geneid | 84418 |
---|---|
ensemblid | ENSG00000120306.11 |
hgncid | 30239 |
symbol | CYSTM1 |
name | cysteine rich transmembrane module containing 1 |
refseq_nuc | NM_032412.4 |
refseq_prot | NP_115788.1 |
ensembl_nuc | ENST00000261811.6 |
ensembl_prot | ENSP00000261811.4 |
mane_status | MANE Select |
chr | chr5 |
start | 140175188 |
end | 140243789 |
strand | + |
ver | v1.2 |
region | chr5:140175188-140243789 |
region5000 | chr5:140170188-140248789 |
regionname0 | CYSTM1_chr5_140175188_140243789 |
regionname5000 | CYSTM1_chr5_140170188_140248789 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 97 | 324 | 76 | 58 | 146 | 10 | 32 | 120 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 294 | 324 | 76 | 58 | 146 | 10 | 32 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 497 | 226 | 64 | 44 | 90 | 5 | 21 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
t0002 | 0/0 | 497 | 48 | 2 | 7 | 30 | 4 | 5 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
t0003 | 0/0 | 497 | 47 | 9 | 7 | 26 | 1 | 4 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
t0004 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
t0005 | 0/0 | 497 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
t0006 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 294 | 324 | 76 | 58 | 146 | 10 | 32 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 790 | 226 | 64 | 44 | 90 | 5 | 21 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
a0001c0001t0002 | 0/0 | 790 | 48 | 2 | 7 | 30 | 4 | 5 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
a0001c0001t0003 | 0/0 | 790 | 47 | 9 | 7 | 26 | 1 | 4 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
a0001c0001t0004 | 0/0 | 790 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
a0001c0001t0005 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
a0001c0001t0006 | 0/0 | 790 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | copy fasta | chr5 | 140170188 | 140248789 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | GBR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | FIN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0141 | EUR | FIN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0271 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0303 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0097 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0137 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | BEB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | TSI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | TSI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | USA | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0051 | REF | REF | CYSTM1_chr5_140170188_140248789 | CYSTM1 | chr5 | 140170188 | 140248789 |
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 |
---|
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 |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:140175265
|
G | C | 1 | a0001c0001t0004 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/3 | 19201 | chr5 | 140175265 | |||||
chr5:140175281
|
G | C | 1 | a0001c0001t0002 | 48 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/3 | 19185 | chr5 | 140175281 | |||||
chr5:140194465
|
G | A | 2 | a0001c0001t0002a0001c0001t0003 | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/3 | 1 | chr5 | 140194465 | |||||
chr5:140243427
|
C | T | 1 | a0001c0001t0006 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 3/3 | 16 | chr5 | 140243427 | |||||
chr5:140243769
|
A | G | 1 | a0001c0001t0005 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 3/3 | 358 | chr5 | 140243769 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:140175299
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-21+14G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140175299 | ||||||
chr5:140175534
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21+249T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140175534 | ||||||
chr5:140175778
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21+493G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140175778 | ||||||
chr5:140176358
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-21+1073T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140176358 | ||||||
chr5:140176582
|
A | G | 2 | a0001c0001t0003g0302a0001c0001t0003g0303 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-21+1297A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140176582 | ||||||
chr5:140176843
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(219): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-21+1558A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140176843 | ||||||
chr5:140176913
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+1628T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140176913 | ||||||
chr5:140177063
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+1778T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177063 | ||||||
chr5:140177067
|
T | TCAAAAAA others(16): Show |
1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21+1794_-21+1795i others(25): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177067 | |||||
chr5:140177068
|
C | CAAA | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(91): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-21+1800_-21+1802d others(5): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177068 | |||||
chr5:140177068
|
C | CAAAA | 15 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(12): Show | 15 | HG00621.hp2 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21+1799_-21+1802d others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177068 | |||||
chr5:140177068
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-21+1790_-21+1802d others(15): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177068 | |||||
chr5:140177069
|
A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+1794_-21+1795i others(24): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177069 | |||||
chr5:140177073
|
A | AAAAAAAC others(15): Show |
1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-21+1794_-21+1795i others(24): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177073 | |||||
chr5:140177078
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01934.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-21+1802_-21+1803i others(17): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177078 | |||||
chr5:140177078
|
A | AAAAAAAA others(7): Show |
15 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0111others(12): Show | 15 | HG00621.hp1 HG01175.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21+1802_-21+1803i others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177078 | |||||
chr5:140177078
|
A | AAAAAAAA others(6): Show |
64 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(61): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21+1802_-21+1803i others(15): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177078 | |||||
chr5:140177078
|
A | AAAAAAAA others(5): Show |
6 | a0001c0001t0002g0176a0001c0001t0003g0177a0001c0001t0003g0178others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+1802_-21+1803i others(14): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177078 | |||||
chr5:140177078
|
A | AAAAACAA others(6): Show |
1 | a0001c0001t0003g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-21+1797_-21+1798i others(15): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140177078 | |||||
chr5:140177084
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21+1799A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177084 | ||||||
chr5:140177592
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-21+2307G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177592 | ||||||
chr5:140177614
|
C | T | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-21+2329C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177614 | ||||||
chr5:140177647
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-21+2362A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177647 | ||||||
chr5:140177672
|
G | A | 8 | a0001c0001t0003g0104a0001c0001t0003g0118a0001c0001t0003g0119others(5): Show | 8 | NA18951.hp1 NA18957.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+2387G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177672 | ||||||
chr5:140177800
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(109): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-21+2515C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177800 | ||||||
chr5:140177853
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21+2568A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177853 | ||||||
chr5:140177860
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+2575G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177860 | ||||||
chr5:140177928
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-21+2643A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140177928 | ||||||
chr5:140178243
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-21+2958T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178243 | ||||||
chr5:140178441
|
C | CT | 15 | a0001c0001t0001g0021a0001c0001t0001g0086a0001c0001t0001g0087others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21+3181dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0188others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+3172_-21+3181d others(12): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-21+3171_-21+3181d others(13): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-21+3170_-21+3181d others(14): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0002g0126others(5): Show | 8 | HG00558.hp2 HG01070.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+3168_-21+3181d others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(8): Show |
37 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(34): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-21+3167_-21+3181d others(17): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(9): Show |
36 | a0001c0001t0001g0019a0001c0001t0002g0111a0001c0001t0002g0112others(33): Show | 37 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21+3166_-21+3181d others(18): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174others(3): Show | 6 | HG01361.hp2 HG01934.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+3165_-21+3181d others(19): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+3164_-21+3181d others(20): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
CT | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 70 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.-21+3181delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178441
|
CTT | C | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 50 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-21+3180_-21+3181d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140178441 | |||||
chr5:140178466
|
T | TTTTTTTT others(10): Show |
1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-21+3181_-21+3182i others(19): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178466 | ||||||
chr5:140178627
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+3342T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178627 | ||||||
chr5:140178808
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-21+3523C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178808 | ||||||
chr5:140178827
|
C | T | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-21+3542C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178827 | ||||||
chr5:140178911
|
G | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+3626G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178911 | ||||||
chr5:140178999
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(108): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-21+3714C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140178999 | ||||||
chr5:140179000
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21+3715G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179000 | ||||||
chr5:140179084
|
C | T | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-21+3799C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179084 | ||||||
chr5:140179108
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-21+3823A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179108 | ||||||
chr5:140179223
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(109): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-21+3938G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179223 | ||||||
chr5:140179261
|
TA | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+3990delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140179261 | |||||
chr5:140179280
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-21+3995T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179280 | ||||||
chr5:140179335
|
G | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+4050G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179335 | ||||||
chr5:140179357
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-21+4072G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179357 | ||||||
chr5:140179429
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(108): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-21+4144T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179429 | ||||||
chr5:140179431
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-21+4146C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179431 | ||||||
chr5:140179514
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-21+4229T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179514 | ||||||
chr5:140179669
|
C | CTTTTCTT | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-21+4387_-21+4393d others(9): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140179669 | |||||
chr5:140179909
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-21+4624C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140179909 | ||||||
chr5:140180332
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+5047T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180332 | ||||||
chr5:140180566
|
A | C | 1 | a0001c0001t0003g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-21+5281A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180566 | ||||||
chr5:140180567
|
T | A | 1 | a0001c0001t0003g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-21+5282T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180567 | ||||||
chr5:140180729
|
G | T | 1 | a0001c0001t0001g0283 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-21+5444G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180729 | ||||||
chr5:140180765
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-21+5480T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180765 | ||||||
chr5:140180913
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+5628T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180913 | ||||||
chr5:140180943
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-21+5658T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140180943 | ||||||
chr5:140181065
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG01884.hp1 NA18942.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+5780T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181065 | ||||||
chr5:140181109
|
G | A | 7 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(4): Show | 7 | HG01884.hp1 HG01934.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21+5824G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181109 | ||||||
chr5:140181221
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-21+5936G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181221 | ||||||
chr5:140181352
|
C | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-21+6067C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181352 | ||||||
chr5:140181431
|
G | A | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(80): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-21+6146G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181431 | ||||||
chr5:140181928
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG01928.hp2 HG01943.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+6643C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140181928 | ||||||
chr5:140182044
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-21+6759G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182044 | ||||||
chr5:140182145
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0194 | 5 | HG02738.hp1 HG03490.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+6860T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182145 | ||||||
chr5:140182212
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-21+6927C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182212 | ||||||
chr5:140182321
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+7036G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182321 | ||||||
chr5:140182629
|
C | CT | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG01952.hp2 HG02071.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+7357dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140182629 | |||||
chr5:140182642
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0194others(1): Show | 6 | HG02056.hp1 HG02738.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+7357T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182642 | ||||||
chr5:140182656
|
C | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-21+7371C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182656 | ||||||
chr5:140182656
|
CCCAAACT others(10): Show |
C | 1 | a0001c0001t0003g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-21+7374_-21+7390d others(19): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140182656 | |||||
chr5:140182700
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-21+7415G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182700 | ||||||
chr5:140182921
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-21+7636C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182921 | ||||||
chr5:140182922
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-21+7637C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182922 | ||||||
chr5:140182989
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-21+7704G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140182989 | ||||||
chr5:140183116
|
T | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+7831T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183116 | ||||||
chr5:140183157
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-21+7872G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183157 | ||||||
chr5:140183206
|
A | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0193a0001c0001t0001g0197others(10): Show | 14 | HG00323.hp1 HG01192.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+7921A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183206 | ||||||
chr5:140183236
|
C | G | 1 | a0001c0001t0003g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-21+7951C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183236 | ||||||
chr5:140183246
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-21+7961G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183246 | ||||||
chr5:140183406
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-21+8121C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183406 | ||||||
chr5:140183623
|
G | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-21+8338G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183623 | ||||||
chr5:140183713
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-21+8428C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183713 | ||||||
chr5:140183837
|
C | A | 1 | a0001c0001t0001g0246 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-21+8552C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183837 | ||||||
chr5:140183898
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21+8613T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140183898 | ||||||
chr5:140184094
|
T | TAATATA | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(219): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-21+8812_-21+8813i others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140184094 | |||||
chr5:140184318
|
A | G | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+9033A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184318 | ||||||
chr5:140184342
|
T | TTGATGAA others(12): Show |
1 | a0001c0001t0002g0108 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-21+9059_-21+9077d others(21): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140184342 | |||||
chr5:140184387
|
G | GT | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(114): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-21+9114dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140184387 | |||||
chr5:140184494
|
G | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0128a0001c0001t0002g0146others(3): Show | 7 | HG00438.hp1 NA18942.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+9209G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184494 | ||||||
chr5:140184515
|
T | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | NA18941.hp1 NA18988.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+9230T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184515 | ||||||
chr5:140184806
|
A | G | 6 | a0001c0001t0003g0109a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 6 | HG01952.hp2 HG02071.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+9521A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184806 | ||||||
chr5:140184888
|
G | A | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-20-9558G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184888 | ||||||
chr5:140184928
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-20-9518A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184928 | ||||||
chr5:140184932
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-9514A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140184932 | ||||||
chr5:140185006
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-20-9440T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185006 | ||||||
chr5:140185144
|
T | A | 7 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0248others(4): Show | 7 | HG02027.hp2 NA18949.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-9302T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185144 | ||||||
chr5:140185321
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-20-9125A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185321 | ||||||
chr5:140185436
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-20-9010T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185436 | ||||||
chr5:140185443
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-9003A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185443 | ||||||
chr5:140185505
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-8941G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185505 | ||||||
chr5:140185561
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-8885A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185561 | ||||||
chr5:140185628
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-8818G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185628 | ||||||
chr5:140185631
|
A | T | 1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20-8815A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185631 | ||||||
chr5:140185660
|
G | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-8786G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185660 | ||||||
chr5:140185760
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0165 | 2 | NA18943.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-20-8686A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185760 | ||||||
chr5:140185851
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-20-8595T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140185851 | ||||||
chr5:140186028
|
T | C | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0283others(1): Show | 4 | NA18955.hp1 NA18992.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-8418T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186028 | ||||||
chr5:140186049
|
C | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-8397C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186049 | ||||||
chr5:140186130
|
CTA | C | 88 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-20-8311_-20-8310d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140186130 | |||||
chr5:140186156
|
C | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-8290C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186156 | ||||||
chr5:140186521
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-20-7925G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186521 | ||||||
chr5:140186771
|
A | AAT | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(55): Show | 67 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.-20-7672_-20-7671d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140186771 | |||||
chr5:140186917
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-20-7529G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186917 | ||||||
chr5:140186976
|
A | G | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-7470A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140186976 | ||||||
chr5:140187003
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-7443G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187003 | ||||||
chr5:140187080
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-20-7366C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187080 | ||||||
chr5:140187091
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0194 | 5 | HG02738.hp1 HG03490.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-7355C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187091 | ||||||
chr5:140187171
|
CT | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(211): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-20-7261delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140187171 | |||||
chr5:140187302
|
T | TA | 10 | a0001c0001t0001g0035a0001c0001t0001g0195a0001c0001t0001g0198others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20-7130dupA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140187302 | |||||
chr5:140187433
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0080 | 2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-20-7013C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187433 | ||||||
chr5:140187632
|
G | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-20-6814G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187632 | ||||||
chr5:140187879
|
A | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 9 | HG00323.hp1 HG01192.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20-6567A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187879 | ||||||
chr5:140187942
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-20-6504A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187942 | ||||||
chr5:140187951
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-6495G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140187951 | ||||||
chr5:140188019
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-6427A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188019 | ||||||
chr5:140188070
|
C | CT | 105 | a0001c0001t0001g0078a0001c0001t0001g0182a0001c0001t0001g0183others(102): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-20-6358dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140188070 | |||||
chr5:140188111
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-6335T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188111 | ||||||
chr5:140188408
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-20-6038A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188408 | ||||||
chr5:140188469
|
C | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-5977C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188469 | ||||||
chr5:140188685
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20-5761A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188685 | ||||||
chr5:140188778
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(115): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-20-5650dupA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140188778 | |||||
chr5:140188778
|
C | CAA | 90 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-20-5651_-20-5650d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140188778 | |||||
chr5:140188900
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-5546T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188900 | ||||||
chr5:140188929
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-20-5517A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140188929 | ||||||
chr5:140189177
|
A | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-5269A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140189177 | ||||||
chr5:140189179
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-5267G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140189179 | ||||||
chr5:140189394
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-20-5052A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140189394 | ||||||
chr5:140189554
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-20-4892T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140189554 | ||||||
chr5:140189996
|
A | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-20-4450A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140189996 | ||||||
chr5:140190274
|
C | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-20-4172C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140190274 | ||||||
chr5:140190320
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-4126T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140190320 | ||||||
chr5:140190327
|
G | GT | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-4113dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140190327 | |||||
chr5:140190454
|
C | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3992C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140190454 | ||||||
chr5:140190475
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-20-3971A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140190475 | ||||||
chr5:140191080
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0287 | 3 | NA18945.hp2 NA18985.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-20-3366A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191080 | ||||||
chr5:140191146
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-20-3300G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191146 | ||||||
chr5:140191297
|
A | G | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-3149A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191297 | ||||||
chr5:140191388
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-20-3058C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191388 | ||||||
chr5:140191703
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-20-2743G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191703 | ||||||
chr5:140191809
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG00673.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-20-2637A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191809 | ||||||
chr5:140191871
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01928.hp1 NA18961.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-20-2575A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140191871 | ||||||
chr5:140192009
|
C | T | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-2437C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192009 | ||||||
chr5:140192031
|
A | G | 3 | a0001c0001t0002g0125a0001c0001t0002g0163a0001c0001t0002g0171 | 3 | HG03490.hp2 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-20-2415A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192031 | ||||||
chr5:140192140
|
A | G | 1 | a0001c0001t0002g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-20-2306A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192140 | ||||||
chr5:140192213
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-20-2233A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192213 | ||||||
chr5:140192320
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0254 | 3 | HG00673.hp1 NA18944.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-20-2126C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192320 | ||||||
chr5:140192350
|
A | G | 1 | a0001c0001t0003g0123 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-20-2096A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192350 | ||||||
chr5:140192505
|
G | T | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-20-1941G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140192505 | ||||||
chr5:140193122
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-20-1324C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140193122 | ||||||
chr5:140193233
|
G | A | 1 | a0001c0001t0003g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20-1213G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140193233 | ||||||
chr5:140193269
|
A | ATTGT | 7 | a0001c0001t0001g0036a0001c0001t0002g0007a0001c0001t0002g0128others(4): Show | 8 | HG00438.hp1 NA18942.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-1150_-20-1147d others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140193269 | |||||
chr5:140193269
|
ATTGT | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(113): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-20-1150_-20-1147d others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 140193269 | |||||
chr5:140193680
|
A | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-20-766A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140193680 | ||||||
chr5:140193820
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20-626C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140193820 | ||||||
chr5:140194165
|
C | T | 1 | a0001c0001t0004g0271 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-20-281C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140194165 | ||||||
chr5:140194175
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20-271C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140194175 | ||||||
chr5:140194368
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-20-78G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 1/2 | chr5 | 140194368 | ||||||
chr5:140194692
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG00673.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.187+40A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140194692 | ||||||
chr5:140195105
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+453G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195105 | ||||||
chr5:140195439
|
C | CT | 91 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.187+807dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140195439 | |||||
chr5:140195439
|
C | CTT | 7 | a0001c0001t0002g0141a0001c0001t0002g0152a0001c0001t0002g0167others(4): Show | 7 | HG00323.hp2 HG02559.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+806_187+807dup others(2): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140195439 | |||||
chr5:140195439
|
CT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(111): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.187+807delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140195439 | |||||
chr5:140195491
|
A | G | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.187+839A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195491 | ||||||
chr5:140195503
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG00642.hp1 HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.187+851G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195503 | ||||||
chr5:140195543
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.187+891G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195543 | ||||||
chr5:140195603
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0269 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.187+951G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195603 | ||||||
chr5:140195688
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+1036T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140195688 | ||||||
chr5:140196005
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+1353A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196005 | ||||||
chr5:140196024
|
C | CAG | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+1373_187+1374d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140196024 | |||||
chr5:140196088
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.187+1436T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196088 | ||||||
chr5:140196292
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1640C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196292 | ||||||
chr5:140196390
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.187+1738C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196390 | ||||||
chr5:140196432
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.187+1780T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196432 | ||||||
chr5:140196464
|
T | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+1812T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196464 | ||||||
chr5:140196587
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1935A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196587 | ||||||
chr5:140196758
|
AG | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2107delG | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196758 | ||||||
chr5:140196762
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+2110T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196762 | ||||||
chr5:140196900
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.187+2248A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196900 | ||||||
chr5:140196970
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.187+2318A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140196970 | ||||||
chr5:140197157
|
A | G | 3 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG01243.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.187+2505A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197157 | ||||||
chr5:140197157
|
A | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0079 | 3 | NA19004.hp1 NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.187+2505A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197157 | ||||||
chr5:140197263
|
C | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0269 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.187+2611C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197263 | ||||||
chr5:140197338
|
G | C | 1 | a0001c0001t0002g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.187+2686G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197338 | ||||||
chr5:140197634
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.187+2982T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197634 | ||||||
chr5:140197789
|
TA | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(108): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+3138delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140197789 | ||||||
chr5:140198291
|
CAAT | C | 24 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 24 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.187+3640_187+3642d others(5): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140198291 | ||||||
chr5:140198707
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.187+4055T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140198707 | ||||||
chr5:140199212
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.187+4560G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199212 | ||||||
chr5:140199474
|
T | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+4822T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199474 | ||||||
chr5:140199525
|
CTG | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG02056.hp2 NA18747.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4875_187+4876d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140199525 | |||||
chr5:140199665
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.187+5013T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199665 | ||||||
chr5:140199754
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(215): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.187+5102T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199754 | ||||||
chr5:140199804
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.187+5152T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199804 | ||||||
chr5:140199836
|
C | G | 81 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(78): Show | 85 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.187+5184C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140199836 | ||||||
chr5:140200102
|
T | TG | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(110): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.187+5451dupG | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200102 | |||||
chr5:140200260
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.187+5608C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200260 | ||||||
chr5:140200300
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187+5648A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200300 | ||||||
chr5:140200557
|
C | CT | 16 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0040others(13): Show | 16 | HG01175.hp1 HG01256.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.187+5926dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
C | CTTTTTTT | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.187+5920_187+5926d others(9): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
C | CTTTTTTT others(1): Show |
26 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0115others(23): Show | 26 | HG00423.hp1 HG01106.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.187+5919_187+5926d others(10): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.187+5913_187+5926d others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.187+5912_187+5926d others(17): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.187+5911_187+5926d others(18): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200557
|
CT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(101): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.187+5926delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140200557 | |||||
chr5:140200637
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.187+5985T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200637 | ||||||
chr5:140200653
|
C | T | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+6001C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200653 | ||||||
chr5:140200664
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0170 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187+6012C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200664 | ||||||
chr5:140200674
|
C | A | 20 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0108others(17): Show | 22 | HG00099.hp1 HG00438.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.187+6022C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200674 | ||||||
chr5:140200729
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.187+6077T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140200729 | ||||||
chr5:140201218
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0301 | 2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.187+6566C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201218 | ||||||
chr5:140201259
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+6607A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201259 | ||||||
chr5:140201344
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.187+6692G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201344 | ||||||
chr5:140201461
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187+6809T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201461 | ||||||
chr5:140201620
|
T | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.187+6968T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201620 | ||||||
chr5:140201669
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+7017C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201669 | ||||||
chr5:140201723
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.187+7071T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201723 | ||||||
chr5:140201932
|
C | CT | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG01175.hp1 HG01358.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+7303dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140201932 | |||||
chr5:140201932
|
CT | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(166): Show | 184 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.187+7303delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140201932 | |||||
chr5:140201932
|
CTT | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.187+7302_187+7303d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140201932 | |||||
chr5:140201976
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+7324T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140201976 | ||||||
chr5:140202061
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.187+7409G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202061 | ||||||
chr5:140202142
|
G | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(55): Show | 67 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.187+7490G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202142 | ||||||
chr5:140202183
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(216): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.187+7531T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202183 | ||||||
chr5:140202188
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(108): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+7536G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202188 | ||||||
chr5:140202328
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.187+7676G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202328 | ||||||
chr5:140202572
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.187+7920G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202572 | ||||||
chr5:140202620
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.187+7968C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202620 | ||||||
chr5:140202801
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+8149T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202801 | ||||||
chr5:140202914
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+8262C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202914 | ||||||
chr5:140202925
|
C | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+8273C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140202925 | ||||||
chr5:140202983
|
G | GA | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+8340dupA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140202983 | |||||
chr5:140203105
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+8453G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140203105 | ||||||
chr5:140203687
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.187+9035C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140203687 | ||||||
chr5:140203771
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.187+9119C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140203771 | ||||||
chr5:140204075
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.187+9423T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204075 | ||||||
chr5:140204131
|
C | T | 1 | a0001c0001t0003g0004 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.187+9479C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204131 | ||||||
chr5:140204143
|
C | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+9491C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204143 | ||||||
chr5:140204165
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0298 | 3 | NA18969.hp2 NA19077.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187+9513G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204165 | ||||||
chr5:140204197
|
C | T | 2 | a0001c0001t0003g0117a0001c0001t0003g0150 | 2 | HG01934.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.187+9545C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204197 | ||||||
chr5:140204344
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186 | 3 | HG02572.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.187+9692G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204344 | ||||||
chr5:140204569
|
TATAAC | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+9919_187+9923d others(7): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140204569 | |||||
chr5:140204622
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+9970G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204622 | ||||||
chr5:140204622
|
G | T | 3 | a0001c0001t0003g0110a0001c0001t0003g0127a0001c0001t0003g0164 | 3 | HG00558.hp2 HG02027.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.187+9970G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204622 | ||||||
chr5:140204690
|
C | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(109): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.187+10038C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204690 | ||||||
chr5:140204767
|
C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+10115C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204767 | ||||||
chr5:140204774
|
C | CGT | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+10133_187+1013 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140204774 | |||||
chr5:140204774
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.187+10122C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204774 | ||||||
chr5:140204879
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.187+10227G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140204879 | ||||||
chr5:140205199
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+10547C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140205199 | ||||||
chr5:140205351
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.187+10699C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140205351 | ||||||
chr5:140205520
|
T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+10868T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140205520 | ||||||
chr5:140205624
|
C | G | 1 | a0001c0001t0002g0144 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.187+10972C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140205624 | ||||||
chr5:140206048
|
T | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+11396T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206048 | ||||||
chr5:140206241
|
C | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+11589C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206241 | ||||||
chr5:140206529
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.187+11877A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206529 | ||||||
chr5:140206568
|
T | A | 1 | a0001c0001t0001g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.187+11916T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206568 | ||||||
chr5:140206607
|
G | GTTGT | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(94): Show | 110 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.187+11986_187+1198 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206607 | |||||
chr5:140206607
|
G | GTTGTTTG others(1): Show |
11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0226others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.187+11982_187+1198 others(12): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206607 | |||||
chr5:140206607
|
G | GTTGTTTG others(5): Show |
3 | a0001c0001t0001g0197a0001c0001t0001g0206a0001c0001t0001g0274 | 3 | HG02280.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.187+11978_187+1198 others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206607 | |||||
chr5:140206607
|
GTTGT | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0182a0001c0001t0001g0294others(2): Show | 5 | HG01978.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+11986_187+1198 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206607 | |||||
chr5:140206607
|
GTTGTTTG others(5): Show |
G | 2 | a0001c0001t0003g0117a0001c0001t0003g0150 | 2 | HG01934.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.187+11978_187+1198 others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206607 | |||||
chr5:140206638
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.187+11986G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206638 | ||||||
chr5:140206638
|
G | GTTTC | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+11990_187+1199 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140206638 | |||||
chr5:140206666
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.187+12014T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206666 | ||||||
chr5:140206706
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+12054C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206706 | ||||||
chr5:140206792
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.187+12140A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206792 | ||||||
chr5:140206884
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+12232C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206884 | ||||||
chr5:140206916
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(108): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+12264G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140206916 | ||||||
chr5:140207149
|
C | G | 1 | a0001c0001t0002g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.187+12497C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140207149 | ||||||
chr5:140207566
|
T | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | NA18942.hp2 NA18953.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.187+12914T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140207566 | ||||||
chr5:140207809
|
A | G | 8 | a0001c0001t0003g0110a0001c0001t0003g0113a0001c0001t0003g0124others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+13157A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140207809 | ||||||
chr5:140207949
|
G | A | 2 | a0001c0001t0003g0117a0001c0001t0003g0150 | 2 | HG01934.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.187+13297G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140207949 | ||||||
chr5:140208133
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.187+13481C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140208133 | ||||||
chr5:140208186
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.187+13534A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140208186 | ||||||
chr5:140208353
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.187+13701T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140208353 | ||||||
chr5:140208732
|
T | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+14080T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140208732 | ||||||
chr5:140209038
|
CA | C | 12 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0216others(9): Show | 12 | HG02258.hp2 HG02559.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+14401delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140209038 | |||||
chr5:140209047
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.187+14395A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209047 | ||||||
chr5:140209250
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+14598C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209250 | ||||||
chr5:140209261
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.187+14609T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209261 | ||||||
chr5:140209269
|
CT | C | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(103): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.187+14632delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140209269 | |||||
chr5:140209353
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.187+14701G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209353 | ||||||
chr5:140209433
|
A | AT | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(5): Show | 10 | HG02280.hp1 HG02738.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+14795dupT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140209433 | |||||
chr5:140209617
|
GC | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(77): Show | 81 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+14966delC | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209617 | ||||||
chr5:140209650
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.187+14998G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209650 | ||||||
chr5:140209724
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(188): Show | 198 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.187+15072A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209724 | ||||||
chr5:140209849
|
C | T | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+15197C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209849 | ||||||
chr5:140209992
|
A | T | 1 | a0001c0001t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.187+15340A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140209992 | ||||||
chr5:140210081
|
A | T | 1 | a0001c0001t0001g0270 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.187+15429A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210081 | ||||||
chr5:140210110
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01928.hp1 NA18961.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.187+15458C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210110 | ||||||
chr5:140210519
|
CT | C | 190 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(187): Show | 197 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.187+15879delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140210519 | |||||
chr5:140210659
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+16007G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210659 | ||||||
chr5:140210665
|
C | T | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+16013C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210665 | ||||||
chr5:140210704
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(38): Show | 49 | HG00408.hp1 HG00673.hp1 HG01952.hp1 others(46): Show |
intron_variant | MODIFIER | c.187+16052G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210704 | ||||||
chr5:140210928
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.187+16276A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140210928 | ||||||
chr5:140211141
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 9 | HG00323.hp1 HG01192.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+16489G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211141 | ||||||
chr5:140211205
|
C | A | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+16553C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211205 | ||||||
chr5:140211281
|
T | C | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.187+16629T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211281 | ||||||
chr5:140211470
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.187+16818T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211470 | ||||||
chr5:140211549
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+16897G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211549 | ||||||
chr5:140211685
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0003g0170 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187+17033G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140211685 | ||||||
chr5:140212042
|
A | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.187+17390A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212042 | ||||||
chr5:140212142
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+17490A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212142 | ||||||
chr5:140212196
|
T | G | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+17544T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212196 | ||||||
chr5:140212265
|
C | T | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+17613C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212265 | ||||||
chr5:140212397
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.187+17745C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212397 | ||||||
chr5:140212729
|
G | A | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(80): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+18077G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212729 | ||||||
chr5:140212983
|
G | GTA | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0193others(21): Show | 26 | HG00280.hp2 HG00323.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+18357_187+1835 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATA | 12 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0001g0212others(9): Show | 13 | HG00099.hp2 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+18355_187+1835 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATATA | 5 | a0001c0001t0001g0215a0001c0001t0001g0260a0001c0001t0001g0285others(2): Show | 5 | HG00642.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+18353_187+1835 others(10): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.187+18339_187+1835 others(24): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.187+18337_187+1835 others(26): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+18335_187+1835 others(28): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.187+18358_187+1835 others(34): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0001g0029 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.187+18332_187+1833 others(14): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(7): Show |
6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0084others(3): Show | 6 | HG02129.hp2 HG02622.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(18): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(9): Show |
10 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0039others(7): Show | 10 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(20): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(11): Show |
27 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(24): Show | 27 | HG01074.hp2 HG01081.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(22): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(13): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0027others(12): Show | 16 | HG00423.hp2 HG01255.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(24): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(15): Show |
1 | a0001c0001t0001g0040 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.187+18332_187+1833 others(26): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(17): Show |
7 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0044others(4): Show | 7 | HG01175.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(28): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(19): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00558.hp1 HG02080.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+18332_187+1833 others(30): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(21): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0060 | 2 | HG01978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.187+18332_187+1833 others(32): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
G | GTGTATAT others(23): Show |
1 | a0001c0001t0001g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+18332_187+1833 others(34): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
GTATA | G | 9 | a0001c0001t0001g0182a0001c0001t0002g0111a0001c0001t0002g0114others(6): Show | 9 | HG00280.hp1 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+18355_187+1835 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212983
|
GTATATA | G | 91 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(88): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.187+18353_187+1835 others(10): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140212983 | |||||
chr5:140212985
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0050others(3): Show | 6 | HG02083.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+18333A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212985 | ||||||
chr5:140212996
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.187+18345_187+1836 others(20): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212996 | ||||||
chr5:140212998
|
TATATATA others(7): Show |
T | 5 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | HG02630.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+18347_187+1836 others(18): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140212998 | ||||||
chr5:140213011
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(72): Show | 76 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.187+18359G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213011 | ||||||
chr5:140213012
|
A | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(72): Show | 76 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.187+18360A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213012 | ||||||
chr5:140213056
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.187+18404A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213056 | ||||||
chr5:140213157
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187+18505A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213157 | ||||||
chr5:140213192
|
T | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187+18540T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213192 | ||||||
chr5:140213239
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187+18587G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213239 | ||||||
chr5:140213259
|
T | A | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.187+18607T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213259 | ||||||
chr5:140213587
|
C | T | 6 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+18935C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213587 | ||||||
chr5:140213602
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.187+18950C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213602 | ||||||
chr5:140213630
|
A | T | 1 | a0001c0001t0003g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.187+18978A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140213630 | ||||||
chr5:140214506
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+19854T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140214506 | ||||||
chr5:140214564
|
G | C | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+19912G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140214564 | ||||||
chr5:140214630
|
TA | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.187+19984delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140214630 | |||||
chr5:140214762
|
GGCA | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+20111_187+2011 others(7): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140214762 | ||||||
chr5:140215050
|
A | C | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20398A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215050 | ||||||
chr5:140215054
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20402T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215054 | ||||||
chr5:140215058
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20406C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215058 | ||||||
chr5:140215059
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20407A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215059 | ||||||
chr5:140215061
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20409T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215061 | ||||||
chr5:140215062
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20410G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215062 | ||||||
chr5:140215064
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20412T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215064 | ||||||
chr5:140215065
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20413C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215065 | ||||||
chr5:140215066
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.187+20414A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215066 | ||||||
chr5:140215542
|
T | TTAAATTA others(320): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0057 | 2 | NA18970.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.187+20901_187+2090 others(331): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140215542 | |||||
chr5:140215542
|
T | TTAAATTA others(321): Show |
1 | a0001c0001t0001g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.187+20901_187+2090 others(332): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140215542 | |||||
chr5:140215542
|
T | TTAAATTA others(320): Show |
45 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0020others(42): Show | 47 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.187+20901_187+2090 others(331): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140215542 | |||||
chr5:140215542
|
T | TTAAATTA others(321): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0090 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.187+20901_187+2090 others(332): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140215542 | |||||
chr5:140215542
|
T | TTAAATTA others(320): Show |
34 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 34 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.187+20901_187+2090 others(331): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140215542 | |||||
chr5:140215714
|
C | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+21062C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215714 | ||||||
chr5:140215772
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187+21120T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140215772 | ||||||
chr5:140216029
|
A | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+21377A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216029 | ||||||
chr5:140216032
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.187+21380T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216032 | ||||||
chr5:140216037
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(52): Show | 56 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.187+21385G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216037 | ||||||
chr5:140216087
|
A | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+21435A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216087 | ||||||
chr5:140216141
|
C | CA | 7 | a0001c0001t0001g0038a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+21500dupA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140216141 | |||||
chr5:140216166
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+21514T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216166 | ||||||
chr5:140216479
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG02056.hp2 NA18747.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+21827G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216479 | ||||||
chr5:140216625
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.187+21973A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216625 | ||||||
chr5:140216798
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.187+22146T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216798 | ||||||
chr5:140216887
|
G | C | 1 | a0001c0001t0003g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.187+22235G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216887 | ||||||
chr5:140216887
|
G | GAC | 100 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(97): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.187+22251_187+2225 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140216887 | |||||
chr5:140216967
|
C | T | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.187+22315C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140216967 | ||||||
chr5:140217154
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0080 | 3 | HG01256.hp1 HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.187+22502A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140217154 | ||||||
chr5:140217208
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+22556C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140217208 | ||||||
chr5:140217576
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.187+22924A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140217576 | ||||||
chr5:140217591
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+22939C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140217591 | ||||||
chr5:140217995
|
T | G | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(80): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+23343T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140217995 | ||||||
chr5:140218072
|
C | T | 8 | a0001c0001t0003g0110a0001c0001t0003g0113a0001c0001t0003g0124others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+23420C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140218072 | ||||||
chr5:140218325
|
C | T | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.187+23673C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140218325 | ||||||
chr5:140218505
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.187+23853A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140218505 | ||||||
chr5:140219157
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-24148T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219157 | ||||||
chr5:140219288
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-24017C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219288 | ||||||
chr5:140219319
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.188-23986G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219319 | ||||||
chr5:140219387
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.188-23918G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219387 | ||||||
chr5:140219512
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(185): Show | 195 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.188-23793T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219512 | ||||||
chr5:140219549
|
G | A | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.188-23756G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219549 | ||||||
chr5:140219734
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-23571T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219734 | ||||||
chr5:140219831
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.188-23474A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219831 | ||||||
chr5:140219832
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.188-23473T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140219832 | ||||||
chr5:140220014
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.188-23291T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140220014 | ||||||
chr5:140220316
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.188-22989G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140220316 | ||||||
chr5:140220435
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-22870A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140220435 | ||||||
chr5:140220553
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-22752T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140220553 | ||||||
chr5:140221287
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.188-22018T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221287 | ||||||
chr5:140221297
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.188-22008G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221297 | ||||||
chr5:140221367
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-21938C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221367 | ||||||
chr5:140221412
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.188-21893C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221412 | ||||||
chr5:140221512
|
C | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-21793C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221512 | ||||||
chr5:140221921
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0208 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.188-21384C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140221921 | ||||||
chr5:140222097
|
A | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | NA18944.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.188-21208A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140222097 | ||||||
chr5:140222354
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-20951C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140222354 | ||||||
chr5:140222614
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-20691C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140222614 | ||||||
chr5:140222809
|
G | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(79): Show | 84 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.188-20496G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140222809 | ||||||
chr5:140223148
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-20157G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223148 | ||||||
chr5:140223217
|
C | A | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(80): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-20088C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223217 | ||||||
chr5:140223309
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG02572.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-19996G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223309 | ||||||
chr5:140223423
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-19882T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223423 | ||||||
chr5:140223698
|
GCTTT | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0265 | 3 | HG01071.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.188-19605_188-1960 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140223698 | |||||
chr5:140223704
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0265 | 3 | HG01071.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.188-19601A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223704 | ||||||
chr5:140223925
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.188-19380A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223925 | ||||||
chr5:140223944
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-19361A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140223944 | ||||||
chr5:140224030
|
G | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-19275G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224030 | ||||||
chr5:140224217
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0239 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.188-19088G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224217 | ||||||
chr5:140224265
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0128others(8): Show | 13 | HG00438.hp1 NA18942.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-19040G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224265 | ||||||
chr5:140224289
|
G | A | 103 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(100): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.188-19016G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224289 | ||||||
chr5:140224934
|
T | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(246): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.188-18371T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224934 | ||||||
chr5:140224977
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.188-18328T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140224977 | ||||||
chr5:140225103
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.188-18202G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225103 | ||||||
chr5:140225118
|
G | A | 4 | a0001c0001t0002g0005a0001c0001t0002g0144a0001c0001t0002g0158others(1): Show | 5 | NA18988.hp2 NA19005.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-18187G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225118 | ||||||
chr5:140225275
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.188-18030C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225275 | ||||||
chr5:140225617
|
C | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-17688C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225617 | ||||||
chr5:140225632
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.188-17673T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225632 | ||||||
chr5:140225811
|
A | G | 24 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 24 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-17494A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225811 | ||||||
chr5:140225836
|
TTCTC | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0001t0001g0233others(1): Show | 4 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-17465_188-1746 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140225836 | |||||
chr5:140225932
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-17373G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140225932 | ||||||
chr5:140226148
|
GCCCAGCA others(5): Show |
G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-17155_188-1714 others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226148 | |||||
chr5:140226357
|
G | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-16948G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226357 | ||||||
chr5:140226470
|
A | AT | 100 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(97): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.188-16835_188-1683 others(5): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226470 | ||||||
chr5:140226476
|
T | TATATATT others(42): Show |
1 | a0001c0001t0001g0258 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.188-16812_188-1676 others(53): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226476 | |||||
chr5:140226483
|
T | A | 1 | a0001c0001t0003g0120 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.188-16822T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226483 | ||||||
chr5:140226485
|
A | T | 1 | a0001c0001t0003g0120 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.188-16820A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226485 | ||||||
chr5:140226494
|
TAA | T | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02071.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-16810_188-1680 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226494 | ||||||
chr5:140226497
|
T | TATATATA others(18): Show |
1 | a0001c0001t0003g0004 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.188-16801_188-1680 others(29): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226497 | |||||
chr5:140226501
|
TATAA | T | 20 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0111others(17): Show | 20 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.188-16800_188-1679 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226501 | |||||
chr5:140226503
|
TAA | T | 60 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(57): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.188-16800_188-1679 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226503 | |||||
chr5:140226505
|
A | T | 20 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(17): Show | 21 | HG00558.hp2 HG00621.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.188-16800A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226505 | ||||||
chr5:140226514
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188-16791T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226514 | ||||||
chr5:140226533
|
T | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16772T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226533 | ||||||
chr5:140226534
|
A | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-16771A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226534 | ||||||
chr5:140226552
|
A | C | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16753A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226552 | ||||||
chr5:140226555
|
T | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16750T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226555 | ||||||
chr5:140226559
|
A | T | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16746A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226559 | ||||||
chr5:140226564
|
A | T | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16741A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226564 | ||||||
chr5:140226582
|
A | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0301 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.188-16723A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226582 | ||||||
chr5:140226585
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-16720A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226585 | ||||||
chr5:140226586
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-16719T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226586 | ||||||
chr5:140226586
|
T | TTA | 45 | a0001c0001t0001g0014a0001c0001t0001g0048a0001c0001t0001g0058others(42): Show | 48 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.188-16694_188-1669 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATA | 43 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0185others(40): Show | 45 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.188-16696_188-1669 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATA | 13 | a0001c0001t0001g0234a0001c0001t0001g0241a0001c0001t0002g0005others(10): Show | 14 | HG00438.hp2 HG01884.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.188-16698_188-1669 others(10): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(1): Show |
10 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0002g0141others(7): Show | 10 | HG00323.hp2 HG01109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-16700_188-1669 others(12): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0304a0001c0001t0002g0114a0001c0001t0002g0129others(4): Show | 7 | HG00280.hp1 HG02056.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-16702_188-1669 others(14): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(5): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0084a0001c0001t0001g0189 | 3 | HG02572.hp1 NA18949.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.188-16704_188-1669 others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(7): Show |
12 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0056others(9): Show | 13 | HG01074.hp2 HG01257.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-16706_188-1669 others(18): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(9): Show |
15 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0066others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.188-16708_188-1669 others(20): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(11): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0047others(2): Show | 5 | HG00738.hp1 HG01496.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-16710_188-1669 others(22): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(13): Show |
15 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0028others(12): Show | 15 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.188-16712_188-1669 others(24): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(15): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0037others(5): Show | 8 | HG01361.hp1 HG02056.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-16714_188-1669 others(26): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0182 | 3 | HG01081.hp2 HG02976.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.188-16716_188-1669 others(28): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(21): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0044others(1): Show | 4 | NA18942.hp2 NA18975.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-16693_188-1669 others(32): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0039 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.188-16693_188-1669 others(34): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0038 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.188-16693_188-1669 others(36): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
TTA | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 19 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-16694_188-1669 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226586
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-16702_188-1669 others(14): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226586 | |||||
chr5:140226601
|
TATATATA others(5): Show |
T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02280.hp1 HG03486.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-16702_188-1669 others(16): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226601 | |||||
chr5:140226611
|
TAA | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0081 | 3 | NA18941.hp1 NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.188-16690_188-1668 others(6): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226611 | |||||
chr5:140226613
|
A | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(174): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.188-16692A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226613 | ||||||
chr5:140226614
|
A | T | 1 | a0001c0001t0002g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.188-16691A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226614 | ||||||
chr5:140226615
|
A | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0059 | 2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.188-16690A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226615 | ||||||
chr5:140226617
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-16688_188-1668 others(17): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226617 | ||||||
chr5:140226658
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-16647T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226658 | ||||||
chr5:140226684
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16621T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226684 | ||||||
chr5:140226714
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.188-16591C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226714 | ||||||
chr5:140226743
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-16562G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226743 | ||||||
chr5:140226766
|
C | CA | 11 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(8): Show | 11 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-16525dupA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140226766 | |||||
chr5:140226868
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.188-16437G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226868 | ||||||
chr5:140226998
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0219 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.188-16307G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140226998 | ||||||
chr5:140227109
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0194others(4): Show | 9 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-16196G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227109 | ||||||
chr5:140227133
|
G | A | 100 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(97): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.188-16172G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227133 | ||||||
chr5:140227334
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-15971T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227334 | ||||||
chr5:140227429
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188-15876G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227429 | ||||||
chr5:140227480
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.188-15825C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227480 | ||||||
chr5:140227702
|
C | T | 1 | a0001c0001t0003g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.188-15603C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227702 | ||||||
chr5:140227731
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.188-15574C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227731 | ||||||
chr5:140227908
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.188-15397A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227908 | ||||||
chr5:140227908
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.188-15397A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227908 | ||||||
chr5:140227935
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.188-15370T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227935 | ||||||
chr5:140227982
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01928.hp1 NA18961.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.188-15323C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140227982 | ||||||
chr5:140228278
|
C | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-15027C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140228278 | ||||||
chr5:140228335
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(78): Show | 82 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-14970G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140228335 | ||||||
chr5:140228570
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-14735T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140228570 | ||||||
chr5:140228768
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-14537T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140228768 | ||||||
chr5:140228801
|
C | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(78): Show | 82 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-14504C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140228801 | ||||||
chr5:140229037
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188-14268T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229037 | ||||||
chr5:140229110
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-14195G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229110 | ||||||
chr5:140229123
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.188-14182G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229123 | ||||||
chr5:140229138
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-14167A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229138 | ||||||
chr5:140229256
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(52): Show | 56 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.188-14049G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229256 | ||||||
chr5:140229292
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-14013T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229292 | ||||||
chr5:140229341
|
C | T | 83 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(80): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-13964C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229341 | ||||||
chr5:140229457
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.188-13848C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229457 | ||||||
chr5:140229607
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.188-13698G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229607 | ||||||
chr5:140229657
|
C | CGTTA | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-13645_188-1364 others(8): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140229657 | |||||
chr5:140229824
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-13481A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140229824 | ||||||
chr5:140230225
|
C | T | 11 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(8): Show | 11 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.188-13080C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140230225 | ||||||
chr5:140230366
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-12939T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140230366 | ||||||
chr5:140230367
|
T | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-12938T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140230367 | ||||||
chr5:140230672
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-12633T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140230672 | ||||||
chr5:140230997
|
GA | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186 | 3 | HG02572.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.188-12304delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140230997 | |||||
chr5:140231071
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.188-12234A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231071 | ||||||
chr5:140231426
|
A | T | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-11879A>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231426 | ||||||
chr5:140231438
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0265 | 3 | HG01071.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.188-11867G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231438 | ||||||
chr5:140231458
|
T | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-11847T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231458 | ||||||
chr5:140231605
|
A | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-11700A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231605 | ||||||
chr5:140231628
|
G | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-11677G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231628 | ||||||
chr5:140231695
|
G | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.188-11610G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231695 | ||||||
chr5:140231792
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188-11513C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231792 | ||||||
chr5:140231923
|
T | C | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-11382T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140231923 | ||||||
chr5:140232223
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.188-11082G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232223 | ||||||
chr5:140232259
|
T | C | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-11046T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232259 | ||||||
chr5:140232447
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-10858A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232447 | ||||||
chr5:140232507
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 86 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-10798A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232507 | ||||||
chr5:140232576
|
G | A | 2 | a0001c0001t0003g0134a0001c0001t0003g0138 | 2 | NA18941.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.188-10729G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232576 | ||||||
chr5:140232620
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.188-10685C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232620 | ||||||
chr5:140232766
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.188-10539G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140232766 | ||||||
chr5:140233269
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-10036A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233269 | ||||||
chr5:140233283
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0033 | 2 | NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.188-10022C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233283 | ||||||
chr5:140233518
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.188-9787G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233518 | ||||||
chr5:140233589
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02280.hp1 NA18906.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-9716G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233589 | ||||||
chr5:140233603
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-9702T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233603 | ||||||
chr5:140233805
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.188-9500C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233805 | ||||||
chr5:140233824
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188-9481T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233824 | ||||||
chr5:140233982
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-9323T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233982 | ||||||
chr5:140233986
|
A | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-9319A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140233986 | ||||||
chr5:140234062
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.188-9243C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234062 | ||||||
chr5:140234380
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0294a0001c0001t0001g0295 | 4 | HG02055.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-8925C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234380 | ||||||
chr5:140234626
|
T | C | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-8679T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234626 | ||||||
chr5:140234775
|
C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-8530C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234775 | ||||||
chr5:140234818
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.188-8487C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234818 | ||||||
chr5:140234853
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-8452C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140234853 | ||||||
chr5:140234969
|
AT | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 210 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.188-8319delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140234969 | |||||
chr5:140234969
|
ATT | A | 96 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(93): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.188-8320_188-8319d others(4): Show |
CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140234969 | |||||
chr5:140235210
|
T | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-8095T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140235210 | ||||||
chr5:140235408
|
CT | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(184): Show | 194 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.188-7882delT | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140235408 | |||||
chr5:140235502
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.188-7803T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140235502 | ||||||
chr5:140235507
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-7798G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140235507 | ||||||
chr5:140235867
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.188-7438G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140235867 | ||||||
chr5:140236076
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.188-7229G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236076 | ||||||
chr5:140236112
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-7193T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236112 | ||||||
chr5:140236221
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.188-7084A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236221 | ||||||
chr5:140236312
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.188-6993G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236312 | ||||||
chr5:140236314
|
G | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(78): Show | 82 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-6991G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236314 | ||||||
chr5:140236691
|
C | T | 1 | a0001c0001t0003g0004 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.188-6614C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236691 | ||||||
chr5:140236785
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.188-6520G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140236785 | ||||||
chr5:140237024
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-6281T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140237024 | ||||||
chr5:140237086
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-6219G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140237086 | ||||||
chr5:140237087
|
GA | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01496.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.188-6215delA | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140237087 | |||||
chr5:140237679
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.188-5626G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140237679 | ||||||
chr5:140237801
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-5504G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140237801 | ||||||
chr5:140237822
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-5483A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140237822 | ||||||
chr5:140238060
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-5245G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238060 | ||||||
chr5:140238069
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-5236T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238069 | ||||||
chr5:140238300
|
T | C | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.188-5005T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238300 | ||||||
chr5:140238306
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-4999T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238306 | ||||||
chr5:140238500
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 86 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-4805C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238500 | ||||||
chr5:140238557
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.188-4748T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238557 | ||||||
chr5:140238561
|
C | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-4744C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238561 | ||||||
chr5:140238578
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 86 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-4727G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238578 | ||||||
chr5:140238762
|
T | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0265 | 3 | HG01071.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.188-4543T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238762 | ||||||
chr5:140238947
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-4358T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238947 | ||||||
chr5:140238972
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.188-4333C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140238972 | ||||||
chr5:140239315
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.188-3990C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239315 | ||||||
chr5:140239368
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(78): Show | 82 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3937G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239368 | ||||||
chr5:140239623
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-3682T>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239623 | ||||||
chr5:140239780
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-3525T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239780 | ||||||
chr5:140239900
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.188-3405C>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239900 | ||||||
chr5:140239931
|
T | G | 1 | a0001c0001t0003g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.188-3374T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239931 | ||||||
chr5:140239934
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0297 | 2 | NA18986.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.188-3371C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140239934 | ||||||
chr5:140240024
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0128others(8): Show | 13 | HG00438.hp1 NA18942.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-3281C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240024 | ||||||
chr5:140240027
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0120others(2): Show | 5 | NA18951.hp1 NA18957.hp2 NA19077.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-3278T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240027 | ||||||
chr5:140240030
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.188-3275C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240030 | ||||||
chr5:140240139
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.188-3166G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240139 | ||||||
chr5:140240172
|
A | AC | 94 | a0001c0001t0001g0074a0001c0001t0001g0182a0001c0001t0001g0183others(91): Show | 99 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.188-3126dupC | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 140240172 | |||||
chr5:140240210
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0289 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.188-3095C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240210 | ||||||
chr5:140240369
|
C | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.188-2936C>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240369 | ||||||
chr5:140240541
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG00558.hp1 HG00673.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.188-2764C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240541 | ||||||
chr5:140240583
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.188-2722C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240583 | ||||||
chr5:140240859
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.188-2446C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240859 | ||||||
chr5:140240870
|
A | G | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-2435A>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140240870 | ||||||
chr5:140241208
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02280.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-2097C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241208 | ||||||
chr5:140241271
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.188-2034G>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241271 | ||||||
chr5:140241459
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.188-1846G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241459 | ||||||
chr5:140241765
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.188-1540G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241765 | ||||||
chr5:140241812
|
G | A | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-1493G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241812 | ||||||
chr5:140241985
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-1320G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140241985 | ||||||
chr5:140242034
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.188-1271G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242034 | ||||||
chr5:140242130
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.188-1175C>T | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242130 | ||||||
chr5:140242350
|
G | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-955G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242350 | ||||||
chr5:140242680
|
G | A | 102 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(99): Show | 107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.188-625G>A | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242680 | ||||||
chr5:140242687
|
T | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-618T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242687 | ||||||
chr5:140242760
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.188-545G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242760 | ||||||
chr5:140242791
|
T | G | 1 | a0001c0001t0001g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.188-514T>G | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242791 | ||||||
chr5:140242987
|
A | C | 101 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(98): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-318A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140242987 | ||||||
chr5:140243052
|
A | C | 1 | a0001c0001t0003g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.188-253A>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140243052 | ||||||
chr5:140243102
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.188-203G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140243102 | ||||||
chr5:140243105
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.188-200T>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140243105 | ||||||
chr5:140243119
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0265 | 3 | HG01071.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.188-186G>C | CYSTM1 | ENSG00000120306.11 | transcript | ENST00000261811.6 | protein_coding | 2/2 | chr5 | 140243119 |