | ||||||
chr1:9770788
|
G | A | 1 | a0002c0002t0003g0029 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.214+2484C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770788 | ||||||
chr1:9770863
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.214+2409C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770863 | ||||||
chr1:9770872
|
T | C | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+2400A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770872 | ||||||
chr1:9770938
|
A | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+2334T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770938 | ||||||
chr1:9770987
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+2285G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9770987 | ||||||
chr1:9771120
|
A | G | 2 | a0002c0002t0003g0021a0002c0002t0003g0049 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.214+2152T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771120 | ||||||
chr1:9771308
|
C | T | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+1964G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771308 | ||||||
chr1:9771397
|
C | G | 5 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0001g0195others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+1875G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771397 | ||||||
chr1:9771420
|
C | A | 1 | a0002c0002t0003g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.214+1852G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771420 | ||||||
chr1:9771423
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0166others(2): Show | 5 | HG02027.hp1 HG02071.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+1849C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771423 | ||||||
chr1:9771556
|
G | C | 1 | a0002c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+1716C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771556 | ||||||
chr1:9771629
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.214+1643A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771629 | ||||||
chr1:9771641
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+1631G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771641 | ||||||
chr1:9771657
|
G | A | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.214+1615C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771657 | ||||||
chr1:9771920
|
CAT | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1350_214+1351d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771920 | ||||||
chr1:9771941
|
T | A | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+1331A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9771941 | ||||||
chr1:9772016
|
G | A | 1 | a0002c0002t0002g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214+1256C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772016 | ||||||
chr1:9772140
|
CT | C | 136 | a0001c0001t0001g0105a0001c0001t0001g0125a0001c0001t0001g0126others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.214+1131delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772140 | ||||||
chr1:9772140
|
CTT | C | 94 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0142others(91): Show | 94 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.214+1130_214+1131d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772140 | ||||||
chr1:9772166
|
T | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+1106A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772166 | ||||||
chr1:9772277
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214+995G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772277 | ||||||
chr1:9772537
|
C | T | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.214+735G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772537 | ||||||
chr1:9772635
|
A | G | 1 | a0002c0002t0002g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.214+637T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772635 | ||||||
chr1:9772836
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214+436A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772836 | ||||||
chr1:9772847
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+425G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772847 | ||||||
chr1:9772874
|
G | C | 25 | a0001c0003t0006g0096a0002c0002t0002g0071a0002c0002t0002g0072others(22): Show | 25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.214+398C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9772874 | ||||||
chr1:9773088
|
C | G | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+184G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773088 | ||||||
chr1:9773186
|
A | G | 1 | a0003c0004t0002g0069 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214+86T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773186 | ||||||
chr1:9773212
|
T | G | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.214+60A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 2/18 | chr1 | 9773212 | ||||||
chr1:9773412
|
G | C | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-18C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773412 | ||||||
chr1:9773500
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-106A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773500 | ||||||
chr1:9773676
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-282C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773676 | ||||||
chr1:9773758
|
G | C | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-364C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773758 | ||||||
chr1:9773793
|
G | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-399C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773793 | ||||||
chr1:9773863
|
G | A | 3 | a0001c0003t0004g0115a0001c0003t0004g0116a0001c0003t0004g0119 | 3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-469C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773863 | ||||||
chr1:9773870
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.92-476G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773870 | ||||||
chr1:9773899
|
A | AT | 11 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-506dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773899 | ||||||
chr1:9773977
|
A | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-583T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773977 | ||||||
chr1:9773999
|
C | G | 2 | a0001c0003t0004g0120a0001c0003t0004g0121 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-605G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9773999 | ||||||
chr1:9774045
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-651C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774045 | ||||||
chr1:9774225
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.92-831A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774225 | ||||||
chr1:9774288
|
G | A | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-894C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774288 | ||||||
chr1:9774292
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-898C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774292 | ||||||
chr1:9774334
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-940G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774334 | ||||||
chr1:9774384
|
G | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.92-990C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774384 | ||||||
chr1:9774467
|
G | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-1073C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774467 | ||||||
chr1:9774560
|
C | T | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-1166G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774560 | ||||||
chr1:9774565
|
C | CA | 8 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0001g0184others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-1172dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774565 | ||||||
chr1:9774565
|
CA | C | 9 | a0002c0002t0002g0094a0003c0004t0002g0063a0003c0004t0002g0064others(6): Show | 9 | HG00558.hp1 HG01257.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-1172delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774565 | ||||||
chr1:9774811
|
C | G | 3 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099 | 3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.92-1417G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774811 | ||||||
chr1:9774862
|
C | T | 1 | a0005c0011t0021g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.92-1468G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774862 | ||||||
chr1:9774889
|
A | C | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92-1495T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9774889 | ||||||
chr1:9775031
|
T | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-1637A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775031 | ||||||
chr1:9775312
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.92-1918C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775312 | ||||||
chr1:9775432
|
C | T | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-2038G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775432 | ||||||
chr1:9775473
|
CCT | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-2081_92-2080del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775473 | ||||||
chr1:9775559
|
A | C | 251 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(248): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.92-2165T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775559 | ||||||
chr1:9775971
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.92-2577G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775971 | ||||||
chr1:9775976
|
C | CT | 8 | a0002c0002t0002g0072a0003c0004t0002g0063a0003c0004t0002g0064others(5): Show | 8 | HG00558.hp1 HG01981.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-2583dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9775976 | ||||||
chr1:9776049
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-2655A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776049 | ||||||
chr1:9776067
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.92-2673C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776067 | ||||||
chr1:9776098
|
G | A | 9 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-2704C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776098 | ||||||
chr1:9776127
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0246 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.92-2733G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776127 | ||||||
chr1:9776172
|
C | T | 124 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(121): Show | 124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-2778G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776172 | ||||||
chr1:9776247
|
G | A | 1 | a0001c0003t0004g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2853C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776247 | ||||||
chr1:9776498
|
A | G | 124 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(121): Show | 124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-3104T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776498 | ||||||
chr1:9776524
|
T | TA | 14 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0193others(11): Show | 14 | HG00609.hp1 HG02027.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-3131dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776524 | ||||||
chr1:9776571
|
T | C | 1 | a0002c0002t0011g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.92-3177A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776571 | ||||||
chr1:9776650
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.92-3256C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776650 | ||||||
chr1:9776719
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.92-3325C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776719 | ||||||
chr1:9776788
|
C | CTCTA | 7 | a0001c0001t0001g0154a0001c0001t0001g0218a0001c0001t0001g0222others(4): Show | 7 | HG00423.hp2 HG02523.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-3398_92-3395dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776788
|
C | CTCTATCT others(1): Show |
3 | a0001c0003t0007g0037a0001c0006t0009g0266a0001c0006t0009g0267 | 3 | HG01243.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-3402_92-3395dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776788
|
C | CTCTATCT others(13): Show |
4 | a0003c0004t0002g0064a0003c0004t0002g0065a0003c0004t0002g0066others(1): Show | 4 | NA18940.hp2 NA18968.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3414_92-3395dup others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776788
|
C | CTCTATCT others(17): Show |
3 | a0003c0004t0002g0063a0003c0004t0002g0069a0003c0004t0002g0070 | 3 | HG00558.hp1 HG01981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.92-3418_92-3395dup others(24): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776788
|
C | CTCTATCT others(21): Show |
1 | a0003c0004t0002g0068 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-3395_92-3394ins others(28): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776788
|
CTCTA | C | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0002c0002t0002g0010others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3398_92-3395del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776788 | ||||||
chr1:9776807
|
T | TATCTATC others(14): Show |
1 | a0001c0003t0004g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-3434_92-3414dup others(21): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776807 | ||||||
chr1:9776845
|
CTATCATC others(10): Show |
C | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.92-3468_92-3452del others(17): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776845 | ||||||
chr1:9776862
|
T | TTATC | 93 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0125others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.92-3472_92-3469dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
T | TTATCTAT others(1): Show |
50 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0136others(47): Show | 50 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-3476_92-3469dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
T | TTATCTAT others(18): Show |
8 | a0001c0003t0004g0108a0001c0003t0004g0112a0001c0003t0004g0116others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3469_92-3468ins others(25): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
T | TTATCTAT others(22): Show |
7 | a0001c0003t0004g0109a0001c0003t0004g0110a0001c0003t0004g0111others(4): Show | 7 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-3469_92-3468ins others(29): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
T | TTATCTAT others(5): Show |
10 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0199others(7): Show | 10 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-3480_92-3469dup others(12): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
T | TTATCTAT others(9): Show |
1 | a0001c0001t0001g0208 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.92-3484_92-3469dup others(16): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
TTATC | T | 33 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(30): Show | 33 | HG00280.hp2 HG00639.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-3472_92-3469del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776862
|
TTATCTAT others(1): Show |
T | 9 | a0001c0001t0001g0182a0001c0001t0001g0221a0001c0001t0001g0226others(6): Show | 9 | HG01070.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-3476_92-3469del others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776862 | ||||||
chr1:9776974
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3580A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9776974 | ||||||
chr1:9777094
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.92-3700G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777094 | ||||||
chr1:9777155
|
G | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0163others(5): Show | 8 | HG00735.hp2 HG00738.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-3761C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777155 | ||||||
chr1:9777217
|
C | CA | 88 | a0001c0001t0001g0136a0001c0001t0001g0174a0001c0003t0004g0261others(85): Show | 88 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(85): Show |
intron_variant | MODIFIER | c.92-3824dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777217 | ||||||
chr1:9777217
|
C | CAA | 13 | a0001c0001t0001g0238a0001c0006t0009g0266a0001c0006t0009g0267others(10): Show | 13 | HG00621.hp2 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-3825_92-3824dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777217 | ||||||
chr1:9777252
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.92-3858C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777252 | ||||||
chr1:9777345
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-3951A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777345 | ||||||
chr1:9777501
|
C | A | 3 | a0001c0003t0004g0115a0001c0003t0004g0116a0001c0003t0004g0119 | 3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-4107G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777501 | ||||||
chr1:9777526
|
AAAC | A | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-4135_92-4133del others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777526 | ||||||
chr1:9777759
|
T | G | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-4365A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777759 | ||||||
chr1:9777774
|
A | C | 269 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.92-4380T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777774 | ||||||
chr1:9777793
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.92-4399C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777793 | ||||||
chr1:9777823
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4429G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777823 | ||||||
chr1:9777942
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-4548G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777942 | ||||||
chr1:9777946
|
C | T | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-4552G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9777946 | ||||||
chr1:9778041
|
A | C | 1 | a0001c0008t0001g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.92-4647T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778041 | ||||||
chr1:9778223
|
A | AAC | 43 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.92-4831_92-4830dup others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACAC | 49 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0128others(46): Show | 49 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.92-4833_92-4830dup others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACACAC | 16 | a0001c0001t0001g0106a0001c0001t0001g0154a0001c0001t0001g0157others(13): Show | 16 | HG02258.hp2 HG02280.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.92-4835_92-4830dup others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0149a0001c0001t0001g0255a0001c0001t0004g0219others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-4837_92-4830dup others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.92-4839_92-4830dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACACACA others(13): Show |
1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-4849_92-4830dup others(20): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
A | AACACACA others(23): Show |
1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-4859_92-4830dup others(30): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
AAC | A | 32 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0152others(29): Show | 32 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-4831_92-4830del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
AACAC | A | 48 | a0001c0001t0001g0189a0001c0001t0001g0230a0001c0001t0001g0231others(45): Show | 48 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-4833_92-4830del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
AACACAC | A | 33 | a0001c0003t0006g0035a0001c0003t0006g0055a0001c0003t0006g0056others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.92-4835_92-4830del others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
AACACACA others(1): Show |
A | 3 | a0001c0003t0004g0109a0001c0003t0004g0120a0001c0003t0004g0121 | 3 | HG02622.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-4837_92-4830del others(8): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778223
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0001g0262a0001c0003t0004g0110 | 2 | HG00639.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.92-4839_92-4830del others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778223 | ||||||
chr1:9778382
|
G | A | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-4988C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778382 | ||||||
chr1:9778423
|
G | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0257 | 2 | HG01099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.92-5029C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778423 | ||||||
chr1:9778727
|
A | G | 2 | a0001c0003t0004g0120a0001c0003t0004g0121 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-5333T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778727 | ||||||
chr1:9778733
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-5339C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778733 | ||||||
chr1:9778742
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5348G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778742 | ||||||
chr1:9778743
|
G | A | 3 | a0001c0003t0004g0115a0001c0003t0004g0116a0001c0003t0004g0119 | 3 | HG02615.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.92-5349C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778743 | ||||||
chr1:9778897
|
A | T | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-5503T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9778897 | ||||||
chr1:9779023
|
C | CA | 49 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(46): Show | 49 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.92-5630dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779023 | ||||||
chr1:9779023
|
CA | C | 8 | a0001c0003t0007g0095a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG03139.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5630delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779023 | ||||||
chr1:9779072
|
G | A | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-5678C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779072 | ||||||
chr1:9779193
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-5799A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779193 | ||||||
chr1:9779260
|
T | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-5866A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779260 | ||||||
chr1:9779271
|
T | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-5877A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779271 | ||||||
chr1:9779294
|
C | T | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-5900G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779294 | ||||||
chr1:9779415
|
A | T | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-6021T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779415 | ||||||
chr1:9779810
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.92-6416T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779810 | ||||||
chr1:9779812
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.92-6418T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779812 | ||||||
chr1:9779855
|
C | CTTTTT | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-6466_92-6462dup others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9779855 | ||||||
chr1:9780064
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0224 | 2 | HG00738.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.92-6670T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780064 | ||||||
chr1:9780080
|
T | C | 124 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(121): Show | 124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-6686A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780080 | ||||||
chr1:9780150
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-6756G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780150 | ||||||
chr1:9780161
|
C | A | 5 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0001g0195others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6767G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780161 | ||||||
chr1:9780202
|
A | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-6808T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780202 | ||||||
chr1:9780225
|
AT | A | 94 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(91): Show | 94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.92-6832delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780225 | ||||||
chr1:9780311
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92-6917T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780311 | ||||||
chr1:9780420
|
C | T | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-7026G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780420 | ||||||
chr1:9780590
|
C | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7196G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780590 | ||||||
chr1:9780618
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.92-7224T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780618 | ||||||
chr1:9780661
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7267A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780661 | ||||||
chr1:9780680
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-7286C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780680 | ||||||
chr1:9780705
|
A | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-7311T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780705 | ||||||
chr1:9780771
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92-7377G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780771 | ||||||
chr1:9780828
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-7434G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780828 | ||||||
chr1:9780863
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-7469A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9780863 | ||||||
chr1:9781021
|
T | C | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-7627A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781021 | ||||||
chr1:9781060
|
G | T | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-7666C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781060 | ||||||
chr1:9781629
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.92-8235C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781629 | ||||||
chr1:9781680
|
T | C | 5 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-8286A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781680 | ||||||
chr1:9781814
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-8420G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781814 | ||||||
chr1:9781958
|
A | C | 1 | a0001c0003t0004g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.92-8564T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9781958 | ||||||
chr1:9782271
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-8877C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782271 | ||||||
chr1:9782403
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.92-9009G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782403 | ||||||
chr1:9782518
|
C | T | 204 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126others(201): Show | 204 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.92-9124G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782518 | ||||||
chr1:9782790
|
T | C | 6 | a0002c0002t0002g0007a0002c0002t0002g0024a0002c0002t0002g0025others(3): Show | 6 | HG02717.hp2 HG03130.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-9396A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782790 | ||||||
chr1:9782908
|
G | T | 94 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(91): Show | 94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.92-9514C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782908 | ||||||
chr1:9782988
|
C | T | 1 | a0002c0002t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.92-9594G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9782988 | ||||||
chr1:9783128
|
G | A | 124 | a0001c0001t0001g0262a0001c0003t0004g0108a0001c0003t0004g0109others(121): Show | 124 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.92-9734C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783128 | ||||||
chr1:9783172
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.92-9778A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783172 | ||||||
chr1:9783179
|
G | A | 1 | a0006c0015t0014g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-9785C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783179 | ||||||
chr1:9783289
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-9895G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783289 | ||||||
chr1:9783420
|
A | C | 1 | a0011c0009t0002g0002 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-10026T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783420 | ||||||
chr1:9783539
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-10145C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783539 | ||||||
chr1:9783593
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-10199G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783593 | ||||||
chr1:9783730
|
C | T | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-10336G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9783730 | ||||||
chr1:9784172
|
C | CA | 51 | a0001c0001t0001g0129a0001c0001t0001g0143a0001c0001t0001g0150others(48): Show | 51 | HG00280.hp2 HG00733.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-10779dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784172 | ||||||
chr1:9784172
|
CAAA | C | 7 | a0003c0004t0002g0064a0003c0004t0002g0065a0003c0004t0002g0066others(4): Show | 7 | HG00558.hp1 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-10781_92-10779d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784172 | ||||||
chr1:9784204
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-10810C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784204 | ||||||
chr1:9784578
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-11184A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784578 | ||||||
chr1:9784610
|
G | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11216C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784610 | ||||||
chr1:9784675
|
A | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-11281T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784675 | ||||||
chr1:9784682
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11288T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784682 | ||||||
chr1:9784704
|
C | A | 5 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0164others(2): Show | 5 | HG01346.hp1 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-11310G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784704 | ||||||
chr1:9784983
|
C | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-11589G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784983 | ||||||
chr1:9784996
|
C | CT | 13 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0203others(10): Show | 13 | HG00140.hp1 HG01261.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-11603dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784996 | ||||||
chr1:9784996
|
CT | C | 27 | a0001c0001t0001g0125a0001c0001t0001g0136a0001c0001t0001g0188others(24): Show | 27 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-11603delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9784996 | ||||||
chr1:9785158
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11764G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785158 | ||||||
chr1:9785439
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-12045A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785439 | ||||||
chr1:9785566
|
G | T | 1 | a0003c0004t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.92-12172C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785566 | ||||||
chr1:9785591
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12197C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785591 | ||||||
chr1:9785633
|
A | G | 1 | a0002c0002t0002g0089 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.92-12239T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785633 | ||||||
chr1:9785795
|
CT | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0166a0001c0003t0005g0008others(8): Show | 11 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-12402delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785795 | ||||||
chr1:9785795
|
CTT | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12403_92-12402d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785795 | ||||||
chr1:9785889
|
A | C | 3 | a0002c0002t0002g0007a0002c0002t0002g0025a0002c0002t0002g0039 | 3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92-12495T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785889 | ||||||
chr1:9785903
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-12509G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785903 | ||||||
chr1:9785940
|
T | C | 1 | a0002c0002t0002g0092 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.92-12546A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785940 | ||||||
chr1:9785970
|
G | A | 1 | a0002c0002t0002g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92-12576C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9785970 | ||||||
chr1:9786103
|
C | T | 2 | a0001c0003t0004g0120a0001c0003t0004g0121 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-12709G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786103 | ||||||
chr1:9786209
|
A | G | 86 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(83): Show | 86 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(83): Show |
intron_variant | MODIFIER | c.92-12815T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786209 | ||||||
chr1:9786283
|
T | C | 74 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(71): Show | 74 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.92-12889A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786283 | ||||||
chr1:9786433
|
G | A | 9 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-13039C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786433 | ||||||
chr1:9786563
|
G | A | 122 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(119): Show | 122 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(119): Show |
intron_variant | MODIFIER | c.92-13169C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786563 | ||||||
chr1:9786575
|
G | A | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-13181C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786575 | ||||||
chr1:9786592
|
GAGATTGT others(10034): Show |
G | 25 | a0001c0003t0006g0096a0002c0002t0002g0071a0002c0002t0002g0072others(22): Show | 25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-23239_92-13199d others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786592 | ||||||
chr1:9786644
|
G | A | 2 | a0004c0005t0001g0211a0004c0005t0001g0212 | 2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.92-13250C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786644 | ||||||
chr1:9786648
|
C | CA | 52 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0125others(49): Show | 52 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.92-13255dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | ||||||
chr1:9786648
|
C | CAA | 38 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0001t0001g0188others(35): Show | 38 | HG01081.hp1 HG01255.hp1 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.92-13256_92-13255d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | ||||||
chr1:9786648
|
C | CAAA | 32 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(29): Show | 32 | HG01123.hp2 HG01261.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.92-13257_92-13255d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | ||||||
chr1:9786648
|
CAAAA | C | 6 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0067others(3): Show | 6 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-13258_92-13255d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786648 | ||||||
chr1:9786665
|
A | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0203a0001c0001t0001g0216others(2): Show | 5 | HG02135.hp2 HG02155.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-13271T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786665 | ||||||
chr1:9786666
|
A | C | 1 | a0001c0001t0001g0264 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.92-13272T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786666 | ||||||
chr1:9786819
|
C | T | 1 | a0001c0003t0004g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-13425G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9786819 | ||||||
chr1:9787178
|
CAGA | C | 69 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(66): Show | 69 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(66): Show |
intron_variant | MODIFIER | c.92-13787_92-13785d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787178 | ||||||
chr1:9787189
|
GCTTCTGT others(6): Show |
G | 1 | a0002c0002t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.92-13808_92-13796d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787189 | ||||||
chr1:9787232
|
G | A | 5 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(2): Show | 5 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-13838C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787232 | ||||||
chr1:9787263
|
A | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0200a0001c0001t0001g0204others(3): Show | 6 | HG00609.hp1 HG02027.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-13869T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787263 | ||||||
chr1:9787402
|
A | AT | 26 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0157others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.92-14009dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787402 | ||||||
chr1:9787402
|
A | ATTTTT | 5 | a0003c0004t0002g0063a0003c0004t0002g0066a0003c0004t0002g0067others(2): Show | 5 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-14013_92-14009d others(7): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787402 | ||||||
chr1:9787427
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14033C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787427 | ||||||
chr1:9787442
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14048G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787442 | ||||||
chr1:9787496
|
C | T | 1 | a0001c0003t0004g0111 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.92-14102G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787496 | ||||||
chr1:9787529
|
G | A | 2 | a0002c0002t0003g0022a0002c0002t0003g0029 | 2 | HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.92-14135C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787529 | ||||||
chr1:9787558
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-14164G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787558 | ||||||
chr1:9787594
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.92-14200C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787594 | ||||||
chr1:9787704
|
C | T | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-14310G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787704 | ||||||
chr1:9787715
|
C | G | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-14321G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787715 | ||||||
chr1:9787913
|
C | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-14519G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9787913 | ||||||
chr1:9788024
|
G | A | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-14630C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788024 | ||||||
chr1:9788063
|
C | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.92-14669G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788063 | ||||||
chr1:9788075
|
C | T | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-14681G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788075 | ||||||
chr1:9788088
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.92-14694G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788088 | ||||||
chr1:9788291
|
C | T | 1 | a0001c0003t0004g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-14897G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788291 | ||||||
chr1:9788302
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-14908T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788302 | ||||||
chr1:9788442
|
A | G | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-15048T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788442 | ||||||
chr1:9788445
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15051G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788445 | ||||||
chr1:9788541
|
C | T | 1 | a0001c0003t0004g0111 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.92-15147G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788541 | ||||||
chr1:9788566
|
CA | C | 9 | a0001c0001t0001g0203a0003c0004t0002g0063a0003c0004t0002g0064others(6): Show | 9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-15173delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788566 | ||||||
chr1:9788734
|
G | A | 2 | a0001c0003t0004g0111a0001c0003t0004g0112 | 2 | HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-15340C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788734 | ||||||
chr1:9788855
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-15461C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788855 | ||||||
chr1:9788867
|
CA | C | 206 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.92-15474delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788867 | ||||||
chr1:9788867
|
CAAA | C | 7 | a0003c0004t0002g0063a0003c0004t0002g0065a0003c0004t0002g0066others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-15476_92-15474d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788867 | ||||||
chr1:9788875
|
A | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15481T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788875 | ||||||
chr1:9788879
|
A | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-15485T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788879 | ||||||
chr1:9788885
|
A | C | 1 | a0001c0003t0004g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-15491T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9788885 | ||||||
chr1:9789014
|
C | CCTTT | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-15624_92-15621d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789014 | ||||||
chr1:9789148
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.92-15754G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789148 | ||||||
chr1:9789193
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-15799C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789193 | ||||||
chr1:9789300
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-15906G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789300 | ||||||
chr1:9789346
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-15952A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789346 | ||||||
chr1:9789364
|
T | C | 1 | a0001c0003t0005g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92-15970A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789364 | ||||||
chr1:9789586
|
A | G | 2 | a0002c0002t0003g0050a0002c0002t0003g0051 | 2 | NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.92-16192T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789586 | ||||||
chr1:9789796
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92-16402A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789796 | ||||||
chr1:9789894
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-16500C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789894 | ||||||
chr1:9789954
|
G | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-16560C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9789954 | ||||||
chr1:9790009
|
C | T | 1 | a0002c0002t0002g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-16615G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790009 | ||||||
chr1:9790155
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0202 | 3 | HG01255.hp2 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.92-16761T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790155 | ||||||
chr1:9790171
|
T | C | 2 | a0002c0002t0002g0014a0002c0002t0002g0016 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92-16777A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790171 | ||||||
chr1:9790189
|
A | G | 2 | a0002c0002t0003g0021a0002c0002t0003g0049 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.92-16795T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790189 | ||||||
chr1:9790354
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-16960A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790354 | ||||||
chr1:9790437
|
C | A | 1 | a0001c0016t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.92-17043G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790437 | ||||||
chr1:9790440
|
T | G | 5 | a0002c0002t0003g0023a0002c0002t0003g0032a0002c0002t0003g0033others(2): Show | 5 | HG02698.hp1 NA18943.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17046A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790440 | ||||||
chr1:9790451
|
AAC | A | 61 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(58): Show | 61 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.92-17059_92-17058d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790451 | ||||||
chr1:9790483
|
C | T | 1 | a0002c0002t0002g0047 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.92-17089G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790483 | ||||||
chr1:9790521
|
T | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-17127A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790521 | ||||||
chr1:9790565
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.92-17171T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790565 | ||||||
chr1:9790617
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-17223T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790617 | ||||||
chr1:9790769
|
G | A | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-17375C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790769 | ||||||
chr1:9790855
|
C | T | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-17461G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790855 | ||||||
chr1:9790865
|
G | A | 61 | a0001c0003t0006g0035a0001c0003t0006g0046a0001c0003t0006g0055others(58): Show | 61 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.92-17471C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790865 | ||||||
chr1:9790915
|
T | C | 98 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(95): Show | 98 | HG00558.hp1 HG00733.hp2 HG01081.hp1 others(95): Show |
intron_variant | MODIFIER | c.92-17521A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790915 | ||||||
chr1:9790916
|
G | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-17522C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790916 | ||||||
chr1:9790930
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.92-17536C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790930 | ||||||
chr1:9790960
|
C | T | 1 | a0002c0002t0003g0023 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.92-17566G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9790960 | ||||||
chr1:9791064
|
G | A | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-17670C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791064 | ||||||
chr1:9791096
|
C | T | 1 | a0001c0001t0018g0173 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.92-17702G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791096 | ||||||
chr1:9791141
|
C | CA | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0131others(3): Show | 6 | HG01243.hp2 HG02027.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-17748dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | ||||||
chr1:9791141
|
CA | C | 77 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0004g0183others(74): Show | 77 | HG00558.hp2 HG00733.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.92-17748delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | ||||||
chr1:9791141
|
CAA | C | 13 | a0001c0001t0001g0262a0001c0003t0004g0120a0001c0003t0004g0122others(10): Show | 13 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-17749_92-17748d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791141 | ||||||
chr1:9791170
|
T | TTAA | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-17777_92-17776i others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791170 | ||||||
chr1:9791209
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-17815A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791209 | ||||||
chr1:9791382
|
C | A | 1 | a0002c0002t0002g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-17988G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791382 | ||||||
chr1:9791532
|
C | T | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-18138G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791532 | ||||||
chr1:9791619
|
C | T | 2 | a0002c0002t0002g0014a0002c0002t0002g0016 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92-18225G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791619 | ||||||
chr1:9791656
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18262A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791656 | ||||||
chr1:9791660
|
A | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18266T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791660 | ||||||
chr1:9791663
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18269A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791663 | ||||||
chr1:9791676
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18282A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791676 | ||||||
chr1:9791677
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-18283C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791677 | ||||||
chr1:9791755
|
A | C | 1 | a0009c0012t0003g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92-18361T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791755 | ||||||
chr1:9791829
|
C | T | 1 | a0001c0003t0005g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92-18435G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791829 | ||||||
chr1:9791848
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0188others(3): Show | 6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-18454C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9791848 | ||||||
chr1:9792033
|
C | T | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-18639G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792033 | ||||||
chr1:9792084
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.92-18690C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792084 | ||||||
chr1:9792141
|
G | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-18747C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792141 | ||||||
chr1:9792164
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.92-18770G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792164 | ||||||
chr1:9792171
|
G | A | 1 | a0001c0003t0005g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-18777C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792171 | ||||||
chr1:9792185
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18791T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792185 | ||||||
chr1:9792213
|
C | A | 34 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0001g0154others(31): Show | 34 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.92-18819G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792213 | ||||||
chr1:9792216
|
A | C | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-18822T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792216 | ||||||
chr1:9792263
|
A | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-18869T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792263 | ||||||
chr1:9792272
|
G | A | 1 | a0002c0002t0002g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92-18878C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792272 | ||||||
chr1:9792306
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18912T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792306 | ||||||
chr1:9792339
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-18945A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792339 | ||||||
chr1:9792434
|
C | G | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-19040G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792434 | ||||||
chr1:9792705
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-19311T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792705 | ||||||
chr1:9792770
|
C | G | 2 | a0001c0003t0007g0037a0001c0003t0007g0095 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.92-19376G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792770 | ||||||
chr1:9792794
|
G | T | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-19400C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9792794 | ||||||
chr1:9793461
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-20067C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9793461 | ||||||
chr1:9793494
|
G | A | 3 | a0002c0002t0002g0019a0002c0002t0002g0020a0011c0009t0002g0002 | 3 | HG01891.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.92-20100C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9793494 | ||||||
chr1:9794058
|
G | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-20664C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794058 | ||||||
chr1:9794068
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.92-20674A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794068 | ||||||
chr1:9794143
|
G | A | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-20749C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794143 | ||||||
chr1:9794180
|
A | G | 225 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.92-20786T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794180 | ||||||
chr1:9794212
|
C | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.92-20818G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794212 | ||||||
chr1:9794427
|
A | G | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-21033T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794427 | ||||||
chr1:9794714
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-21320A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794714 | ||||||
chr1:9794715
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-21321C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794715 | ||||||
chr1:9794734
|
C | A | 15 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(12): Show | 15 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.92-21340G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794734 | ||||||
chr1:9794837
|
T | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92-21443A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794837 | ||||||
chr1:9794918
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92-21524C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9794918 | ||||||
chr1:9795021
|
GA | G | 87 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(84): Show | 87 | HG00733.hp2 HG01081.hp1 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.92-21628delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795021 | ||||||
chr1:9795025
|
A | G | 6 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0188others(3): Show | 6 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-21631T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795025 | ||||||
chr1:9795032
|
A | G | 1 | a0003c0004t0002g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.92-21638T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795032 | ||||||
chr1:9795033
|
A | G | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-21639T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795033 | ||||||
chr1:9795034
|
G | A | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-21640C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795034 | ||||||
chr1:9795167
|
CT | C | 14 | a0001c0006t0009g0266a0001c0006t0009g0267a0002c0002t0002g0010others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-21774delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795167 | ||||||
chr1:9795205
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-21811C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795205 | ||||||
chr1:9795326
|
C | T | 1 | a0001c0003t0004g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92-21932G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795326 | ||||||
chr1:9795354
|
C | T | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-21960G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795354 | ||||||
chr1:9795413
|
G | A | 1 | a0001c0008t0001g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.92-22019C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795413 | ||||||
chr1:9795441
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-22047A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795441 | ||||||
chr1:9795471
|
C | T | 244 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.92-22077G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795471 | ||||||
chr1:9795503
|
G | T | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.92-22109C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795503 | ||||||
chr1:9795632
|
T | G | 2 | a0002c0002t0003g0048a0002c0002t0003g0054 | 2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.92-22238A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795632 | ||||||
chr1:9795957
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.92-22563G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795957 | ||||||
chr1:9795961
|
CA | C | 175 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0126others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.92-22568delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9795961 | ||||||
chr1:9796122
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-22728G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796122 | ||||||
chr1:9796154
|
C | T | 1 | a0001c0001t0008g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-22760G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796154 | ||||||
chr1:9796225
|
G | A | 6 | a0001c0001t0001g0210a0001c0003t0005g0008a0001c0003t0005g0009others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-22831C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796225 | ||||||
chr1:9796240
|
C | T | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.92-22846G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796240 | ||||||
chr1:9796260
|
CAAAAACA others(5): Show |
C | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.92-22878_92-22867d others(14): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796260 | ||||||
chr1:9796262
|
A | G | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-22868T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796262 | ||||||
chr1:9796266
|
CA | C | 161 | a0001c0001t0001g0105a0001c0001t0001g0125a0001c0001t0001g0126others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.92-22873delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796266 | ||||||
chr1:9796266
|
CAA | C | 15 | a0001c0001t0001g0147a0001c0003t0005g0097a0001c0003t0005g0098others(12): Show | 15 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-22874_92-22873d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796266 | ||||||
chr1:9796272
|
AAAAAACA others(6): Show |
A | 4 | a0001c0003t0004g0111a0001c0003t0004g0112a0001c0003t0007g0037others(1): Show | 4 | HG02897.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-22891_92-22879d others(15): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796272 | ||||||
chr1:9796298
|
A | C | 3 | a0001c0003t0004g0111a0001c0003t0004g0112a0001c0003t0007g0037 | 3 | HG02897.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-22904T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796298 | ||||||
chr1:9796300
|
A | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0262 | 2 | HG00639.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.92-22906T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796300 | ||||||
chr1:9796403
|
G | A | 3 | a0001c0003t0004g0261a0001c0006t0009g0266a0001c0006t0009g0267 | 3 | HG01109.hp1 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-23009C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796403 | ||||||
chr1:9796414
|
C | T | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-23020G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796414 | ||||||
chr1:9796447
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.92-23053G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796447 | ||||||
chr1:9796556
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-23162G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796556 | ||||||
chr1:9796557
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.92-23163C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796557 | ||||||
chr1:9796569
|
A | G | 9 | a0001c0001t0001g0167a0003c0004t0002g0063a0003c0004t0002g0064others(6): Show | 9 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-23175T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796569 | ||||||
chr1:9796577
|
A | G | 183 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.92-23183T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796577 | ||||||
chr1:9796641
|
G | A | 25 | a0001c0003t0006g0096a0002c0002t0002g0071a0002c0002t0002g0072others(22): Show | 25 | HG00423.hp2 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.92-23247C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796641 | ||||||
chr1:9796657
|
C | T | 5 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(2): Show | 5 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-23263G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796657 | ||||||
chr1:9796768
|
T | G | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-23374A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796768 | ||||||
chr1:9796804
|
G | C | 2 | a0002c0002t0003g0044a0002c0002t0003g0045 | 2 | NA18943.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.92-23410C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796804 | ||||||
chr1:9796933
|
C | T | 1 | a0002c0002t0002g0071 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.92-23539G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796933 | ||||||
chr1:9796934
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92-23540C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796934 | ||||||
chr1:9796993
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.92-23599G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9796993 | ||||||
chr1:9797072
|
A | G | 2 | a0001c0003t0004g0120a0001c0003t0004g0121 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.92-23678T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797072 | ||||||
chr1:9797268
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-23874C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797268 | ||||||
chr1:9797320
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-23926C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797320 | ||||||
chr1:9797581
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.92-24187G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797581 | ||||||
chr1:9797684
|
A | C | 1 | a0009c0012t0003g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92-24290T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797684 | ||||||
chr1:9797716
|
G | C | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-24322C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797716 | ||||||
chr1:9797722
|
T | G | 2 | a0004c0005t0001g0211a0004c0005t0001g0212 | 2 | HG01258.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.92-24328A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797722 | ||||||
chr1:9797744
|
T | C | 1 | a0002c0002t0002g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92-24350A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797744 | ||||||
chr1:9797954
|
C | T | 2 | a0001c0003t0005g0097a0001c0003t0005g0098 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.92-24560G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9797954 | ||||||
chr1:9798085
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0198a0001c0001t0001g0213 | 3 | NA18942.hp1 NA18943.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.92-24691C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798085 | ||||||
chr1:9798105
|
AGAGAGAG others(1): Show |
A | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-24719_92-24712d others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798105 | ||||||
chr1:9798124
|
G | GAGAGGGG others(9): Show |
1 | a0002c0002t0002g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.92-24746_92-24731d others(18): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798124 | ||||||
chr1:9798274
|
C | T | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-24880G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798274 | ||||||
chr1:9798356
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.92-24962C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798356 | ||||||
chr1:9798742
|
C | A | 1 | a0002c0002t0003g0044 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.91+24901G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798742 | ||||||
chr1:9798799
|
G | A | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+24844C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798799 | ||||||
chr1:9798845
|
C | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+24798G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9798845 | ||||||
chr1:9799030
|
A | G | 1 | a0002c0002t0003g0029 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.91+24613T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799030 | ||||||
chr1:9799280
|
C | T | 1 | a0001c0003t0005g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91+24363G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799280 | ||||||
chr1:9799327
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+24316A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799327 | ||||||
chr1:9799370
|
G | C | 1 | a0001c0003t0005g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+24273C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799370 | ||||||
chr1:9799670
|
C | T | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+23973G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799670 | ||||||
chr1:9799681
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+23962C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799681 | ||||||
chr1:9799766
|
A | C | 99 | a0001c0001t0001g0106a0001c0003t0004g0108a0001c0003t0004g0109others(96): Show | 99 | HG00558.hp1 HG00733.hp2 HG01081.hp1 others(96): Show |
intron_variant | MODIFIER | c.91+23877T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799766 | ||||||
chr1:9799802
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02922.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.91+23841C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799802 | ||||||
chr1:9799820
|
A | C | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+23823T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799820 | ||||||
chr1:9799962
|
A | T | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+23681T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799962 | ||||||
chr1:9799982
|
C | G | 2 | a0002c0002t0002g0071a0002c0002t0002g0081 | 2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.91+23661G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799982 | ||||||
chr1:9799992
|
C | A | 196 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.91+23651G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9799992 | ||||||
chr1:9800120
|
GA | G | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+23522delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800120 | ||||||
chr1:9800462
|
G | A | 1 | a0002c0002t0002g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+23181C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800462 | ||||||
chr1:9800504
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+23139C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800504 | ||||||
chr1:9800557
|
G | GAAA | 6 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(3): Show | 6 | HG01981.hp2 NA18940.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+23083_91+23085d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800557 | ||||||
chr1:9800557
|
GA | G | 120 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.91+23085delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800557 | ||||||
chr1:9800607
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+23036C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800607 | ||||||
chr1:9800627
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91+23016C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800627 | ||||||
chr1:9800645
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22998T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800645 | ||||||
chr1:9800662
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+22981C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800662 | ||||||
chr1:9800729
|
CA | C | 83 | a0001c0001t0001g0106a0001c0001t0001g0255a0001c0001t0001g0256others(80): Show | 83 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.91+22913delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800729 | ||||||
chr1:9800740
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.91+22903A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800740 | ||||||
chr1:9800767
|
G | GA | 9 | a0001c0003t0004g0122a0003c0004t0002g0063a0003c0004t0002g0064others(6): Show | 9 | HG00558.hp1 HG01981.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+22875dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800767 | ||||||
chr1:9800841
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+22802T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800841 | ||||||
chr1:9800886
|
C | T | 51 | a0001c0001t0001g0106a0001c0003t0006g0035a0001c0003t0006g0046others(48): Show | 51 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+22757G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800886 | ||||||
chr1:9800909
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+22734T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800909 | ||||||
chr1:9800940
|
A | AAAAG | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22702_91+22703i others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800940 | ||||||
chr1:9800974
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+22669G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800974 | ||||||
chr1:9800979
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.91+22664C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9800979 | ||||||
chr1:9801079
|
T | C | 74 | a0001c0001t0001g0106a0001c0001t0001g0255a0001c0001t0001g0256others(71): Show | 74 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(71): Show |
intron_variant | MODIFIER | c.91+22564A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801079 | ||||||
chr1:9801231
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22412C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801231 | ||||||
chr1:9801313
|
TTA | T | 6 | a0002c0002t0002g0043a0002c0002t0002g0047a0002c0002t0002g0059others(3): Show | 6 | NA18948.hp2 NA18984.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+22328_91+22329d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801313 | ||||||
chr1:9801321
|
T | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+22322A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801321 | ||||||
chr1:9801548
|
CATT | C | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+22092_91+22094d others(5): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801548 | ||||||
chr1:9801578
|
G | C | 9 | a0002c0002t0002g0074a0002c0002t0002g0075a0002c0002t0002g0079others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+22065C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801578 | ||||||
chr1:9801716
|
G | A | 3 | a0002c0002t0002g0007a0002c0002t0002g0025a0002c0002t0002g0039 | 3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.91+21927C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801716 | ||||||
chr1:9801986
|
T | C | 1 | a0002c0010t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91+21657A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9801986 | ||||||
chr1:9802010
|
T | C | 1 | a0001c0003t0005g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.91+21633A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802010 | ||||||
chr1:9802314
|
C | T | 166 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.91+21329G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802314 | ||||||
chr1:9802423
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.91+21220A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802423 | ||||||
chr1:9802424
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+21219C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802424 | ||||||
chr1:9802536
|
A | C | 1 | a0002c0002t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.91+21107T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802536 | ||||||
chr1:9802702
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0226 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.91+20941G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802702 | ||||||
chr1:9802710
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20933C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802710 | ||||||
chr1:9802713
|
AC | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02135.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+20929delG | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802713 | ||||||
chr1:9802804
|
A | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+20839T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802804 | ||||||
chr1:9802823
|
A | AT | 160 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.91+20819dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | ||||||
chr1:9802823
|
A | ATT | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0142others(12): Show | 15 | HG00733.hp1 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+20818_91+20819d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | ||||||
chr1:9802823
|
AT | A | 10 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(7): Show | 10 | HG00558.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+20819delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9802823 | ||||||
chr1:9803072
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+20571G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803072 | ||||||
chr1:9803158
|
C | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0015g0237 | 3 | HG00621.hp2 HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.91+20485G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803158 | ||||||
chr1:9803263
|
A | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20380T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803263 | ||||||
chr1:9803402
|
C | T | 2 | a0002c0002t0003g0044a0002c0002t0003g0045 | 2 | NA18943.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.91+20241G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803402 | ||||||
chr1:9803470
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+20173G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803470 | ||||||
chr1:9803524
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+20119G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803524 | ||||||
chr1:9803631
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.91+20012G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803631 | ||||||
chr1:9803632
|
G | A | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+20011C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803632 | ||||||
chr1:9803792
|
A | G | 7 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+19851T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803792 | ||||||
chr1:9803825
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.91+19818A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803825 | ||||||
chr1:9803832
|
T | A | 6 | a0001c0003t0004g0115a0001c0003t0004g0116a0001c0003t0004g0117others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+19811A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803832 | ||||||
chr1:9803976
|
A | G | 3 | a0001c0001t0001g0181a0001c0001t0008g0141a0001c0001t0008g0240 | 3 | HG02647.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.91+19667T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9803976 | ||||||
chr1:9804055
|
T | C | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+19588A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804055 | ||||||
chr1:9804088
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+19555A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804088 | ||||||
chr1:9804147
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+19496C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804147 | ||||||
chr1:9804220
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+19423C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804220 | ||||||
chr1:9804256
|
A | G | 1 | a0003c0004t0002g0068 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.91+19387T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804256 | ||||||
chr1:9804323
|
A | C | 1 | a0002c0002t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.91+19320T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804323 | ||||||
chr1:9804340
|
C | T | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+19303G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804340 | ||||||
chr1:9804361
|
C | CA | 21 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(18): Show | 21 | HG00558.hp1 HG01261.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.91+19281dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | ||||||
chr1:9804361
|
CA | C | 105 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0192others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.91+19281delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | ||||||
chr1:9804361
|
CAA | C | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.91+19280_91+19281d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804361 | ||||||
chr1:9804394
|
A | G | 76 | a0001c0001t0001g0106a0001c0003t0006g0035a0001c0003t0006g0046others(73): Show | 76 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.91+19249T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804394 | ||||||
chr1:9804407
|
G | A | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+19236C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804407 | ||||||
chr1:9804435
|
C | T | 94 | a0001c0001t0001g0106a0001c0003t0005g0008a0001c0003t0005g0009others(91): Show | 94 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.91+19208G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804435 | ||||||
chr1:9804769
|
C | T | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.91+18874G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804769 | ||||||
chr1:9804867
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.91+18776C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9804867 | ||||||
chr1:9805058
|
T | C | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+18585A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805058 | ||||||
chr1:9805206
|
C | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+18437G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805206 | ||||||
chr1:9805556
|
G | A | 1 | a0002c0002t0017g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+18087C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805556 | ||||||
chr1:9805575
|
G | A | 172 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.91+18068C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805575 | ||||||
chr1:9805591
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.91+18052C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805591 | ||||||
chr1:9805633
|
G | A | 1 | a0002c0002t0002g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.91+18010C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805633 | ||||||
chr1:9805740
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+17903C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805740 | ||||||
chr1:9805745
|
T | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+17898A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805745 | ||||||
chr1:9805866
|
C | CA | 97 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0136others(94): Show | 97 | HG00423.hp2 HG00738.hp1 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.91+17776dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | ||||||
chr1:9805866
|
C | CAA | 7 | a0001c0003t0005g0008a0002c0002t0002g0025a0002c0002t0002g0078others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+17775_91+17776d others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | ||||||
chr1:9805866
|
CA | C | 13 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0197others(10): Show | 13 | HG00558.hp1 HG01070.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.91+17776delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9805866 | ||||||
chr1:9806205
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.91+17438C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806205 | ||||||
chr1:9806223
|
G | A | 162 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.91+17420C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806223 | ||||||
chr1:9806379
|
G | T | 46 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(43): Show | 46 | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+17264C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806379 | ||||||
chr1:9806600
|
C | T | 9 | a0002c0002t0002g0074a0002c0002t0002g0075a0002c0002t0002g0079others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+17043G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806600 | ||||||
chr1:9806662
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+16981C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806662 | ||||||
chr1:9806704
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+16939G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806704 | ||||||
chr1:9806740
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02135.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+16903C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806740 | ||||||
chr1:9806898
|
C | T | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+16745G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806898 | ||||||
chr1:9806917
|
C | T | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+16726G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9806917 | ||||||
chr1:9807009
|
C | T | 2 | a0002c0002t0003g0022a0002c0002t0003g0029 | 2 | HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.91+16634G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807009 | ||||||
chr1:9807012
|
G | C | 3 | a0002c0002t0002g0007a0002c0002t0002g0025a0002c0002t0002g0039 | 3 | HG03831.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.91+16631C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807012 | ||||||
chr1:9807227
|
C | G | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+16416G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807227 | ||||||
chr1:9807341
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+16302G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807341 | ||||||
chr1:9807367
|
C | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+16276G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807367 | ||||||
chr1:9807368
|
G | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+16275C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807368 | ||||||
chr1:9807893
|
C | T | 1 | a0002c0002t0002g0004 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.91+15750G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9807893 | ||||||
chr1:9808002
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+15641G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808002 | ||||||
chr1:9808005
|
C | T | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+15638G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808005 | ||||||
chr1:9808036
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02027.hp1 HG02523.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.91+15607G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808036 | ||||||
chr1:9808047
|
G | A | 3 | a0002c0002t0002g0019a0002c0002t0002g0020a0011c0009t0002g0002 | 3 | HG01891.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.91+15596C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808047 | ||||||
chr1:9808054
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91+15589G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808054 | ||||||
chr1:9808330
|
G | A | 3 | a0001c0003t0006g0035a0001c0003t0006g0055a0001c0003t0006g0056 | 3 | HG01255.hp1 HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.91+15313C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808330 | ||||||
chr1:9808529
|
A | G | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+15114T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808529 | ||||||
chr1:9808601
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.91+15042G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808601 | ||||||
chr1:9808602
|
G | T | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+15041C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808602 | ||||||
chr1:9808638
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.91+15005C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808638 | ||||||
chr1:9808692
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14951C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808692 | ||||||
chr1:9808698
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14945C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808698 | ||||||
chr1:9808743
|
C | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+14900G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808743 | ||||||
chr1:9808748
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+14895T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9808748 | ||||||
chr1:9809182
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91+14461A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809182 | ||||||
chr1:9809188
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+14455G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809188 | ||||||
chr1:9809272
|
C | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+14371G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809272 | ||||||
chr1:9809289
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91+14354T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809289 | ||||||
chr1:9809808
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+13835C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809808 | ||||||
chr1:9809863
|
C | T | 197 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.91+13780G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809863 | ||||||
chr1:9809984
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.91+13659T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9809984 | ||||||
chr1:9810071
|
A | G | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+13572T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810071 | ||||||
chr1:9810091
|
A | AGGAG | 9 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+13548_91+13551d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810091 | ||||||
chr1:9810141
|
A | AAGGGAAG others(136): Show |
1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(145): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(111): Show |
2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(120): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(153): Show |
8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(162): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(134): Show |
1 | a0001c0001t0001g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(133): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0220 | 2 | HG02145.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(134): Show |
1 | a0002c0002t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(133): Show |
3 | a0001c0003t0005g0009a0002c0002t0002g0043a0002c0002t0002g0078 | 3 | HG03209.hp1 NA18979.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(132): Show |
1 | a0002c0002t0002g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(141): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(132): Show |
2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(141): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(133): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0257a0002c0002t0002g0072others(1): Show | 4 | HG00423.hp2 HG01099.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(132): Show |
208 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0126others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(141): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(153): Show |
2 | a0001c0001t0001g0246a0002c0002t0002g0073 | 2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(162): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(195): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0001g0195others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(204): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(131): Show |
1 | a0002c0002t0003g0021 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(140): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(111): Show |
1 | a0002c0002t0002g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(120): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(127): Show |
1 | a0001c0003t0004g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+13501_91+13502i others(136): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(131): Show |
15 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(12): Show | 15 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(140): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(105): Show |
2 | a0001c0001t0004g0183a0001c0001t0004g0219 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(114): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(156): Show |
1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(165): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(134): Show |
1 | a0001c0001t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(134): Show |
2 | a0001c0001t0001g0125a0002c0002t0003g0042 | 2 | HG02027.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.91+13501_91+13502i others(143): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810141
|
A | AAGGGAAG others(133): Show |
5 | a0001c0001t0001g0166a0001c0001t0001g0193a0001c0001t0001g0236others(2): Show | 5 | HG00558.hp2 HG02523.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+13501_91+13502i others(142): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810141 | ||||||
chr1:9810230
|
C | T | 3 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099 | 3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.91+13413G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810230 | ||||||
chr1:9810272
|
ACGAGACC others(292): Show |
A | 1 | a0001c0003t0004g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.91+13072_91+13370d others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810272 | ||||||
chr1:9810731
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+12912G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810731 | ||||||
chr1:9810903
|
A | T | 70 | a0001c0001t0001g0106a0001c0003t0005g0008a0001c0003t0005g0009others(67): Show | 70 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(67): Show |
intron_variant | MODIFIER | c.91+12740T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810903 | ||||||
chr1:9810946
|
T | C | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12697A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810946 | ||||||
chr1:9810957
|
C | T | 70 | a0001c0001t0001g0106a0001c0003t0005g0008a0001c0003t0005g0009others(67): Show | 70 | HG01081.hp1 HG01123.hp2 HG01255.hp1 others(67): Show |
intron_variant | MODIFIER | c.91+12686G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9810957 | ||||||
chr1:9811167
|
G | A | 6 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0216others(3): Show | 6 | HG00140.hp1 HG02135.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12476C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811167 | ||||||
chr1:9811173
|
G | C | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12470C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811173 | ||||||
chr1:9811214
|
T | C | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12429A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811214 | ||||||
chr1:9811224
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+12419A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811224 | ||||||
chr1:9811225
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+12418G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811225 | ||||||
chr1:9811252
|
G | A | 1 | a0002c0002t0002g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+12391C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811252 | ||||||
chr1:9811542
|
TA | T | 6 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12100delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811542 | ||||||
chr1:9811731
|
C | CA | 30 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 30 | HG00609.hp1 HG00733.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.91+11911dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811731 | ||||||
chr1:9811731
|
CA | C | 50 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0218others(47): Show | 50 | HG00558.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.91+11911delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811731 | ||||||
chr1:9811747
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.91+11896T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811747 | ||||||
chr1:9811802
|
G | GT | 38 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0001g0149others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.91+11840dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9811802 | ||||||
chr1:9812143
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+11500T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812143 | ||||||
chr1:9812144
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+11499G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812144 | ||||||
chr1:9812260
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+11383C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812260 | ||||||
chr1:9812296
|
G | A | 3 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099 | 3 | HG02280.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.91+11347C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812296 | ||||||
chr1:9812314
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+11329A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812314 | ||||||
chr1:9812351
|
C | T | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+11292G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812351 | ||||||
chr1:9812455
|
G | C | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+11188C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812455 | ||||||
chr1:9812494
|
G | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+11149C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812494 | ||||||
chr1:9812613
|
G | A | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+11030C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812613 | ||||||
chr1:9812667
|
A | G | 1 | a0002c0002t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+10976T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812667 | ||||||
chr1:9812671
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+10972T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812671 | ||||||
chr1:9812713
|
T | C | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+10930A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812713 | ||||||
chr1:9812848
|
C | CA | 10 | a0001c0001t0001g0136a0001c0001t0001g0147a0001c0001t0001g0239others(7): Show | 10 | HG01081.hp1 HG01243.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+10794dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812848 | ||||||
chr1:9812848
|
C | CAAAA | 7 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10791_91+10794d others(6): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812848 | ||||||
chr1:9812866
|
C | A | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+10777G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812866 | ||||||
chr1:9812993
|
A | G | 268 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.91+10650T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9812993 | ||||||
chr1:9813004
|
A | T | 1 | a0002c0002t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+10639T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813004 | ||||||
chr1:9813114
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG00621.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10529C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813114 | ||||||
chr1:9813199
|
A | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+10444T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813199 | ||||||
chr1:9813362
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.91+10281C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813362 | ||||||
chr1:9813493
|
T | A | 106 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.91+10150A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813493 | ||||||
chr1:9813494
|
G | A | 105 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.91+10149C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813494 | ||||||
chr1:9813497
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10146A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813497 | ||||||
chr1:9813498
|
C | CA | 16 | a0001c0001t0001g0131a0001c0001t0001g0262a0001c0001t0008g0240others(13): Show | 16 | HG00558.hp1 HG00639.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+10144dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813498 | ||||||
chr1:9813498
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10145G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813498 | ||||||
chr1:9813499
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+10144T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813499 | ||||||
chr1:9813509
|
A | C | 1 | a0007c0017t0010g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+10134T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813509 | ||||||
chr1:9813836
|
G | A | 1 | a0001c0003t0004g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+9807C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813836 | ||||||
chr1:9813840
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+9803G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813840 | ||||||
chr1:9813881
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.91+9762G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813881 | ||||||
chr1:9813887
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+9756C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9813887 | ||||||
chr1:9814032
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.91+9611T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814032 | ||||||
chr1:9814074
|
C | G | 2 | a0002c0002t0002g0071a0002c0002t0002g0081 | 2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.91+9569G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814074 | ||||||
chr1:9814100
|
T | C | 17 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.91+9543A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814100 | ||||||
chr1:9814137
|
T | C | 1 | a0001c0003t0007g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+9506A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814137 | ||||||
chr1:9814240
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+9403A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814240 | ||||||
chr1:9814247
|
C | CA | 47 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(44): Show | 47 | HG00609.hp1 HG00621.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.91+9395dupT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | ||||||
chr1:9814247
|
C | CAAAAAAA others(3): Show |
6 | a0003c0004t0002g0063a0003c0004t0002g0066a0003c0004t0002g0067others(3): Show | 6 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+9386_91+9395dup others(10): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | ||||||
chr1:9814247
|
C | CAAAAAAA others(4): Show |
2 | a0003c0004t0002g0064a0003c0004t0002g0065 | 2 | NA18940.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.91+9385_91+9395dup others(11): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814247 | ||||||
chr1:9814345
|
C | T | 13 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(10): Show | 13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+9298G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814345 | ||||||
chr1:9814488
|
A | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+9155T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814488 | ||||||
chr1:9814620
|
G | A | 1 | a0002c0002t0003g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91+9023C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814620 | ||||||
chr1:9814744
|
T | C | 170 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.91+8899A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814744 | ||||||
chr1:9814774
|
C | T | 16 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(13): Show | 16 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.91+8869G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814774 | ||||||
chr1:9814812
|
T | C | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+8831A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814812 | ||||||
chr1:9814899
|
CA | C | 204 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.91+8743delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814899 | ||||||
chr1:9814918
|
A | T | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+8725T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9814918 | ||||||
chr1:9815034
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.91+8609C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815034 | ||||||
chr1:9815123
|
C | G | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+8520G>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815123 | ||||||
chr1:9815245
|
TA | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+8397delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815245 | ||||||
chr1:9815283
|
C | T | 206 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.91+8360G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815283 | ||||||
chr1:9815289
|
C | T | 206 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.91+8354G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815289 | ||||||
chr1:9815429
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+8214T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815429 | ||||||
chr1:9815430
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+8213A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815430 | ||||||
chr1:9815460
|
T | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+8183A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815460 | ||||||
chr1:9815510
|
A | G | 3 | a0002c0002t0002g0027a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02258.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.91+8133T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815510 | ||||||
chr1:9815575
|
C | T | 218 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.91+8068G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815575 | ||||||
chr1:9815697
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7946T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815697 | ||||||
chr1:9815698
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.91+7945C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815698 | ||||||
chr1:9815699
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7944C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815699 | ||||||
chr1:9815893
|
A | G | 171 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.91+7750T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815893 | ||||||
chr1:9815944
|
A | T | 9 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0180others(6): Show | 9 | HG00735.hp2 HG00738.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+7699T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815944 | ||||||
chr1:9815964
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+7679A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815964 | ||||||
chr1:9815981
|
C | T | 4 | a0001c0003t0004g0110a0001c0003t0004g0111a0001c0003t0004g0112others(1): Show | 4 | HG02451.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+7662G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9815981 | ||||||
chr1:9816050
|
G | A | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+7593C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816050 | ||||||
chr1:9816110
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.91+7533A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816110 | ||||||
chr1:9816536
|
TA | T | 29 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0164others(26): Show | 29 | HG00558.hp2 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.91+7106delT | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816536 | ||||||
chr1:9816537
|
A | T | 168 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.91+7106T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816537 | ||||||
chr1:9816538
|
A | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0164others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+7105T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816538 | ||||||
chr1:9816577
|
GTTTT | G | 145 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.91+7062_91+7065del others(4): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816577 | ||||||
chr1:9816590
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0246 | 2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.91+7053A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816590 | ||||||
chr1:9816675
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+6968A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816675 | ||||||
chr1:9816820
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+6823T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816820 | ||||||
chr1:9816906
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0161others(2): Show | 5 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+6737G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816906 | ||||||
chr1:9816936
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+6707G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9816936 | ||||||
chr1:9817094
|
C | T | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+6549G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817094 | ||||||
chr1:9817121
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+6522G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817121 | ||||||
chr1:9817130
|
G | A | 1 | a0002c0002t0002g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+6513C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817130 | ||||||
chr1:9817222
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.91+6421A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817222 | ||||||
chr1:9817247
|
A | C | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+6396T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817247 | ||||||
chr1:9817367
|
G | T | 1 | a0009c0012t0003g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.91+6276C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817367 | ||||||
chr1:9817686
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+5957C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817686 | ||||||
chr1:9817849
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+5794T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817849 | ||||||
chr1:9817864
|
G | A | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5779C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817864 | ||||||
chr1:9817920
|
G | C | 1 | a0002c0002t0003g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.91+5723C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817920 | ||||||
chr1:9817924
|
G | A | 1 | a0001c0003t0004g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+5719C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817924 | ||||||
chr1:9817930
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG01099.hp1 HG01978.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+5713G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9817930 | ||||||
chr1:9818003
|
CT | C | 239 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0124others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.91+5639delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818003 | ||||||
chr1:9818003
|
CTT | C | 11 | a0001c0001t0001g0248a0001c0003t0005g0099a0001c0006t0009g0266others(8): Show | 11 | HG00558.hp1 HG01243.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+5638_91+5639del others(2): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818003 | ||||||
chr1:9818105
|
T | G | 2 | a0002c0002t0002g0061a0002c0002t0002g0062 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91+5538A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818105 | ||||||
chr1:9818211
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+5432A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818211 | ||||||
chr1:9818249
|
G | A | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+5394C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818249 | ||||||
chr1:9818326
|
G | A | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5317C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818326 | ||||||
chr1:9818386
|
C | T | 36 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(33): Show | 36 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.91+5257G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818386 | ||||||
chr1:9818492
|
CTAATTTT others(2): Show |
C | 6 | a0001c0003t0005g0008a0001c0003t0005g0009a0001c0003t0005g0097others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+5142_91+5150del others(9): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818492 | ||||||
chr1:9818504
|
T | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+5139A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818504 | ||||||
chr1:9818532
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+5111A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818532 | ||||||
chr1:9818647
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91+4996C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818647 | ||||||
chr1:9818777
|
C | CT | 66 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(63): Show | 66 | HG00140.hp1 HG00423.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.91+4865dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | ||||||
chr1:9818777
|
CT | C | 19 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0003t0004g0110others(16): Show | 19 | HG00733.hp2 HG01257.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.91+4865delA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | ||||||
chr1:9818777
|
CTTT | C | 7 | a0003c0004t0002g0063a0003c0004t0002g0065a0003c0004t0002g0066others(4): Show | 7 | HG00558.hp1 HG01981.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+4863_91+4865del others(3): Show |
CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818777 | ||||||
chr1:9818850
|
G | A | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4793C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818850 | ||||||
chr1:9818856
|
G | A | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+4787C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818856 | ||||||
chr1:9818912
|
G | T | 12 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0012others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+4731C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818912 | ||||||
chr1:9818943
|
C | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4700G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818943 | ||||||
chr1:9818962
|
A | AT | 166 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.91+4680dupA | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9818962 | ||||||
chr1:9819026
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.91+4617G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819026 | ||||||
chr1:9819291
|
A | G | 2 | a0001c0003t0005g0008a0001c0003t0005g0009 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.91+4352T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819291 | ||||||
chr1:9819444
|
A | G | 1 | a0003c0004t0002g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+4199T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819444 | ||||||
chr1:9819559
|
A | G | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+4084T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819559 | ||||||
chr1:9819683
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+3960G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819683 | ||||||
chr1:9819686
|
G | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3957C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819686 | ||||||
chr1:9819707
|
T | C | 1 | a0001c0014t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+3936A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819707 | ||||||
chr1:9819754
|
T | C | 10 | a0001c0006t0009g0266a0001c0006t0009g0267a0003c0004t0002g0063others(7): Show | 10 | HG00558.hp1 HG01243.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+3889A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819754 | ||||||
chr1:9819896
|
C | A | 1 | a0001c0003t0004g0119 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+3747G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819896 | ||||||
chr1:9819975
|
A | G | 13 | a0001c0003t0004g0108a0001c0003t0004g0109a0001c0003t0004g0110others(10): Show | 13 | HG00733.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+3668T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9819975 | ||||||
chr1:9820159
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+3484G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820159 | ||||||
chr1:9820322
|
C | T | 1 | a0005c0011t0021g0270 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.91+3321G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820322 | ||||||
chr1:9820495
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.91+3148C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820495 | ||||||
chr1:9820517
|
A | T | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3126T>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820517 | ||||||
chr1:9820538
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.91+3105T>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820538 | ||||||
chr1:9820569
|
A | G | 1 | a0002c0002t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+3074T>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820569 | ||||||
chr1:9820572
|
T | G | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+3071A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820572 | ||||||
chr1:9820628
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+3015C>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820628 | ||||||
chr1:9820911
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0016g0259 | 3 | HG01099.hp2 HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.91+2732C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820911 | ||||||
chr1:9820917
|
T | C | 8 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0065others(5): Show | 8 | HG00558.hp1 HG01981.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+2726A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820917 | ||||||
chr1:9820983
|
G | A | 1 | a0001c0003t0004g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+2660C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9820983 | ||||||
chr1:9821054
|
C | T | 4 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0005others(1): Show | 4 | HG02717.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+2589G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821054 | ||||||
chr1:9821246
|
C | T | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+2397G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821246 | ||||||
chr1:9821314
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+2329C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821314 | ||||||
chr1:9821484
|
G | A | 146 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.91+2159C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821484 | ||||||
chr1:9821555
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.91+2088C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821555 | ||||||
chr1:9821636
|
T | C | 1 | a0001c0003t0004g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+2007A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821636 | ||||||
chr1:9821907
|
C | T | 165 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.91+1736G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821907 | ||||||
chr1:9821997
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+1646A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9821997 | ||||||
chr1:9822049
|
C | A | 165 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0125others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.91+1594G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822049 | ||||||
chr1:9822607
|
T | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.91+1036A>C | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822607 | ||||||
chr1:9822608
|
C | T | 78 | a0001c0001t0001g0106a0001c0003t0005g0008a0001c0003t0005g0009others(75): Show | 78 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.91+1035G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9822608 | ||||||
chr1:9823208
|
G | C | 1 | a0001c0003t0007g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+435C>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823208 | ||||||
chr1:9823226
|
T | A | 1 | a0001c0003t0006g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.91+417A>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823226 | ||||||
chr1:9823287
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.91+356C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823287 | ||||||
chr1:9823395
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.91+248G>A | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823395 | ||||||
chr1:9823419
|
T | C | 2 | a0001c0006t0009g0266a0001c0006t0009g0267 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+224A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823419 | ||||||
chr1:9823437
|
G | A | 4 | a0001c0003t0005g0097a0001c0003t0005g0098a0001c0003t0005g0099others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+206C>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823437 | ||||||
chr1:9823484
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+159A>G | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823484 | ||||||
chr1:9823609
|
C | A | 2 | a0002c0002t0002g0101a0002c0002t0002g0102 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.91+34G>T | CLSTN1 | ENSG00000171603.18 | transcript | ENST00000377298.9 | protein_coding | 1/18 | chr1 | 9823609 |