Item | Value |
---|---|
geneid | 9474 |
ensemblid | ENSG00000057663.16 |
hgncid | 589 |
symbol | ATG5 |
name | autophagy related 5 |
refseq_nuc | NM_004849.4 |
refseq_prot | NP_004840.1 |
ensembl_nuc | ENST00000369076.8 |
ensembl_prot | ENSP00000358072.3 |
mane_status | MANE Select |
chr | chr6 |
start | 106184476 |
end | 106325760 |
strand | - |
ver | v1.2 |
region | chr6:106184476-106325760 |
region5000 | chr6:106179476-106330760 |
regionname0 | ATG5_chr6_106184476_106325760 |
regionname5000 | ATG5_chr6_106179476_106330760 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 275 | 350 | 70 | 56 | 172 | 14 | 36 | 139 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0002 | 0/0 | 275 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0003 | 0/0 | 275 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 828 | 344 | 66 | 56 | 172 | 12 | 36 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
c0002 | 0/0 | 828 | 6 | 0 | 0 | 6 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
c0003 | 0/0 | 828 | 4 | 4 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
c0004 | 0/0 | 828 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
c0005 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2358 | 328 | 61 | 53 | 172 | 8 | 32 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0002 | 0/0 | 2358 | 6 | 4 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0003 | 0/0 | 2358 | 5 | 0 | 0 | 5 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0004 | 0/0 | 2358 | 5 | 0 | 2 | 0 | 2 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0005 | 0/0 | 2354 | 4 | 4 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0006 | 0/0 | 2358 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0007 | 0/0 | 2358 | 2 | 0 | 0 | 0 | 0 | 2 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0008 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0009 | 0/0 | 2358 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0010 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0011 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
t0012 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 828 | 344 | 66 | 56 | 172 | 12 | 36 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
a0001c0003 | 0/0 | 828 | 4 | 4 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
a0001c0004 | 0/0 | 828 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
a0002c0002 | 0/0 | 828 | 6 | 0 | 0 | 6 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 | |
a0003c0005 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3185 | 322 | 61 | 53 | 166 | 8 | 32 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0003 | 0/0 | 3185 | 5 | 0 | 0 | 5 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0004 | 0/0 | 3185 | 5 | 0 | 2 | 0 | 2 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0005 | 0/0 | 3181 | 4 | 4 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0006 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0007 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 0 | 2 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0009 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0010 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0011 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0001t0012 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0003t0002 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0001c0004t0002 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0002c0002t0001 | 0/0 | 3185 | 6 | 0 | 0 | 6 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
a0003c0005t0008 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | copy fasta | chr6 | 106179476 | 106330760 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0009g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0004t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0003c0005t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
a0003c0005t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0097 | EUR | FIN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0284 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0348 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0002 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01516 | hp2 | a0001 | c0004 | t0002 | g0015 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01517 | hp1 | a0001 | c0004 | t0002 | g0016 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0002 | EUR | IBS | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02055 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02145 | hp1 | a0003 | c0005 | t0008 | g0068 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02257 | hp2 | a0003 | c0005 | t0008 | g0067 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0334 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0335 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0205 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0212 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0330 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | LWK | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | LWK | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19076 | hp2 | a0001 | c0001 | t0011 | g0248 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0346 | EUR | TSI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | GIH | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0259 | REF | REF | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0285 | REF | REF | ATG5_chr6_106179476_106330760 | ATG5 | chr6 | 106179476 | 106330760 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:106279754 | T | C | 1 | a0003 | 2 | HG02145.hp1 HG02257.hp2 |
missense_variant | MODERATE | c.385A>G | p.Met129Val | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/8 | 678/3185 | 385/828 | 129/275 | chr6 | 106279754 | ||
chr6:106308407 | T | C | 1 | a0002 | 6 | HG00558.hp2 NA18944.hp2 NA18965.hp2 others(3): Show |
missense_variant | MODERATE | c.193A>G | p.Ile65Val | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/8 | 486/3185 | 193/828 | 65/275 | chr6 | 106308407 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:106279695 | T | C | 2 | a0001c0003a0001c0004 | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
synonymous_variant | LOW | c.444A>G | p.Lys148Lys | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/8 | 737/3185 | 444/828 | 148/275 | chr6 | 106279695 | ||
chr6:106316143 | T | C | 1 | a0001c0003 | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.66A>G | p.Leu22Leu | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/8 | 359/3185 | 66/828 | 22/275 | chr6 | 106316143 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:106184787 | C | G | 1 | a0003c0005t0008 | 2 | HG02145.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1753G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 1753 | chr6 | 106184787 | |||||
chr6:106184854 | T | C | 1 | a0001c0001t0003 | 5 | NA18940.hp1 NA18942.hp2 NA18945.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1686A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 1686 | chr6 | 106184854 | |||||
chr6:106185019 | G | A | 2 | a0001c0003t0002a0001c0004t0002 | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1521C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 1521 | chr6 | 106185019 | |||||
chr6:106185478 | C | A | 1 | a0001c0001t0004 | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1062G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 1062 | chr6 | 106185478 | |||||
chr6:106185533 | T | A | 1 | a0001c0001t0009 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1007A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 1007 | chr6 | 106185533 | |||||
chr6:106185758 | T | C | 1 | a0001c0001t0010 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 782 | chr6 | 106185758 | |||||
chr6:106185831 | C | T | 1 | a0001c0001t0005 | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*709G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 709 | chr6 | 106185831 | |||||
chr6:106185871 | CTGTA | C | 1 | a0001c0001t0005 | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*668delTACA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 665 | chr6 | 106185871 | |||||
chr6:106185877 | G | A | 1 | a0001c0001t0011 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 663 | chr6 | 106185877 | |||||
chr6:106186500 | C | T | 1 | a0001c0001t0007 | 2 | HG03239.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*40G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 8/8 | 40 | chr6 | 106186500 | |||||
chr6:106316245 | T | C | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/8 | 37 | chr6 | 106316245 | |||||
chr6:106325620 | C | T | 1 | a0001c0001t0006 | 2 | HG01515.hp2 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-153G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/8 | 9412 | chr6 | 106325620 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:106186694 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-18G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106186694 | ||||||
chr6:106186782 | T | C | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | NA18961.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.692-106A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106186782 | ||||||
chr6:106186966 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.692-290A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106186966 | ||||||
chr6:106186978 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.692-302G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106186978 | ||||||
chr6:106187065 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.692-389C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187065 | ||||||
chr6:106187086 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.692-410A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187086 | ||||||
chr6:106187113 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-437T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187113 | ||||||
chr6:106187568 | T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.692-892A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187568 | ||||||
chr6:106187857 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-1181C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187857 | ||||||
chr6:106187902 | CT | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-1227delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106187902 | ||||||
chr6:106188227 | G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01175.hp1 HG01346.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.692-1551C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106188227 | ||||||
chr6:106188421 | C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.692-1745G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106188421 | ||||||
chr6:106188584 | G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0103others(1): Show | 4 | HG01175.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-1908C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106188584 | ||||||
chr6:106188596 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.692-1920G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106188596 | ||||||
chr6:106188764 | C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.692-2088G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106188764 | ||||||
chr6:106189027 | T | C | 21 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.692-2351A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189027 | ||||||
chr6:106189173 | C | T | 6 | a0001c0001t0001g0249a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.692-2497G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189173 | ||||||
chr6:106189342 | T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(53): Show | 60 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.692-2666A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189342 | ||||||
chr6:106189646 | T | TA | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.692-2971dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189646 | ||||||
chr6:106189646 | T | TAA | 44 | a0001c0001t0001g0020a0001c0001t0001g0071a0001c0001t0001g0075others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-2972_692-2971d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189646 | ||||||
chr6:106189700 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-3024G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189700 | ||||||
chr6:106189918 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.692-3242A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106189918 | ||||||
chr6:106190115 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.692-3439A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106190115 | ||||||
chr6:106190124 | T | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.692-3448A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106190124 | ||||||
chr6:106190234 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.692-3558G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106190234 | ||||||
chr6:106190260 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.692-3584C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106190260 | ||||||
chr6:106191027 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.692-4351G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191027 | ||||||
chr6:106191436 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.692-4760C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191436 | ||||||
chr6:106191544 | A | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.692-4868T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191544 | ||||||
chr6:106191564 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.692-4888A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191564 | ||||||
chr6:106191646 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-4970A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191646 | ||||||
chr6:106191750 | C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.692-5074G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191750 | ||||||
chr6:106191919 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.692-5243A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191919 | ||||||
chr6:106191949 | C | T | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.692-5273G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191949 | ||||||
chr6:106191973 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.692-5297A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106191973 | ||||||
chr6:106192178 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.692-5502C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192178 | ||||||
chr6:106192228 | T | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0299a0001c0001t0001g0316others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.692-5552A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192228 | ||||||
chr6:106192229 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.692-5553T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192229 | ||||||
chr6:106192397 | G | A | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.692-5721C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192397 | ||||||
chr6:106192663 | C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0176 | 3 | HG00642.hp1 HG02258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.692-5987G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192663 | ||||||
chr6:106192977 | G | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0271 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.692-6301C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106192977 | ||||||
chr6:106193217 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.692-6541G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193217 | ||||||
chr6:106193298 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.692-6622A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193298 | ||||||
chr6:106193327 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-6651T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193327 | ||||||
chr6:106193755 | C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(92): Show | 99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.692-7079G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193755 | ||||||
chr6:106193833 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.692-7157G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193833 | ||||||
chr6:106193861 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.692-7185G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106193861 | ||||||
chr6:106194217 | A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(229): Show | 239 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.692-7541T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194217 | ||||||
chr6:106194333 | C | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.691+7639G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194333 | ||||||
chr6:106194345 | A | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.691+7627T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194345 | ||||||
chr6:106194429 | C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(229): Show | 239 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.691+7543G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194429 | ||||||
chr6:106194528 | CTTTTCT | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.691+7438_691+7443d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194528 | ||||||
chr6:106194545 | C | CT | 25 | a0001c0001t0001g0069a0001c0001t0001g0295a0001c0001t0001g0297others(22): Show | 25 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.691+7426dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194545 | ||||||
chr6:106194663 | A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.691+7309T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194663 | ||||||
chr6:106194772 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.691+7200C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194772 | ||||||
chr6:106194812 | C | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(6): Show | 10 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.691+7160G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106194812 | ||||||
chr6:106195013 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.691+6959G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195013 | ||||||
chr6:106195186 | T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(97): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.691+6786A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195186 | ||||||
chr6:106195260 | C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+6712G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195260 | ||||||
chr6:106195333 | T | C | 14 | a0001c0001t0001g0107a0001c0001t0001g0153a0001c0001t0001g0193others(11): Show | 14 | HG02132.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.691+6639A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195333 | ||||||
chr6:106195346 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.691+6626G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195346 | ||||||
chr6:106195365 | A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 237 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.691+6607T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195365 | ||||||
chr6:106195448 | C | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00140.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.691+6524G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195448 | ||||||
chr6:106195482 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.691+6490T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195482 | ||||||
chr6:106195808 | T | TA | 38 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0056others(35): Show | 38 | HG00609.hp2 HG00673.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.691+6163dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195808 | ||||||
chr6:106195808 | T | TAA | 7 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0295others(4): Show | 7 | HG00099.hp2 NA18961.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.691+6162_691+6163d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195808 | ||||||
chr6:106195808 | TA | T | 51 | a0001c0001t0001g0027a0001c0001t0001g0071a0001c0001t0001g0073others(48): Show | 51 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.691+6163delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195808 | ||||||
chr6:106195808 | TAA | T | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 72 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.691+6162_691+6163d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106195808 | ||||||
chr6:106196169 | G | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.691+5803C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196169 | ||||||
chr6:106196223 | T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02135.hp1 HG02165.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+5749A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196223 | ||||||
chr6:106196228 | A | G | 12 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01175.hp1 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.691+5744T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196228 | ||||||
chr6:106196722 | CA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.691+5249delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196722 | ||||||
chr6:106196809 | TTCCCACT others(23): Show |
T | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.691+5133_691+5162d others(32): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196809 | ||||||
chr6:106196841 | C | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.691+5131G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196841 | ||||||
chr6:106196845 | C | T | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.691+5127G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196845 | ||||||
chr6:106196955 | GTTAAC | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+5012_691+5016d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196955 | ||||||
chr6:106196966 | T | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.691+5006A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106196966 | ||||||
chr6:106197004 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.691+4968G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197004 | ||||||
chr6:106197023 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.691+4949C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197023 | ||||||
chr6:106197031 | A | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.691+4941T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197031 | ||||||
chr6:106197059 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.691+4913A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197059 | ||||||
chr6:106197078 | C | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.691+4894G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197078 | ||||||
chr6:106197099 | A | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.691+4873T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197099 | ||||||
chr6:106197168 | T | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG00609.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.691+4804A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197168 | ||||||
chr6:106197333 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.691+4639G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197333 | ||||||
chr6:106197418 | T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099others(2): Show | 7 | NA18962.hp1 NA18964.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.691+4554A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197418 | ||||||
chr6:106197429 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.691+4543T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197429 | ||||||
chr6:106197528 | T | TG | 55 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0025others(52): Show | 55 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.691+4443dupC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197528 | ||||||
chr6:106197961 | G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.691+4011C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106197961 | ||||||
chr6:106198003 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.691+3969C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198003 | ||||||
chr6:106198107 | A | AAC | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.691+3863_691+3864d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198107 | ||||||
chr6:106198221 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.691+3751A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198221 | ||||||
chr6:106198228 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.691+3744G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198228 | ||||||
chr6:106198368 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.691+3604A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198368 | ||||||
chr6:106198528 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.691+3444C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198528 | ||||||
chr6:106198768 | CCTGTCTG | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3197_691+3203d others(9): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198768 | ||||||
chr6:106198776 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3196C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198776 | ||||||
chr6:106198777 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3195C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198777 | ||||||
chr6:106198777 | G | GA | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(174): Show | 184 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.691+3194dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198777 | ||||||
chr6:106198939 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3033T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198939 | ||||||
chr6:106198957 | A | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+3015T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198957 | ||||||
chr6:106198975 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+2997T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106198975 | ||||||
chr6:106199362 | C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18978.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.691+2610G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199362 | ||||||
chr6:106199444 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.691+2528C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199444 | ||||||
chr6:106199787 | G | A | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.691+2185C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199787 | ||||||
chr6:106199813 | T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.691+2159A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199813 | ||||||
chr6:106199876 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.691+2096A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199876 | ||||||
chr6:106199943 | T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0113a0001c0001t0001g0124others(5): Show | 9 | HG00099.hp1 HG01074.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.691+2029A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106199943 | ||||||
chr6:106200185 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.691+1787A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200185 | ||||||
chr6:106200477 | A | AT | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 67 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.691+1494dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200477 | ||||||
chr6:106200697 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+1275C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200697 | ||||||
chr6:106200726 | C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 50 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.691+1246G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200726 | ||||||
chr6:106200801 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.691+1171T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200801 | ||||||
chr6:106200845 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.691+1127G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200845 | ||||||
chr6:106200883 | T | TAC | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 77 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.691+1087_691+1088d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200883 | ||||||
chr6:106200889 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.691+1083G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200889 | ||||||
chr6:106200975 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.691+997G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200975 | ||||||
chr6:106200979 | T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.691+993A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106200979 | ||||||
chr6:106201002 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.691+970G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201002 | ||||||
chr6:106201053 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.691+919C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201053 | ||||||
chr6:106201246 | A | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.691+726T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201246 | ||||||
chr6:106201275 | A | ATG | 14 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(11): Show | 15 | HG00323.hp1 HG00735.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.691+695_691+696dup others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | A | ATGTG | 35 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0101others(32): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.691+693_691+696dup others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | A | ATGTGTG | 11 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0178others(8): Show | 11 | HG01346.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.691+691_691+696dup others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | A | ATGTGTGT others(1): Show |
4 | a0001c0003t0002g0011a0001c0003t0002g0014a0001c0004t0002g0015others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+689_691+696dup others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.691+683_691+696dup others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | A | G | 1 | a0001c0003t0002g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691+697T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | ATG | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(137): Show | 147 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.691+695_691+696del others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201275 | ATGTG | A | 43 | a0001c0001t0001g0069a0001c0001t0001g0109a0001c0001t0001g0247others(40): Show | 43 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.691+693_691+696del others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201275 | ||||||
chr6:106201289 | G | A | 1 | a0002c0002t0001g0051 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691+683C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201289 | ||||||
chr6:106201585 | T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0309 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.691+387A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201585 | ||||||
chr6:106201771 | G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.691+201C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201771 | ||||||
chr6:106201817 | T | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.691+155A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 7/7 | chr6 | 106201817 | ||||||
chr6:106202605 | A | T | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.574-516T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106202605 | ||||||
chr6:106202694 | C | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.574-605G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106202694 | ||||||
chr6:106202722 | C | T | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-633G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106202722 | ||||||
chr6:106202947 | G | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.574-858C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106202947 | ||||||
chr6:106202977 | A | C | 1 | a0001c0001t0001g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.574-888T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106202977 | ||||||
chr6:106203131 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1042G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106203131 | ||||||
chr6:106203513 | G | A | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.574-1424C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106203513 | ||||||
chr6:106203737 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.574-1648A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106203737 | ||||||
chr6:106203876 | T | A | 2 | a0001c0001t0007g0205a0001c0001t0007g0212 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.574-1787A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106203876 | ||||||
chr6:106204019 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.574-1930G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204019 | ||||||
chr6:106204101 | T | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-2012A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204101 | ||||||
chr6:106204168 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.574-2079G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204168 | ||||||
chr6:106204502 | T | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-2413A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204502 | ||||||
chr6:106204526 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-2437G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204526 | ||||||
chr6:106204546 | C | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG00738.hp1 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-2457G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204546 | ||||||
chr6:106204547 | G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.574-2458C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204547 | ||||||
chr6:106204567 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-2478G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204567 | ||||||
chr6:106204780 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.574-2691C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204780 | ||||||
chr6:106204905 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.574-2816C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204905 | ||||||
chr6:106204935 | G | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | NA18950.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.574-2846C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106204935 | ||||||
chr6:106205263 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.574-3174T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205263 | ||||||
chr6:106205454 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-3365C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205454 | ||||||
chr6:106205486 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.574-3397T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205486 | ||||||
chr6:106205535 | A | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.574-3446T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205535 | ||||||
chr6:106205694 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-3605A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205694 | ||||||
chr6:106205718 | G | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0044others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-3629C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205718 | ||||||
chr6:106205996 | G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG01175.hp1 HG01346.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-3907C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106205996 | ||||||
chr6:106206219 | G | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.574-4130C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206219 | ||||||
chr6:106206276 | C | T | 12 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01175.hp1 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-4187G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206276 | ||||||
chr6:106206338 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-4249G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206338 | ||||||
chr6:106206418 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.574-4329G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206418 | ||||||
chr6:106206648 | CA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 190 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.574-4560delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206648 | ||||||
chr6:106206668 | A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(53): Show | 60 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.574-4579T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206668 | ||||||
chr6:106206779 | A | G | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.574-4690T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106206779 | ||||||
chr6:106207053 | A | C | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.574-4964T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207053 | ||||||
chr6:106207324 | C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | NA18612.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.574-5235G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207324 | ||||||
chr6:106207504 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.574-5415A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207504 | ||||||
chr6:106207531 | T | TC | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-5443dupG | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207531 | ||||||
chr6:106207533 | T | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-5444A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207533 | ||||||
chr6:106207536 | T | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-5447A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207536 | ||||||
chr6:106207543 | A | G | 21 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.574-5454T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207543 | ||||||
chr6:106207547 | G | T | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-5458C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207547 | ||||||
chr6:106207606 | A | G | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.574-5517T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207606 | ||||||
chr6:106207742 | T | C | 21 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.574-5653A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207742 | ||||||
chr6:106207811 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.574-5722G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207811 | ||||||
chr6:106207848 | C | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0331 | 2 | NA18942.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.574-5759G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207848 | ||||||
chr6:106207860 | G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(8): Show | 11 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-5771C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207860 | ||||||
chr6:106207922 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.574-5833A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106207922 | ||||||
chr6:106208029 | T | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-5940A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208029 | ||||||
chr6:106208140 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.574-6051G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208140 | ||||||
chr6:106208203 | T | TACATATG others(23): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0123a0001c0001t0001g0132 | 3 | HG03209.hp2 HG04228.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.574-6144_574-6115d others(32): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208203 | ||||||
chr6:106208224 | C | CTGTGTAA others(23): Show |
19 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(16): Show | 19 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-6136_574-6135i others(32): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208224 | ||||||
chr6:106208254 | C | A | 41 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(38): Show | 41 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.574-6165G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208254 | ||||||
chr6:106208254 | C | CTGTGTAA others(23): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG02698.hp1 NA18977.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.574-6166_574-6165i others(32): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208254 | ||||||
chr6:106208274 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.574-6185T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208274 | ||||||
chr6:106208550 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-6461T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208550 | ||||||
chr6:106208689 | C | G | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.574-6600G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208689 | ||||||
chr6:106208775 | C | T | 1 | a0001c0001t0007g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.574-6686G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208775 | ||||||
chr6:106208887 | C | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0271 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.574-6798G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208887 | ||||||
chr6:106208900 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-6811A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208900 | ||||||
chr6:106208958 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.574-6869C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208958 | ||||||
chr6:106208959 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.574-6870G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208959 | ||||||
chr6:106208983 | C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.574-6894G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106208983 | ||||||
chr6:106209021 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.574-6932A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209021 | ||||||
chr6:106209276 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.574-7187G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209276 | ||||||
chr6:106209368 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.574-7279C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209368 | ||||||
chr6:106209387 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.574-7298A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209387 | ||||||
chr6:106209469 | G | C | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.574-7380C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209469 | ||||||
chr6:106209484 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.574-7395A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209484 | ||||||
chr6:106209643 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.574-7554A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209643 | ||||||
chr6:106209742 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-7653C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209742 | ||||||
chr6:106209751 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.574-7662G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209751 | ||||||
chr6:106209783 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.574-7694C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209783 | ||||||
chr6:106209851 | A | T | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-7762T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209851 | ||||||
chr6:106209954 | T | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.574-7865A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209954 | ||||||
chr6:106209972 | A | G | 1 | a0001c0001t0003g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.574-7883T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106209972 | ||||||
chr6:106210255 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.574-8166C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106210255 | ||||||
chr6:106210656 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.574-8567T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106210656 | ||||||
chr6:106210660 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.574-8571A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106210660 | ||||||
chr6:106210759 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.574-8670T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106210759 | ||||||
chr6:106211222 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.574-9133G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211222 | ||||||
chr6:106211365 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-9276C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211365 | ||||||
chr6:106211529 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.574-9440G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211529 | ||||||
chr6:106211566 | C | T | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574-9477G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211566 | ||||||
chr6:106211875 | A | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-9786T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211875 | ||||||
chr6:106211893 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.574-9804C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211893 | ||||||
chr6:106211981 | G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.574-9892C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106211981 | ||||||
chr6:106212171 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-10082C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106212171 | ||||||
chr6:106212411 | C | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099others(3): Show | 8 | NA18962.hp1 NA18964.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-10322G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106212411 | ||||||
chr6:106212522 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.574-10433G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106212522 | ||||||
chr6:106212865 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.574-10776G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106212865 | ||||||
chr6:106212885 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.574-10796T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106212885 | ||||||
chr6:106213026 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.574-10937G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106213026 | ||||||
chr6:106213655 | T | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.574-11566A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106213655 | ||||||
chr6:106213749 | C | T | 4 | a0001c0001t0001g0247a0001c0001t0001g0300a0001c0001t0001g0305others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-11660G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106213749 | ||||||
chr6:106213801 | T | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-11712A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106213801 | ||||||
chr6:106213881 | T | C | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.574-11792A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106213881 | ||||||
chr6:106214062 | G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0286 | 2 | HG00558.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.574-11973C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214062 | ||||||
chr6:106214311 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.574-12222C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214311 | ||||||
chr6:106214395 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.574-12306A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214395 | ||||||
chr6:106214397 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.574-12308T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214397 | ||||||
chr6:106214476 | T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-12387A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214476 | ||||||
chr6:106214617 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.574-12528A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214617 | ||||||
chr6:106214687 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-12598A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214687 | ||||||
chr6:106214696 | A | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-12607T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214696 | ||||||
chr6:106214703 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.574-12614C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214703 | ||||||
chr6:106214801 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-12712C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214801 | ||||||
chr6:106214866 | C | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.574-12777G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214866 | ||||||
chr6:106214885 | C | A | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.574-12796G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214885 | ||||||
chr6:106214941 | T | A | 1 | a0001c0001t0001g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.574-12852A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106214941 | ||||||
chr6:106215067 | G | C | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.574-12978C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215067 | ||||||
chr6:106215262 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.574-13173G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215262 | ||||||
chr6:106215302 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.574-13213T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215302 | ||||||
chr6:106215387 | T | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | NA18946.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-13298A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215387 | ||||||
chr6:106215398 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.574-13309T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215398 | ||||||
chr6:106215538 | GATAA | G | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-13453_574-1345 others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215538 | ||||||
chr6:106215568 | G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.574-13479C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215568 | ||||||
chr6:106215879 | A | T | 2 | a0001c0004t0002g0015a0001c0004t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.574-13790T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215879 | ||||||
chr6:106215995 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.574-13906T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106215995 | ||||||
chr6:106216104 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-14015C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216104 | ||||||
chr6:106216211 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.574-14122A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216211 | ||||||
chr6:106216225 | AACCCAGC others(6): Show |
A | 2 | a0001c0003t0002g0012a0001c0003t0002g0014 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.574-14149_574-1413 others(17): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216225 | ||||||
chr6:106216395 | A | G | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-14306T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216395 | ||||||
chr6:106216581 | G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259 | 3 | HG00639.hp1 HG01943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.574-14492C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216581 | ||||||
chr6:106216961 | T | TAA | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-14874_574-1487 others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216961 | ||||||
chr6:106216961 | TA | T | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.574-14873delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106216961 | ||||||
chr6:106217160 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.574-15071T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217160 | ||||||
chr6:106217248 | G | A | 6 | a0001c0001t0001g0237a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-15159C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217248 | ||||||
chr6:106217648 | T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(53): Show | 60 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.574-15559A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217648 | ||||||
chr6:106217685 | A | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 50 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.574-15596T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217685 | ||||||
chr6:106217697 | C | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-15608G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217697 | ||||||
chr6:106217710 | T | C | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-15621A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217710 | ||||||
chr6:106217827 | G | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 57 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.574-15738C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217827 | ||||||
chr6:106217866 | C | CA | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-15778dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217866 | ||||||
chr6:106217877 | C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.574-15788G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217877 | ||||||
chr6:106217959 | T | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.574-15870A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106217959 | ||||||
chr6:106218112 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.574-16023A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218112 | ||||||
chr6:106218134 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.574-16045T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218134 | ||||||
chr6:106218267 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-16178T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218267 | ||||||
chr6:106218342 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-16253C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218342 | ||||||
chr6:106218699 | A | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02040.hp2 NA18952.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-16610T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218699 | ||||||
chr6:106218811 | A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0167others(1): Show | 4 | NA18939.hp1 NA19011.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-16722T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106218811 | ||||||
chr6:106219003 | GA | G | 39 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(36): Show | 39 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.574-16915delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219003 | ||||||
chr6:106219021 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.574-16932T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219021 | ||||||
chr6:106219394 | C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 238 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.574-17305G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219394 | ||||||
chr6:106219468 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.574-17379A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219468 | ||||||
chr6:106219536 | T | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02040.hp2 NA18952.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-17447A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219536 | ||||||
chr6:106219536 | T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.574-17447A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219536 | ||||||
chr6:106219629 | C | T | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-17540G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219629 | ||||||
chr6:106219660 | T | G | 21 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.574-17571A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219660 | ||||||
chr6:106219931 | T | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 24 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-17842A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106219931 | ||||||
chr6:106220059 | T | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-17970A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220059 | ||||||
chr6:106220116 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-18027G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220116 | ||||||
chr6:106220119 | C | T | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.574-18030G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220119 | ||||||
chr6:106220305 | C | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-18216G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220305 | ||||||
chr6:106220352 | G | C | 1 | a0002c0002t0001g0052 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.574-18263C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220352 | ||||||
chr6:106220430 | AG | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.574-18342delC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220430 | ||||||
chr6:106220617 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.574-18528T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220617 | ||||||
chr6:106220832 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-18743G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220832 | ||||||
chr6:106220964 | T | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.574-18875A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106220964 | ||||||
chr6:106221264 | C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(51): Show | 58 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.574-19175G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221264 | ||||||
chr6:106221322 | T | C | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-19233A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221322 | ||||||
chr6:106221414 | G | A | 12 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.574-19325C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221414 | ||||||
chr6:106221450 | C | G | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.574-19361G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221450 | ||||||
chr6:106221461 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.574-19372C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221461 | ||||||
chr6:106221462 | G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0113a0001c0001t0001g0124others(7): Show | 11 | HG00099.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-19373C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221462 | ||||||
chr6:106221481 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-19392A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221481 | ||||||
chr6:106221503 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.574-19414A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221503 | ||||||
chr6:106221559 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-19470C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221559 | ||||||
chr6:106221584 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-19495C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221584 | ||||||
chr6:106221685 | C | CA | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.574-19597dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221685 | ||||||
chr6:106221685 | C | CAAA | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099others(3): Show | 8 | NA18962.hp1 NA18964.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-19599_574-1959 others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221685 | ||||||
chr6:106221711 | G | GA | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(59): Show | 66 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.574-19623dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221711 | ||||||
chr6:106221711 | G | GAA | 37 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.574-19624_574-1962 others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221711 | ||||||
chr6:106221830 | T | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-19741A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221830 | ||||||
chr6:106221996 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.574-19907T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106221996 | ||||||
chr6:106222017 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.574-19928C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222017 | ||||||
chr6:106222035 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.574-19946C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222035 | ||||||
chr6:106222212 | G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(53): Show | 60 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.574-20123C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222212 | ||||||
chr6:106222214 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-20125C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222214 | ||||||
chr6:106222459 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574-20370T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222459 | ||||||
chr6:106222499 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-20410G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222499 | ||||||
chr6:106222508 | C | T | 10 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(7): Show | 10 | HG00558.hp1 HG00621.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.574-20419G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222508 | ||||||
chr6:106222973 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-20884A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222973 | ||||||
chr6:106222979 | A | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.574-20890T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106222979 | ||||||
chr6:106223164 | T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.574-21075A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223164 | ||||||
chr6:106223324 | T | G | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.574-21235A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223324 | ||||||
chr6:106223353 | G | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-21264C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223353 | ||||||
chr6:106223442 | C | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0224 | 2 | HG00621.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.574-21353G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223442 | ||||||
chr6:106223512 | T | C | 1 | a0001c0003t0002g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.574-21423A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223512 | ||||||
chr6:106223516 | C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035others(2): Show | 6 | HG00140.hp1 NA18954.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-21427G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223516 | ||||||
chr6:106223694 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574-21605A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223694 | ||||||
chr6:106223716 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.574-21627A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223716 | ||||||
chr6:106223737 | C | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0176 | 3 | HG00642.hp1 HG02258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.574-21648G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223737 | ||||||
chr6:106223853 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.574-21764A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106223853 | ||||||
chr6:106224048 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.574-21959C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224048 | ||||||
chr6:106224139 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.574-22050G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224139 | ||||||
chr6:106224546 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.574-22457C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224546 | ||||||
chr6:106224569 | A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.574-22480T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224569 | ||||||
chr6:106224701 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.574-22612G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224701 | ||||||
chr6:106224796 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-22707C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224796 | ||||||
chr6:106224838 | A | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-22749T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224838 | ||||||
chr6:106224875 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.574-22786G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224875 | ||||||
chr6:106224996 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.574-22907G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106224996 | ||||||
chr6:106225077 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.574-22988A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225077 | ||||||
chr6:106225097 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.574-23008A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225097 | ||||||
chr6:106225430 | A | AACATGAG others(24): Show |
1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.573+22719_573+2272 others(35): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225430 | ||||||
chr6:106225431 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.573+22719A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225431 | ||||||
chr6:106225433 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.573+22717G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225433 | ||||||
chr6:106225722 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573+22428A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225722 | ||||||
chr6:106225923 | A | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+22227T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106225923 | ||||||
chr6:106226032 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+22118G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226032 | ||||||
chr6:106226128 | A | G | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.573+22022T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226128 | ||||||
chr6:106226174 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.573+21976T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226174 | ||||||
chr6:106226436 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+21714A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226436 | ||||||
chr6:106226588 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.573+21562C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226588 | ||||||
chr6:106226756 | A | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+21394T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226756 | ||||||
chr6:106226830 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+21320G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226830 | ||||||
chr6:106226975 | G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(225): Show | 235 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.573+21175C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106226975 | ||||||
chr6:106227064 | C | T | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.573+21086G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227064 | ||||||
chr6:106227181 | A | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.573+20969T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227181 | ||||||
chr6:106227572 | G | GGA | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.573+20576_573+2057 others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227572 | ||||||
chr6:106227636 | A | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0149 | 3 | NA18944.hp1 NA18948.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.573+20514T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227636 | ||||||
chr6:106227760 | T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+20390A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227760 | ||||||
chr6:106227847 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.573+20303T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227847 | ||||||
chr6:106227891 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.573+20259A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227891 | ||||||
chr6:106227944 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+20206A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106227944 | ||||||
chr6:106228118 | T | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01175.hp1 HG01346.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+20032A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228118 | ||||||
chr6:106228120 | A | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+20030T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228120 | ||||||
chr6:106228206 | C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18950.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.573+19944G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228206 | ||||||
chr6:106228260 | A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 246 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.573+19890T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228260 | ||||||
chr6:106228323 | G | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+19827C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228323 | ||||||
chr6:106228362 | C | T | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.573+19788G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228362 | ||||||
chr6:106228572 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.573+19578A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228572 | ||||||
chr6:106228595 | C | T | 19 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(16): Show | 19 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.573+19555G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228595 | ||||||
chr6:106228611 | G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01255.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.573+19539C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228611 | ||||||
chr6:106228685 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.573+19465G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228685 | ||||||
chr6:106228727 | G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 238 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.573+19423C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106228727 | ||||||
chr6:106229113 | A | T | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.573+19037T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229113 | ||||||
chr6:106229241 | C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.573+18909G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229241 | ||||||
chr6:106229347 | T | G | 1 | a0001c0003t0002g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.573+18803A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229347 | ||||||
chr6:106229472 | C | T | 3 | a0001c0001t0005g0333a0001c0001t0005g0335a0001c0001t0005g0336 | 3 | HG02970.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.573+18678G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229472 | ||||||
chr6:106229524 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+18626C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229524 | ||||||
chr6:106229559 | T | TA | 20 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(17): Show | 22 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.573+18590dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229559 | ||||||
chr6:106229569 | CAG | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+18579_573+1858 others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229569 | ||||||
chr6:106229576 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+18574G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229576 | ||||||
chr6:106229823 | A | G | 2 | a0001c0003t0002g0012a0001c0003t0002g0014 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.573+18327T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106229823 | ||||||
chr6:106230229 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.573+17921C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230229 | ||||||
chr6:106230296 | G | A | 2 | a0001c0003t0002g0012a0001c0003t0002g0014 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.573+17854C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230296 | ||||||
chr6:106230381 | C | T | 2 | a0001c0003t0002g0012a0001c0003t0002g0014 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.573+17769G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230381 | ||||||
chr6:106230513 | G | A | 1 | a0002c0002t0001g0052 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.573+17637C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230513 | ||||||
chr6:106230628 | T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(95): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.573+17522A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230628 | ||||||
chr6:106230692 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.573+17458G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230692 | ||||||
chr6:106230896 | C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(95): Show | 102 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.573+17254G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230896 | ||||||
chr6:106230937 | G | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 63 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.573+17213C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106230937 | ||||||
chr6:106231046 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+17104C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231046 | ||||||
chr6:106231090 | A | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+17060T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231090 | ||||||
chr6:106231157 | C | T | 5 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01891.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+16993G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231157 | ||||||
chr6:106231426 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+16724C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231426 | ||||||
chr6:106231545 | T | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+16605A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231545 | ||||||
chr6:106231581 | AG | A | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.573+16568delC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231581 | ||||||
chr6:106231651 | A | C | 42 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(39): Show | 42 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.573+16499T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231651 | ||||||
chr6:106231800 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.573+16350A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231800 | ||||||
chr6:106231813 | G | A | 1 | a0001c0001t0004g0346 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.573+16337C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231813 | ||||||
chr6:106231850 | C | T | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573+16300G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231850 | ||||||
chr6:106231881 | G | A | 4 | a0001c0001t0003g0108a0001c0001t0003g0191a0001c0001t0003g0192others(1): Show | 4 | NA18940.hp1 NA18942.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+16269C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231881 | ||||||
chr6:106231935 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.573+16215C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106231935 | ||||||
chr6:106232032 | C | T | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+16118G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232032 | ||||||
chr6:106232263 | G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 246 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.573+15887C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232263 | ||||||
chr6:106232749 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.573+15401T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232749 | ||||||
chr6:106232866 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.573+15284A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232866 | ||||||
chr6:106232881 | A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0123 | 4 | HG02809.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+15269T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232881 | ||||||
chr6:106232956 | G | A | 2 | a0002c0002t0001g0054a0002c0002t0001g0058 | 2 | NA18944.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.573+15194C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106232956 | ||||||
chr6:106233068 | G | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+15082C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233068 | ||||||
chr6:106233118 | T | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(341): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.573+15032A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233118 | ||||||
chr6:106233317 | C | G | 8 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0266others(5): Show | 8 | HG00621.hp2 HG00673.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+14833G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233317 | ||||||
chr6:106233687 | C | T | 346 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.573+14463G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233687 | ||||||
chr6:106233708 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.573+14442A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233708 | ||||||
chr6:106233757 | C | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+14393G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233757 | ||||||
chr6:106233774 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.573+14376G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233774 | ||||||
chr6:106233851 | A | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+14299T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106233851 | ||||||
chr6:106234010 | T | A | 1 | a0001c0001t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.573+14140A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234010 | ||||||
chr6:106234016 | T | C | 1 | a0001c0001t0006g0002 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.573+14134A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234016 | ||||||
chr6:106234035 | A | G | 1 | a0001c0003t0002g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.573+14115T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234035 | ||||||
chr6:106234115 | G | A | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+14035C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234115 | ||||||
chr6:106234165 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.573+13985G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234165 | ||||||
chr6:106234179 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.573+13971G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234179 | ||||||
chr6:106234210 | G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035 | 4 | NA18954.hp1 NA19062.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+13940C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234210 | ||||||
chr6:106234221 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+13929A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234221 | ||||||
chr6:106234849 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+13301A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106234849 | ||||||
chr6:106235003 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+13147C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235003 | ||||||
chr6:106235475 | GT | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+12674delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235475 | ||||||
chr6:106235477 | G | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+12673C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235477 | ||||||
chr6:106235479 | G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18977.hp2 NA19001.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.573+12671C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235479 | ||||||
chr6:106235482 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.573+12668C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235482 | ||||||
chr6:106235484 | C | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+12666G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235484 | ||||||
chr6:106235548 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+12602A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235548 | ||||||
chr6:106235734 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.573+12416C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235734 | ||||||
chr6:106235776 | GCTCT | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.573+12370_573+1237 others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235776 | ||||||
chr6:106235813 | C | CA | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(99): Show | 106 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.573+12336dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235813 | ||||||
chr6:106235814 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.573+12336T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235814 | ||||||
chr6:106235824 | T | C | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+12326A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106235824 | ||||||
chr6:106236001 | T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+12149A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236001 | ||||||
chr6:106236120 | T | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.573+12030A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236120 | ||||||
chr6:106236312 | T | C | 1 | a0001c0001t0001g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.573+11838A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236312 | ||||||
chr6:106236380 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.573+11770A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236380 | ||||||
chr6:106236578 | C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.573+11572G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236578 | ||||||
chr6:106236595 | C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 238 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.573+11555G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236595 | ||||||
chr6:106236780 | C | T | 1 | a0001c0001t0004g0095 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.573+11370G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106236780 | ||||||
chr6:106237320 | G | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+10830C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106237320 | ||||||
chr6:106237336 | A | G | 4 | a0001c0001t0001g0243a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | NA18946.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+10814T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106237336 | ||||||
chr6:106238451 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.573+9699T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238451 | ||||||
chr6:106238518 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.573+9632C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238518 | ||||||
chr6:106238543 | A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+9607T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238543 | ||||||
chr6:106238552 | A | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.573+9598T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238552 | ||||||
chr6:106238623 | C | G | 1 | a0001c0003t0002g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.573+9527G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238623 | ||||||
chr6:106238972 | T | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0044others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.573+9178A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106238972 | ||||||
chr6:106239190 | T | C | 1 | a0001c0001t0009g0330 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.573+8960A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239190 | ||||||
chr6:106239473 | T | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+8677A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239473 | ||||||
chr6:106239504 | A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 246 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.573+8646T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239504 | ||||||
chr6:106239547 | A | C | 2 | a0001c0003t0002g0011a0001c0003t0002g0013 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.573+8603T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239547 | ||||||
chr6:106239608 | T | C | 12 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01175.hp1 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.573+8542A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239608 | ||||||
chr6:106239698 | C | T | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.573+8452G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239698 | ||||||
chr6:106239935 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.573+8215A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239935 | ||||||
chr6:106239959 | T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0329 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.573+8191A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239959 | ||||||
chr6:106239990 | A | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+8160T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239990 | ||||||
chr6:106239994 | G | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+8156C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106239994 | ||||||
chr6:106240043 | A | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+8107T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240043 | ||||||
chr6:106240130 | G | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.573+8020C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240130 | ||||||
chr6:106240133 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+8017T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240133 | ||||||
chr6:106240237 | T | C | 2 | a0002c0002t0001g0052a0002c0002t0001g0053 | 2 | NA18965.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.573+7913A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240237 | ||||||
chr6:106240255 | C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0138 | 3 | NA18947.hp1 NA18969.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.573+7895G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240255 | ||||||
chr6:106240294 | C | T | 18 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 18 | HG01175.hp1 HG01346.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+7856G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240294 | ||||||
chr6:106240400 | T | TTAAA | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.573+7749_573+7750i others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240400 | ||||||
chr6:106240511 | ATTAG | A | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.573+7635_573+7638d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240511 | ||||||
chr6:106240777 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+7373T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240777 | ||||||
chr6:106240912 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.573+7238C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106240912 | ||||||
chr6:106241090 | T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG00738.hp1 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+7060A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106241090 | ||||||
chr6:106241192 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.573+6958T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106241192 | ||||||
chr6:106241506 | T | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+6644A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106241506 | ||||||
chr6:106241872 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+6278C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106241872 | ||||||
chr6:106241933 | A | G | 1 | a0001c0001t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.573+6217T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106241933 | ||||||
chr6:106242025 | A | C | 1 | a0001c0001t0001g0340 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.573+6125T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242025 | ||||||
chr6:106242045 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+6105A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242045 | ||||||
chr6:106242062 | G | GT | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+6087dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242062 | ||||||
chr6:106242067 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+6083A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242067 | ||||||
chr6:106242138 | TCA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(96): Show | 103 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.573+6010_573+6011d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242138 | ||||||
chr6:106242168 | C | G | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+5982G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242168 | ||||||
chr6:106242200 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.573+5950C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242200 | ||||||
chr6:106242223 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+5927C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242223 | ||||||
chr6:106242257 | T | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+5893A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242257 | ||||||
chr6:106242339 | T | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+5811A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242339 | ||||||
chr6:106242427 | G | A | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+5723C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242427 | ||||||
chr6:106242561 | ATTTAT | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+5584_573+5588d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242561 | ||||||
chr6:106242629 | C | CA | 37 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0075others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.573+5520dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242629 | ||||||
chr6:106242629 | CA | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0123 | 4 | HG02809.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+5520delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106242629 | ||||||
chr6:106243472 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.573+4678C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243472 | ||||||
chr6:106243526 | T | TG | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(170): Show | 180 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.573+4623dupC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243526 | ||||||
chr6:106243530 | G | GGA | 4 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0229others(1): Show | 4 | NA18906.hp1 NA19062.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+4619_573+4620i others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243530 | ||||||
chr6:106243530 | G | GGAA | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+4619_573+4620i others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243530 | ||||||
chr6:106243530 | GA | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0247others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+4619delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243530 | ||||||
chr6:106243708 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+4442C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243708 | ||||||
chr6:106243780 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.573+4370C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243780 | ||||||
chr6:106243838 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.573+4312T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243838 | ||||||
chr6:106243862 | A | T | 2 | a0001c0001t0001g0084a0001c0001t0012g0019 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.573+4288T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243862 | ||||||
chr6:106243904 | C | CT | 35 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(32): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.573+4245dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243904 | ||||||
chr6:106243904 | C | CTT | 12 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0030others(9): Show | 12 | HG01258.hp2 HG02040.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+4244_573+4245d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243904 | ||||||
chr6:106243904 | CT | C | 111 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0076others(108): Show | 112 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.573+4245delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243904 | ||||||
chr6:106243904 | CTT | C | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(147): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.573+4244_573+4245d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243904 | ||||||
chr6:106243904 | CTTT | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0091others(6): Show | 10 | HG01884.hp2 HG02451.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+4243_573+4245d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243904 | ||||||
chr6:106243931 | T | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(9): Show | 12 | HG00741.hp2 HG01169.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+4219A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106243931 | ||||||
chr6:106244075 | C | T | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573+4075G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244075 | ||||||
chr6:106244079 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573+4071A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244079 | ||||||
chr6:106244225 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.573+3925A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244225 | ||||||
chr6:106244280 | A | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+3870T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244280 | ||||||
chr6:106244440 | G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG00738.hp1 HG01516.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+3710C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244440 | ||||||
chr6:106244447 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+3703A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244447 | ||||||
chr6:106244472 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+3678G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244472 | ||||||
chr6:106244473 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+3677A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244473 | ||||||
chr6:106244474 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+3676T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244474 | ||||||
chr6:106244698 | T | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+3452A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244698 | ||||||
chr6:106244820 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+3330A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244820 | ||||||
chr6:106244918 | T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0264 | 2 | NA18959.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.573+3232A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244918 | ||||||
chr6:106244944 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.573+3206T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106244944 | ||||||
chr6:106245116 | A | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+3034T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245116 | ||||||
chr6:106245227 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+2923C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245227 | ||||||
chr6:106245229 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+2921G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245229 | ||||||
chr6:106245230 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+2920T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245230 | ||||||
chr6:106245239 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+2911A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245239 | ||||||
chr6:106245273 | G | C | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.573+2877C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245273 | ||||||
chr6:106245363 | A | C | 5 | a0001c0001t0001g0133a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG00609.hp1 NA18954.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2787T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245363 | ||||||
chr6:106245401 | T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 57 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.573+2749A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245401 | ||||||
chr6:106245423 | A | C | 1 | a0001c0001t0001g0338 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.573+2727T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245423 | ||||||
chr6:106245646 | G | A | 42 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(39): Show | 42 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.573+2504C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245646 | ||||||
chr6:106245695 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.573+2455T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245695 | ||||||
chr6:106245814 | A | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG00438.hp1 HG02155.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2336T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245814 | ||||||
chr6:106245958 | T | A | 2 | a0001c0001t0001g0282a0001c0001t0010g0284 | 2 | HG00642.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.573+2192A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106245958 | ||||||
chr6:106246067 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.573+2083A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246067 | ||||||
chr6:106246173 | T | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02135.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.573+1977A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246173 | ||||||
chr6:106246218 | AAGTGCCT others(16): Show |
A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.573+1909_573+1931d others(25): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246218 | ||||||
chr6:106246349 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.573+1801T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246349 | ||||||
chr6:106246371 | G | GTC | 5 | a0001c0001t0001g0255a0001c0001t0001g0260a0001c0001t0001g0266others(2): Show | 5 | HG00639.hp1 HG01884.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+1777_573+1778d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246371 | ||||||
chr6:106246371 | G | GTCTC | 15 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0258others(12): Show | 15 | HG00621.hp2 HG00673.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+1775_573+1778d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246371 | ||||||
chr6:106246371 | GTC | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0283a0001c0001t0012g0019 | 3 | HG02280.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.573+1777_573+1778d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246371 | ||||||
chr6:106246377 | C | G | 1 | a0001c0001t0001g0339 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.573+1773G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246377 | ||||||
chr6:106246386 | TCTCTCTC others(5): Show |
T | 1 | a0001c0001t0001g0033 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.573+1752_573+1763d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246386 | ||||||
chr6:106246388 | T | TCACACAC others(3): Show |
1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+1761_573+1762i others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246388 | ||||||
chr6:106246390 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+1760A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246390 | ||||||
chr6:106246390 | TCTCA | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0059a0001c0001t0001g0064others(11): Show | 14 | HG00438.hp1 HG00642.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.573+1756_573+1759d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246390 | ||||||
chr6:106246390 | TCTCACA | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 47 | HG00558.hp1 HG00621.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.573+1754_573+1759d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246390 | ||||||
chr6:106246390 | TCTCACAC others(1): Show |
T | 38 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0023others(35): Show | 42 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.573+1752_573+1759d others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246390 | ||||||
chr6:106246390 | TCTCACAC others(3): Show |
T | 2 | a0001c0001t0001g0025a0001c0001t0001g0049 | 2 | HG00408.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.573+1750_573+1759d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246390 | ||||||
chr6:106246392 | T | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(3): Show | 6 | HG02622.hp1 HG03486.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+1758A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | T | TCA | 8 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0107others(5): Show | 8 | HG01433.hp1 HG01934.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+1756_573+1757d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | T | TCACA | 3 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0106 | 3 | HG01346.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.573+1754_573+1757d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | T | TCACACA | 3 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0109 | 3 | HG01175.hp1 HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.573+1752_573+1757d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | T | TCTCTCA | 3 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0271 | 3 | HG02129.hp2 HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.573+1757_573+1758i others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | TCA | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.573+1756_573+1757d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | TCACA | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0071others(42): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+1754_573+1757d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | TCACACA | T | 9 | a0001c0001t0001g0089a0001c0001t0001g0135a0001c0001t0001g0193others(6): Show | 9 | HG00323.hp1 HG02083.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+1752_573+1757d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | TCACACAC others(3): Show |
T | 1 | a0001c0003t0002g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.573+1748_573+1757d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246392 | TCACACAC others(5): Show |
T | 5 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1746_573+1757d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246392 | ||||||
chr6:106246394 | A | T | 17 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0257others(14): Show | 17 | HG00621.hp2 HG00639.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.573+1756T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246394 | ||||||
chr6:106246396 | A | T | 19 | a0001c0001t0001g0093a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG01256.hp2 HG01346.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.573+1754T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246396 | ||||||
chr6:106246398 | A | T | 47 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(44): Show | 47 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.573+1752T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246398 | ||||||
chr6:106246400 | A | T | 42 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(39): Show | 42 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.573+1750T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246400 | ||||||
chr6:106246402 | A | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0295a0001c0001t0001g0297others(15): Show | 18 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.573+1748T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246402 | ||||||
chr6:106246430 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.573+1720T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246430 | ||||||
chr6:106246435 | TTC | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+1713_573+1714d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246435 | ||||||
chr6:106246535 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.573+1615T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246535 | ||||||
chr6:106246681 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.573+1469A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246681 | ||||||
chr6:106246725 | T | C | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0346 | 3 | HG01433.hp2 NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.573+1425A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246725 | ||||||
chr6:106246745 | T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0103others(1): Show | 4 | HG01175.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1405A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246745 | ||||||
chr6:106246887 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.573+1263T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106246887 | ||||||
chr6:106247085 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+1065G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247085 | ||||||
chr6:106247431 | A | T | 1 | a0001c0001t0001g0338 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.573+719T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247431 | ||||||
chr6:106247447 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+703A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247447 | ||||||
chr6:106247525 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+625T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247525 | ||||||
chr6:106247594 | G | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+556C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247594 | ||||||
chr6:106247710 | T | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(341): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.573+440A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247710 | ||||||
chr6:106247750 | T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18977.hp2 NA19001.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.573+400A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247750 | ||||||
chr6:106247785 | A | T | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.573+365T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106247785 | ||||||
chr6:106248104 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.573+46A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 6/7 | chr6 | 106248104 | ||||||
chr6:106248564 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.479-320A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106248564 | ||||||
chr6:106248842 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-598C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106248842 | ||||||
chr6:106248985 | T | A | 1 | a0001c0001t0001g0338 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.479-741A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106248985 | ||||||
chr6:106249006 | A | T | 1 | a0001c0001t0001g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.479-762T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249006 | ||||||
chr6:106249191 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.479-947T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249191 | ||||||
chr6:106249192 | T | C | 1 | a0001c0003t0002g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.479-948A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249192 | ||||||
chr6:106249197 | AG | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.479-954delC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249197 | ||||||
chr6:106249370 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-1126C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249370 | ||||||
chr6:106249458 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-1214G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249458 | ||||||
chr6:106249499 | T | C | 2 | a0001c0003t0002g0011a0001c0003t0002g0013 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.479-1255A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249499 | ||||||
chr6:106249517 | C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.479-1273G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249517 | ||||||
chr6:106249735 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.479-1491A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249735 | ||||||
chr6:106249797 | T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(184): Show | 194 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.479-1553A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106249797 | ||||||
chr6:106250011 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.479-1767A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250011 | ||||||
chr6:106250055 | CT | C | 7 | a0001c0001t0001g0047a0001c0003t0002g0011a0001c0003t0002g0012others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.479-1812delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250055 | ||||||
chr6:106250174 | G | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0233 | 2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.479-1930C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250174 | ||||||
chr6:106250177 | AT | A | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.479-1934delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250177 | ||||||
chr6:106250208 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.479-1964T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250208 | ||||||
chr6:106250264 | A | AATTAGTT | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-2021_479-2020i others(9): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250264 | ||||||
chr6:106250650 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.479-2406T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250650 | ||||||
chr6:106250676 | A | T | 1 | a0001c0001t0001g0241 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.479-2432T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250676 | ||||||
chr6:106250919 | C | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-2675G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250919 | ||||||
chr6:106250985 | ATACGCAA others(7): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.479-2755_479-2742d others(16): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106250985 | ||||||
chr6:106251320 | T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0113 | 3 | HG00099.hp1 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.479-3076A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251320 | ||||||
chr6:106251402 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.479-3158A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251402 | ||||||
chr6:106251515 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.479-3271C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251515 | ||||||
chr6:106251546 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.479-3302A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251546 | ||||||
chr6:106251577 | G | A | 5 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01891.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-3333C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251577 | ||||||
chr6:106251640 | A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.479-3396T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251640 | ||||||
chr6:106251642 | A | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-3398T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251642 | ||||||
chr6:106251644 | A | AGAGAGAG others(260): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0113 | 3 | HG00099.hp1 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.479-3401_479-3400i others(269): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGAGGGAG others(278): Show |
1 | a0001c0001t0001g0029 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(287): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(226): Show |
1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(235): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(334): Show |
1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(343): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(296): Show |
3 | a0001c0001t0001g0263a0001c0001t0001g0272a0001c0001t0001g0331 | 3 | HG00621.hp2 HG02129.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.479-3401_479-3400i others(305): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(292): Show |
21 | a0001c0001t0001g0071a0001c0001t0001g0102a0001c0001t0001g0104others(18): Show | 21 | HG00639.hp1 HG00673.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.479-3401_479-3400i others(301): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(291): Show |
1 | a0001c0001t0001g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(300): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(292): Show |
1 | a0001c0001t0001g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.479-3401_479-3400i others(301): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(293): Show |
1 | a0001c0001t0001g0274 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(302): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(293): Show |
1 | a0001c0001t0001g0273 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.479-3401_479-3400i others(302): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(266): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0106 | 3 | HG01175.hp1 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.479-3401_479-3400i others(275): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(267): Show |
1 | a0001c0001t0001g0075 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.479-3401_479-3400i others(276): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(293): Show |
1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(302): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(299): Show |
1 | a0001c0001t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(308): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(296): Show |
1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(305): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGAGGG others(299): Show |
1 | a0001c0001t0001g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.479-3401_479-3400i others(308): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGGGAG others(308): Show |
1 | a0001c0003t0002g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.479-3401_479-3400i others(317): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGGGAG others(309): Show |
1 | a0001c0003t0002g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(318): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGGGAG others(315): Show |
1 | a0001c0003t0002g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(324): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | AGGGGGAG others(332): Show |
1 | a0001c0003t0002g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.479-3401_479-3400i others(341): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251644 | A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.479-3400T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251644 | ||||||
chr6:106251647 | G | GGGAGGGA others(273): Show |
1 | a0001c0001t0001g0070 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.479-3404_479-3403i others(282): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251647 | ||||||
chr6:106251648 | G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0075others(41): Show | 45 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.479-3404C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(266): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(275): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(260): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0208 | 3 | NA18939.hp1 NA19011.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(269): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(268): Show |
1 | a0001c0001t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(277): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(263): Show |
2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA18962.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(272): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(330): Show |
2 | a0001c0001t0005g0333a0001c0001t0005g0335 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(339): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(290): Show |
1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(299): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(277): Show |
1 | a0002c0002t0001g0052 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(286): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(278): Show |
42 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(39): Show | 46 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.479-3405_479-3404i others(287): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(279): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0045 | 2 | HG02273.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(288): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(280): Show |
1 | a0001c0001t0001g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(289): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(285): Show |
1 | a0001c0001t0001g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(294): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(279): Show |
1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(288): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(312): Show |
1 | a0001c0001t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(321): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(279): Show |
1 | a0001c0001t0001g0228 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(288): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(272): Show |
21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0072others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.479-3405_479-3404i others(281): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(268): Show |
57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 60 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.479-3405_479-3404i others(277): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(282): Show |
1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(291): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(270): Show |
1 | a0001c0001t0001g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(279): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(267): Show |
1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(276): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(264): Show |
1 | a0001c0001t0001g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(273): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(264): Show |
1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(273): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(258): Show |
1 | a0001c0001t0001g0314 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(267): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(263): Show |
1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(272): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(246): Show |
1 | a0001c0001t0001g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(255): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(264): Show |
135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(132): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.479-3405_479-3404i others(273): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
1 | a0001c0001t0001g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(260): Show |
1 | a0001c0001t0001g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(269): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
1 | a0001c0001t0001g0203 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
1 | a0001c0001t0001g0154 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
1 | a0001c0001t0011g0248 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
1 | a0001c0001t0001g0305 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(261): Show |
1 | a0001c0001t0001g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(270): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0338 | 2 | NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(285): Show |
1 | a0001c0001t0001g0027 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(294): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(279): Show |
1 | a0001c0001t0001g0030 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.479-3405_479-3404i others(288): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(271): Show |
1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(280): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(265): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0196 | 2 | HG03942.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.479-3405_479-3404i others(274): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(332): Show |
1 | a0001c0001t0005g0336 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(341): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(272): Show |
1 | a0001c0001t0001g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(281): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251648 | G | GGAGGGAG others(272): Show |
1 | a0001c0001t0001g0286 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.479-3405_479-3404i others(281): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251648 | ||||||
chr6:106251661 | A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0001g0302 | 4 | HG00738.hp2 HG01109.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-3417T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251661 | ||||||
chr6:106251666 | A | AGGGAGGC others(279): Show |
1 | a0001c0001t0001g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.479-3423_479-3422i others(288): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251666 | ||||||
chr6:106251667 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.479-3423C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251667 | ||||||
chr6:106251668 | G | GGAGGCGG others(254): Show |
1 | a0001c0001t0001g0302 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.479-3425_479-3424i others(263): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251668 | ||||||
chr6:106251672 | A | AG | 5 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0201others(2): Show | 5 | HG01109.hp2 NA18949.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-3429dupC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251672 | ||||||
chr6:106251691 | CAGAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.479-3459_479-3448d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251691 | ||||||
chr6:106251764 | AAAG | A | 3 | a0001c0001t0012g0019a0001c0003t0002g0011a0001c0003t0002g0013 | 3 | HG01891.hp1 HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.479-3523_479-3521d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251764 | ||||||
chr6:106251842 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.479-3598A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251842 | ||||||
chr6:106251850 | T | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-3606A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251850 | ||||||
chr6:106251854 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.479-3610T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251854 | ||||||
chr6:106251997 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.479-3753G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251997 | ||||||
chr6:106251998 | G | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0044others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.479-3754C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106251998 | ||||||
chr6:106252048 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.479-3804G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252048 | ||||||
chr6:106252131 | T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0093 | 2 | HG02273.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.479-3887A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252131 | ||||||
chr6:106252187 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.479-3943A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252187 | ||||||
chr6:106252273 | A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(51): Show | 58 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.479-4029T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252273 | ||||||
chr6:106252330 | A | T | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-4086T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252330 | ||||||
chr6:106252349 | TA | T | 9 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0166others(6): Show | 10 | HG01169.hp1 HG01169.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-4106delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252349 | ||||||
chr6:106252439 | A | G | 2 | a0001c0003t0002g0011a0001c0003t0002g0013 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.479-4195T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252439 | ||||||
chr6:106252567 | A | C | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-4323T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252567 | ||||||
chr6:106252716 | T | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.479-4472A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252716 | ||||||
chr6:106252729 | T | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 65 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.479-4485A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252729 | ||||||
chr6:106252751 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.479-4507A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252751 | ||||||
chr6:106252822 | A | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-4578T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106252822 | ||||||
chr6:106253094 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-4850A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253094 | ||||||
chr6:106253396 | TA | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.479-5153delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253396 | ||||||
chr6:106253421 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.479-5177A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253421 | ||||||
chr6:106253428 | C | T | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.479-5184G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253428 | ||||||
chr6:106253443 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5199G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253443 | ||||||
chr6:106253446 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5202T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253446 | ||||||
chr6:106253448 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5204A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253448 | ||||||
chr6:106253450 | C | G | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5206G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253450 | ||||||
chr6:106253451 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5207G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253451 | ||||||
chr6:106253457 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5213T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253457 | ||||||
chr6:106253458 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.479-5214T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253458 | ||||||
chr6:106253461 | G | T | 42 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(39): Show | 42 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.479-5217C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253461 | ||||||
chr6:106253529 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479-5285T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253529 | ||||||
chr6:106253559 | G | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-5315C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253559 | ||||||
chr6:106253601 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.479-5357G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253601 | ||||||
chr6:106253809 | A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.479-5565T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253809 | ||||||
chr6:106253968 | T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(184): Show | 194 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.479-5724A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106253968 | ||||||
chr6:106254240 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-5996A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254240 | ||||||
chr6:106254248 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-6004A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254248 | ||||||
chr6:106254359 | G | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-6115C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254359 | ||||||
chr6:106254370 | G | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 65 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.479-6126C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254370 | ||||||
chr6:106254409 | G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG02135.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.479-6165C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254409 | ||||||
chr6:106254451 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.479-6207A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254451 | ||||||
chr6:106254472 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-6228A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254472 | ||||||
chr6:106254902 | T | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.479-6658A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106254902 | ||||||
chr6:106255263 | T | G | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.479-7019A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255263 | ||||||
chr6:106255316 | G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | NA18946.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-7072C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255316 | ||||||
chr6:106255611 | C | T | 3 | a0001c0001t0005g0333a0001c0001t0005g0335a0001c0001t0005g0336 | 3 | HG02970.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.479-7367G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255611 | ||||||
chr6:106255743 | T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(51): Show | 58 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.479-7499A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255743 | ||||||
chr6:106255844 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.479-7600C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255844 | ||||||
chr6:106255852 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.479-7608G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106255852 | ||||||
chr6:106256193 | T | TA | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-7950dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256193 | ||||||
chr6:106256548 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-8304C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256548 | ||||||
chr6:106256573 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.479-8329G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256573 | ||||||
chr6:106256597 | C | CTAGAGAG others(17): Show |
1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.479-8377_479-8354d others(26): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256597 | ||||||
chr6:106256619 | C | A | 45 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(42): Show | 45 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.479-8375G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256619 | ||||||
chr6:106256687 | A | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.479-8443T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256687 | ||||||
chr6:106256726 | G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0043 | 2 | HG01074.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.479-8482C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256726 | ||||||
chr6:106256749 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.479-8505G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106256749 | ||||||
chr6:106257052 | A | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(51): Show | 58 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.479-8808T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257052 | ||||||
chr6:106257116 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.479-8872A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257116 | ||||||
chr6:106257150 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.479-8906C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257150 | ||||||
chr6:106257506 | A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01255.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.479-9262T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257506 | ||||||
chr6:106257570 | C | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-9326G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257570 | ||||||
chr6:106257603 | T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.479-9359A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257603 | ||||||
chr6:106257911 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479-9667A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106257911 | ||||||
chr6:106258331 | C | T | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0346 | 3 | HG01433.hp2 NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.479-10087G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106258331 | ||||||
chr6:106258359 | C | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-10115G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106258359 | ||||||
chr6:106258581 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.479-10337A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106258581 | ||||||
chr6:106258771 | C | T | 9 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00408.hp1 NA18950.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.479-10527G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106258771 | ||||||
chr6:106259007 | T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 57 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.479-10763A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259007 | ||||||
chr6:106259021 | C | CAGTT | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(223): Show | 233 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.479-10778_479-1077 others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259021 | ||||||
chr6:106259127 | A | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.479-10883T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259127 | ||||||
chr6:106259142 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.479-10898G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259142 | ||||||
chr6:106259431 | T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0171 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.479-11187A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259431 | ||||||
chr6:106259630 | T | C | 6 | a0001c0001t0001g0249a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-11386A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259630 | ||||||
chr6:106259794 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.479-11550G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259794 | ||||||
chr6:106259794 | CAAGAAGA others(6): Show |
C | 2 | a0001c0001t0001g0132a0001c0001t0001g0139 | 2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.479-11563_479-1155 others(17): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259794 | ||||||
chr6:106259873 | T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.479-11629A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259873 | ||||||
chr6:106259905 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-11661A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106259905 | ||||||
chr6:106260043 | G | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG00738.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.479-11799C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260043 | ||||||
chr6:106260043 | G | T | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-11799C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260043 | ||||||
chr6:106260105 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.479-11861G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260105 | ||||||
chr6:106260197 | T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0189 | 2 | NA18967.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.479-11953A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260197 | ||||||
chr6:106260466 | T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0139 | 2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.479-12222A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260466 | ||||||
chr6:106260919 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.479-12675C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260919 | ||||||
chr6:106260938 | C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.479-12694G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260938 | ||||||
chr6:106260949 | T | C | 35 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(32): Show | 35 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.479-12705A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106260949 | ||||||
chr6:106261086 | G | A | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.479-12842C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261086 | ||||||
chr6:106261096 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.479-12852T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261096 | ||||||
chr6:106261375 | C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0344 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.479-13131G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261375 | ||||||
chr6:106261429 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.479-13185A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261429 | ||||||
chr6:106261448 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.479-13204A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261448 | ||||||
chr6:106261537 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-13293C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261537 | ||||||
chr6:106261709 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479-13465A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261709 | ||||||
chr6:106261869 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.479-13625A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261869 | ||||||
chr6:106261981 | A | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.479-13737T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106261981 | ||||||
chr6:106262124 | G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.479-13880C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262124 | ||||||
chr6:106262158 | C | T | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.479-13914G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262158 | ||||||
chr6:106262217 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.479-13973G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262217 | ||||||
chr6:106262315 | C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.479-14071G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262315 | ||||||
chr6:106262400 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-14156T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262400 | ||||||
chr6:106262443 | A | C | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479-14199T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262443 | ||||||
chr6:106262491 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.479-14247C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262491 | ||||||
chr6:106262556 | G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.479-14312C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262556 | ||||||
chr6:106262688 | T | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-14444A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262688 | ||||||
chr6:106262743 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.479-14499C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262743 | ||||||
chr6:106262770 | T | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-14526A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262770 | ||||||
chr6:106262791 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-14547A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262791 | ||||||
chr6:106262808 | C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 57 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.479-14564G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262808 | ||||||
chr6:106262856 | G | A | 2 | a0001c0004t0002g0015a0001c0004t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.479-14612C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262856 | ||||||
chr6:106262972 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.479-14728C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262972 | ||||||
chr6:106262993 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.479-14749C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106262993 | ||||||
chr6:106263068 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.479-14824C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263068 | ||||||
chr6:106263091 | C | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.479-14847G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263091 | ||||||
chr6:106263171 | G | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-14927C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263171 | ||||||
chr6:106263214 | T | C | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-14970A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263214 | ||||||
chr6:106263222 | C | G | 2 | a0001c0004t0002g0015a0001c0004t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.479-14978G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263222 | ||||||
chr6:106263336 | C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0176 | 3 | HG00642.hp1 HG02258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.479-15092G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263336 | ||||||
chr6:106263466 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.479-15222A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263466 | ||||||
chr6:106263518 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.479-15274C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263518 | ||||||
chr6:106263640 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.479-15396G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263640 | ||||||
chr6:106263641 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.479-15397C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263641 | ||||||
chr6:106263808 | C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0264 | 2 | NA18959.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.479-15564G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263808 | ||||||
chr6:106263878 | G | GA | 72 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0070others(69): Show | 72 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.479-15635dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263878 | ||||||
chr6:106263898 | A | G | 42 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(39): Show | 42 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.479-15654T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263898 | ||||||
chr6:106263906 | G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0149 | 3 | NA18944.hp1 NA18948.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.479-15662C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106263906 | ||||||
chr6:106264012 | A | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+15649T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264012 | ||||||
chr6:106264013 | A | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+15648T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264013 | ||||||
chr6:106264426 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.478+15235A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264426 | ||||||
chr6:106264473 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.478+15188A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264473 | ||||||
chr6:106264712 | T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0309 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.478+14949A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264712 | ||||||
chr6:106264755 | C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.478+14906G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264755 | ||||||
chr6:106264807 | A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0286 | 2 | HG00558.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.478+14854T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264807 | ||||||
chr6:106264851 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.478+14810A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264851 | ||||||
chr6:106264971 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.478+14690C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106264971 | ||||||
chr6:106265168 | C | CA | 16 | a0001c0001t0001g0154a0001c0001t0001g0194a0001c0001t0001g0228others(13): Show | 16 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.478+14492dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265168 | ||||||
chr6:106265168 | CA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(56): Show | 63 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.478+14492delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265168 | ||||||
chr6:106265192 | G | A | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.478+14469C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265192 | ||||||
chr6:106265387 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.478+14274G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265387 | ||||||
chr6:106265408 | A | G | 2 | a0001c0004t0002g0015a0001c0004t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.478+14253T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265408 | ||||||
chr6:106265444 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.478+14217G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265444 | ||||||
chr6:106265507 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.478+14154A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265507 | ||||||
chr6:106265574 | G | T | 2 | a0001c0001t0007g0205a0001c0001t0007g0212 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.478+14087C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265574 | ||||||
chr6:106265588 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.478+14073G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265588 | ||||||
chr6:106265637 | G | A | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478+14024C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265637 | ||||||
chr6:106265706 | C | T | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+13955G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265706 | ||||||
chr6:106265732 | G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.478+13929C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265732 | ||||||
chr6:106265816 | G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+13845C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265816 | ||||||
chr6:106265932 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.478+13729T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106265932 | ||||||
chr6:106266011 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.478+13650C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266011 | ||||||
chr6:106266034 | C | CA | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(53): Show | 60 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.478+13626dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266034 | ||||||
chr6:106266288 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+13373G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266288 | ||||||
chr6:106266388 | G | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+13273C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266388 | ||||||
chr6:106266482 | TCCCTAAC others(13): Show |
T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+13159_478+1317 others(24): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266482 | ||||||
chr6:106266816 | A | C | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478+12845T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106266816 | ||||||
chr6:106267130 | T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 190 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.478+12531A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267130 | ||||||
chr6:106267131 | A | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.478+12530T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267131 | ||||||
chr6:106267199 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.478+12462C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267199 | ||||||
chr6:106267231 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.478+12430G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267231 | ||||||
chr6:106267290 | C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.478+12371G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267290 | ||||||
chr6:106267385 | A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+12276T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267385 | ||||||
chr6:106267407 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.478+12254A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267407 | ||||||
chr6:106267435 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+12226G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267435 | ||||||
chr6:106267543 | G | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 59 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.478+12118C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267543 | ||||||
chr6:106267570 | T | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.478+12091A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267570 | ||||||
chr6:106267596 | A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0123 | 4 | HG02809.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+12065T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267596 | ||||||
chr6:106267603 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.478+12058G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267603 | ||||||
chr6:106267642 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.478+12019T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267642 | ||||||
chr6:106267710 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.478+11951C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267710 | ||||||
chr6:106267921 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.478+11740A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106267921 | ||||||
chr6:106268172 | T | TA | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+11488dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106268172 | ||||||
chr6:106268467 | G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG00673.hp1 NA18971.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+11194C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106268467 | ||||||
chr6:106268540 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.478+11121C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106268540 | ||||||
chr6:106269193 | G | T | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 60 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.478+10468C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269193 | ||||||
chr6:106269278 | C | A | 1 | a0001c0001t0001g0338 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.478+10383G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269278 | ||||||
chr6:106269395 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.478+10266C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269395 | ||||||
chr6:106269400 | G | GC | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.478+10260dupG | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269400 | ||||||
chr6:106269445 | G | A | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.478+10216C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269445 | ||||||
chr6:106269482 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.478+10179G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269482 | ||||||
chr6:106269540 | G | A | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.478+10121C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269540 | ||||||
chr6:106269668 | C | T | 1 | a0001c0001t0003g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.478+9993G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269668 | ||||||
chr6:106269696 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+9965G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269696 | ||||||
chr6:106269746 | G | A | 29 | a0001c0001t0001g0069a0001c0001t0001g0295a0001c0001t0001g0297others(26): Show | 29 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.478+9915C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269746 | ||||||
chr6:106269756 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.478+9905G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269756 | ||||||
chr6:106269778 | G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.478+9883C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269778 | ||||||
chr6:106269783 | TCTCCCTC others(5): Show |
T | 1 | a0001c0001t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.478+9866_478+9877d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106269783 | ||||||
chr6:106270133 | CCTT | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0123 | 4 | HG02809.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+9525_478+9527d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270133 | ||||||
chr6:106270322 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.478+9339T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270322 | ||||||
chr6:106270438 | T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+9223A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270438 | ||||||
chr6:106270647 | C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG00741.hp2 HG01169.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.478+9014G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270647 | ||||||
chr6:106270817 | C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 19 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.478+8844G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270817 | ||||||
chr6:106270827 | G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.478+8834C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106270827 | ||||||
chr6:106271018 | T | C | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.478+8643A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271018 | ||||||
chr6:106271057 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.478+8604A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271057 | ||||||
chr6:106271184 | G | A | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.478+8477C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271184 | ||||||
chr6:106271206 | A | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.478+8455T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271206 | ||||||
chr6:106271363 | G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+8298C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271363 | ||||||
chr6:106271529 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.478+8132C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271529 | ||||||
chr6:106271565 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+8096A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271565 | ||||||
chr6:106271610 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.478+8051A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271610 | ||||||
chr6:106271621 | A | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+8040T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271621 | ||||||
chr6:106271631 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.478+8030G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271631 | ||||||
chr6:106271789 | T | TA | 45 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(42): Show | 45 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.478+7871dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271789 | ||||||
chr6:106271864 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.478+7797A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271864 | ||||||
chr6:106271889 | G | A | 2 | a0001c0001t0001g0071a0001c0001t0012g0019 | 2 | HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.478+7772C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271889 | ||||||
chr6:106271950 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.478+7711A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271950 | ||||||
chr6:106271971 | A | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0291 | 2 | HG02083.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.478+7690T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106271971 | ||||||
chr6:106272087 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.478+7574G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272087 | ||||||
chr6:106272161 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.478+7500A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272161 | ||||||
chr6:106272435 | C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0286 | 3 | HG00558.hp1 NA18945.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.478+7226G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272435 | ||||||
chr6:106272470 | A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+7191T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272470 | ||||||
chr6:106272556 | A | T | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.478+7105T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272556 | ||||||
chr6:106272656 | G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+7005C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272656 | ||||||
chr6:106272870 | G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA18973.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.478+6791C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272870 | ||||||
chr6:106272954 | C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 50 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.478+6707G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106272954 | ||||||
chr6:106273037 | T | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.478+6624A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106273037 | ||||||
chr6:106273314 | CTA | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG00673.hp1 NA18971.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+6345_478+6346d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106273314 | ||||||
chr6:106273614 | GAAAGA | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+6042_478+6046d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106273614 | ||||||
chr6:106274291 | A | C | 19 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0074others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.478+5370T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274291 | ||||||
chr6:106274331 | A | G | 19 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0074others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.478+5330T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274331 | ||||||
chr6:106274342 | TA | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0077others(20): Show | 24 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.478+5318delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274342 | ||||||
chr6:106274585 | T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0231others(1): Show | 5 | NA18947.hp2 NA18948.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+5076A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274585 | ||||||
chr6:106274677 | CTTTAGT | C | 8 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | NA18972.hp1 NA18978.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+4978_478+4983d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274677 | ||||||
chr6:106274741 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+4920C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274741 | ||||||
chr6:106274800 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.478+4861G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274800 | ||||||
chr6:106274816 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.478+4845C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106274816 | ||||||
chr6:106275003 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.478+4658C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275003 | ||||||
chr6:106275120 | T | C | 1 | a0001c0001t0001g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.478+4541A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275120 | ||||||
chr6:106275303 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.478+4358G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275303 | ||||||
chr6:106275352 | C | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+4309G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275352 | ||||||
chr6:106275751 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.478+3910A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275751 | ||||||
chr6:106275937 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478+3724T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106275937 | ||||||
chr6:106276260 | C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01071.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.478+3401G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276260 | ||||||
chr6:106276261 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.478+3400C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276261 | ||||||
chr6:106276369 | C | T | 6 | a0001c0001t0001g0247a0001c0001t0001g0300a0001c0001t0001g0305others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+3292G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276369 | ||||||
chr6:106276464 | C | CA | 106 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(103): Show | 109 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.478+3196dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276464 | ||||||
chr6:106276464 | C | CAA | 7 | a0001c0001t0001g0188a0001c0001t0004g0095a0001c0001t0004g0096others(4): Show | 7 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+3195_478+3196d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276464 | ||||||
chr6:106276464 | C | CAAAA | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(42): Show | 49 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.478+3193_478+3196d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276464 | ||||||
chr6:106276464 | C | CAAAAA | 7 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG02135.hp1 NA18944.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+3192_478+3196d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276464 | ||||||
chr6:106276767 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.478+2894C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276767 | ||||||
chr6:106276948 | C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.478+2713G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106276948 | ||||||
chr6:106277458 | G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099others(3): Show | 8 | NA18962.hp1 NA18964.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+2203C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277458 | ||||||
chr6:106277541 | A | G | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+2120T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277541 | ||||||
chr6:106277808 | C | A | 1 | a0001c0003t0002g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.478+1853G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277808 | ||||||
chr6:106277830 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.478+1831T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277830 | ||||||
chr6:106277908 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+1753T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277908 | ||||||
chr6:106277996 | G | A | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.478+1665C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106277996 | ||||||
chr6:106278089 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.478+1572G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278089 | ||||||
chr6:106278241 | C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0027 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.478+1420G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278241 | ||||||
chr6:106278251 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.478+1410A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278251 | ||||||
chr6:106278297 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.478+1364C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278297 | ||||||
chr6:106278504 | T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.478+1157A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278504 | ||||||
chr6:106278640 | T | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0001t0001g0168 | 3 | HG02698.hp2 HG03669.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.478+1021A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278640 | ||||||
chr6:106278642 | T | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.478+1019A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278642 | ||||||
chr6:106278777 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478+884C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278777 | ||||||
chr6:106278810 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+851T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278810 | ||||||
chr6:106278952 | G | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.478+709C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278952 | ||||||
chr6:106278954 | TTAATATA others(3): Show |
T | 1 | a0002c0002t0001g0051 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.478+697_478+706del others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106278954 | ||||||
chr6:106279030 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.478+631T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106279030 | ||||||
chr6:106279340 | C | T | 21 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.478+321G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106279340 | ||||||
chr6:106279372 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+289T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106279372 | ||||||
chr6:106279481 | A | AG | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(181): Show | 191 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.478+179dupC | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106279481 | ||||||
chr6:106279556 | T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0293 | 3 | HG02572.hp1 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.478+105A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 5/7 | chr6 | 106279556 | ||||||
chr6:106279837 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-14T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106279837 | ||||||
chr6:106279844 | C | T | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.316-21G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106279844 | ||||||
chr6:106280274 | C | CA | 13 | a0001c0001t0001g0038a0001c0001t0001g0292a0001c0001t0001g0296others(10): Show | 13 | HG00738.hp2 HG01109.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.316-452dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280274 | ||||||
chr6:106280274 | CA | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0092others(5): Show | 9 | HG00642.hp2 HG01169.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-452delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280274 | ||||||
chr6:106280475 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.316-652T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280475 | ||||||
chr6:106280562 | CA | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.316-740delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280562 | ||||||
chr6:106280701 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.316-878T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280701 | ||||||
chr6:106280820 | T | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0113a0001c0001t0001g0124others(4): Show | 8 | HG00099.hp1 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-997A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280820 | ||||||
chr6:106280993 | C | CA | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-1171dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106280993 | ||||||
chr6:106281488 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.316-1665C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106281488 | ||||||
chr6:106281580 | T | A | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.316-1757A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106281580 | ||||||
chr6:106281713 | T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 238 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.316-1890A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106281713 | ||||||
chr6:106281998 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.316-2175A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106281998 | ||||||
chr6:106282009 | T | C | 6 | a0001c0001t0001g0237a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-2186A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282009 | ||||||
chr6:106282183 | A | C | 22 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(19): Show | 22 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.316-2360T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282183 | ||||||
chr6:106282248 | A | G | 41 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0071others(38): Show | 41 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.316-2425T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282248 | ||||||
chr6:106282262 | G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00408.hp1 NA18950.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-2439C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282262 | ||||||
chr6:106282863 | T | TGCA | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.316-3043_316-3041d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282863 | ||||||
chr6:106282893 | C | T | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.316-3070G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106282893 | ||||||
chr6:106283125 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.316-3302A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283125 | ||||||
chr6:106283516 | G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0300a0001c0001t0001g0305others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-3693C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283516 | ||||||
chr6:106283605 | T | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.316-3782A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283605 | ||||||
chr6:106283702 | C | T | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | NA18961.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.316-3879G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283702 | ||||||
chr6:106283704 | C | T | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.316-3881G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283704 | ||||||
chr6:106283705 | G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0167others(2): Show | 5 | NA18939.hp1 NA18968.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-3882C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283705 | ||||||
chr6:106283865 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.316-4042A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106283865 | ||||||
chr6:106284045 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-4222T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284045 | ||||||
chr6:106284052 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.316-4229C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284052 | ||||||
chr6:106284233 | T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0139 | 2 | NA18949.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.316-4410A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284233 | ||||||
chr6:106284250 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316-4427G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284250 | ||||||
chr6:106284272 | T | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.316-4449A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284272 | ||||||
chr6:106284276 | C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-4453G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284276 | ||||||
chr6:106284363 | G | GT | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-4541dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284363 | ||||||
chr6:106284508 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.316-4685G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284508 | ||||||
chr6:106284534 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-4711A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284534 | ||||||
chr6:106284555 | AT | A | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.316-4733delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284555 | ||||||
chr6:106284656 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.316-4833A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284656 | ||||||
chr6:106284658 | T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 62 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.316-4835A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284658 | ||||||
chr6:106284709 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.316-4886C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284709 | ||||||
chr6:106284728 | G | GT | 18 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0060others(15): Show | 19 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.316-4906dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284728 | ||||||
chr6:106284733 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316-4910A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284733 | ||||||
chr6:106284884 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.316-5061C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106284884 | ||||||
chr6:106285084 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316-5261C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285084 | ||||||
chr6:106285138 | C | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0229others(4): Show | 8 | HG02155.hp2 NA18947.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-5315G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285138 | ||||||
chr6:106285155 | T | C | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.316-5332A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285155 | ||||||
chr6:106285251 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-5428T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285251 | ||||||
chr6:106285308 | G | A | 1 | a0001c0001t0011g0248 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.316-5485C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285308 | ||||||
chr6:106285341 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.316-5518A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285341 | ||||||
chr6:106285373 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.316-5550T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285373 | ||||||
chr6:106285965 | TATGTAGC others(157): Show |
T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.316-6306_316-6143d others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106285965 | ||||||
chr6:106286078 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.316-6255A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286078 | ||||||
chr6:106286144 | T | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01496.hp1 HG02165.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-6321A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286144 | ||||||
chr6:106286165 | C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 185 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.316-6342G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286165 | ||||||
chr6:106286214 | A | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.316-6391T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286214 | ||||||
chr6:106286277 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.316-6454C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286277 | ||||||
chr6:106286308 | ATGGG | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-6489_316-6486d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286308 | ||||||
chr6:106286313 | G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-6490C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286313 | ||||||
chr6:106286314 | C | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-6491G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286314 | ||||||
chr6:106286314 | C | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.316-6491G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286314 | ||||||
chr6:106286533 | T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(222): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.315+6495A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286533 | ||||||
chr6:106286797 | C | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0317 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.315+6231G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286797 | ||||||
chr6:106286825 | C | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+6203G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286825 | ||||||
chr6:106286911 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+6117C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286911 | ||||||
chr6:106286988 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.315+6040T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106286988 | ||||||
chr6:106287100 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.315+5928T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287100 | ||||||
chr6:106287476 | T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA18973.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.315+5552A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287476 | ||||||
chr6:106287609 | A | G | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.315+5419T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287609 | ||||||
chr6:106287618 | A | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+5410T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287618 | ||||||
chr6:106287626 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.315+5402A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287626 | ||||||
chr6:106287789 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.315+5239T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287789 | ||||||
chr6:106287845 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+5183C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287845 | ||||||
chr6:106287865 | A | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+5163T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287865 | ||||||
chr6:106287974 | C | CT | 6 | a0001c0001t0001g0132a0001c0001t0001g0150a0001c0001t0005g0333others(3): Show | 6 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+5053dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287974 | ||||||
chr6:106287975 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.315+5053A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106287975 | ||||||
chr6:106288076 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.315+4952A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288076 | ||||||
chr6:106288130 | C | T | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.315+4898G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288130 | ||||||
chr6:106288138 | T | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.315+4890A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288138 | ||||||
chr6:106288252 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+4776C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288252 | ||||||
chr6:106288456 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.315+4572A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288456 | ||||||
chr6:106288487 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.315+4541T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288487 | ||||||
chr6:106288567 | G | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+4461C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288567 | ||||||
chr6:106288640 | G | A | 2 | a0001c0001t0005g0335a0001c0001t0005g0336 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.315+4388C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288640 | ||||||
chr6:106288924 | A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.315+4104T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288924 | ||||||
chr6:106288934 | A | ATG | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.315+4092_315+4093d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288934 | ||||||
chr6:106288985 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.315+4043A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106288985 | ||||||
chr6:106289032 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.315+3996A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289032 | ||||||
chr6:106289049 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.315+3979T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289049 | ||||||
chr6:106289275 | A | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+3753T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289275 | ||||||
chr6:106289402 | G | GA | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.315+3625dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289402 | ||||||
chr6:106289475 | A | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.315+3553T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289475 | ||||||
chr6:106289531 | G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0044others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.315+3497C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289531 | ||||||
chr6:106289553 | C | T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.315+3475G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289553 | ||||||
chr6:106289668 | TA | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(121): Show | 128 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.315+3359delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289668 | ||||||
chr6:106289884 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.315+3144T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106289884 | ||||||
chr6:106290057 | CTG | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.315+2969_315+2970d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290057 | ||||||
chr6:106290185 | C | T | 1 | a0003c0005t0008g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315+2843G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290185 | ||||||
chr6:106290190 | C | CTTATT | 3 | a0001c0001t0001g0298a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | HG00738.hp2 HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.315+2833_315+2837d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290190 | ||||||
chr6:106290221 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315+2807A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290221 | ||||||
chr6:106290242 | CTATTT | C | 7 | a0001c0001t0001g0309a0001c0003t0002g0011a0001c0003t0002g0012others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+2781_315+2785d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290242 | ||||||
chr6:106290259 | ATTTAT | A | 3 | a0001c0001t0001g0057a0003c0005t0008g0067a0003c0005t0008g0068 | 3 | HG02145.hp1 HG02257.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.315+2764_315+2768d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290259 | ||||||
chr6:106290259 | ATTTATTT others(3): Show |
A | 24 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(21): Show | 25 | HG00323.hp1 HG00735.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+2759_315+2768d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290259 | ||||||
chr6:106290372 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+2656C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290372 | ||||||
chr6:106290426 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315+2602A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290426 | ||||||
chr6:106290754 | C | A | 5 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(2): Show | 5 | HG00609.hp2 HG02083.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+2274G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290754 | ||||||
chr6:106290848 | G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 237 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.315+2180C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106290848 | ||||||
chr6:106291438 | C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.315+1590G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291438 | ||||||
chr6:106291489 | A | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.315+1539T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291489 | ||||||
chr6:106291500 | C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+1528G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291500 | ||||||
chr6:106291541 | C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 57 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.315+1487G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291541 | ||||||
chr6:106291590 | C | CTATGA | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.315+1437_315+1438i others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291590 | ||||||
chr6:106291707 | C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.315+1321G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291707 | ||||||
chr6:106291902 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.315+1126A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291902 | ||||||
chr6:106291996 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315+1032G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106291996 | ||||||
chr6:106292272 | G | A | 5 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0292others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+756C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292272 | ||||||
chr6:106292289 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.315+739T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292289 | ||||||
chr6:106292397 | A | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.315+631T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292397 | ||||||
chr6:106292414 | C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02040.hp2 NA18952.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+614G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292414 | ||||||
chr6:106292500 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.315+528G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292500 | ||||||
chr6:106292523 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.315+505T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292523 | ||||||
chr6:106292550 | A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0294 | 3 | NA18979.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.315+478T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292550 | ||||||
chr6:106292583 | A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 237 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.315+445T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292583 | ||||||
chr6:106292749 | C | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+279G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292749 | ||||||
chr6:106292753 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.315+275T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292753 | ||||||
chr6:106292763 | G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.315+265C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292763 | ||||||
chr6:106292778 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.315+250G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292778 | ||||||
chr6:106292884 | T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18977.hp2 NA19001.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.315+144A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292884 | ||||||
chr6:106292889 | A | T | 1 | a0001c0001t0001g0339 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.315+139T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 4/7 | chr6 | 106292889 | ||||||
chr6:106293130 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.237-24C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293130 | ||||||
chr6:106293187 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.237-81A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293187 | ||||||
chr6:106293375 | A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0142a0001c0001t0001g0144 | 3 | HG02165.hp1 NA18960.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.237-269T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293375 | ||||||
chr6:106293406 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.237-300A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293406 | ||||||
chr6:106293575 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.237-469G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293575 | ||||||
chr6:106293583 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-477C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293583 | ||||||
chr6:106293588 | C | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.237-482G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293588 | ||||||
chr6:106293746 | A | G | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-640T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293746 | ||||||
chr6:106293788 | C | G | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-682G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293788 | ||||||
chr6:106293819 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.237-713A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293819 | ||||||
chr6:106293824 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-718A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293824 | ||||||
chr6:106293886 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.237-780A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293886 | ||||||
chr6:106293912 | G | A | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.237-806C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293912 | ||||||
chr6:106293944 | TAG | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.237-840_237-839del others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106293944 | ||||||
chr6:106294078 | G | A | 1 | a0001c0001t0001g0006 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.237-972C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294078 | ||||||
chr6:106294125 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.237-1019A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294125 | ||||||
chr6:106294186 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.237-1080A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294186 | ||||||
chr6:106294213 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.237-1107A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294213 | ||||||
chr6:106294330 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237-1224A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294330 | ||||||
chr6:106294421 | T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-1315A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294421 | ||||||
chr6:106294579 | G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.237-1473C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294579 | ||||||
chr6:106294670 | C | T | 7 | a0001c0001t0001g0249a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-1564G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294670 | ||||||
chr6:106294679 | C | CA | 43 | a0001c0001t0001g0069a0001c0001t0001g0144a0001c0001t0001g0247others(40): Show | 43 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.237-1574dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294679 | ||||||
chr6:106294824 | C | T | 35 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(32): Show | 35 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.237-1718G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294824 | ||||||
chr6:106294845 | G | GA | 9 | a0001c0001t0001g0023a0001c0001t0001g0154a0001c0001t0001g0203others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-1740dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294845 | ||||||
chr6:106294845 | G | GAAAAAAA others(4): Show |
9 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0261others(6): Show | 9 | HG00673.hp1 HG01516.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-1750_237-1740d others(13): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294845 | ||||||
chr6:106294845 | G | GAAAAAAA others(5): Show |
34 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(31): Show | 34 | HG00621.hp2 HG00639.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.237-1751_237-1740d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294845 | ||||||
chr6:106294845 | G | GAAAAAAA others(6): Show |
3 | a0001c0001t0001g0106a0001c0003t0002g0014a0003c0005t0008g0068 | 3 | HG02145.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.237-1752_237-1740d others(15): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106294845 | ||||||
chr6:106295055 | A | T | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 63 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.237-1949T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295055 | ||||||
chr6:106295056 | AT | A | 26 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(23): Show | 26 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-1951delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295056 | ||||||
chr6:106295063 | T | TAC | 6 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01496.hp1 HG02165.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-1959_237-1958d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295063 | ||||||
chr6:106295090 | A | G | 1 | a0001c0001t0005g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-1984T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295090 | ||||||
chr6:106295096 | T | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0145a0001c0001t0001g0171others(1): Show | 4 | HG02602.hp1 HG03017.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-1990A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295096 | ||||||
chr6:106295260 | A | G | 8 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 9 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-2154T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295260 | ||||||
chr6:106295396 | T | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.237-2290A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295396 | ||||||
chr6:106295564 | A | AT | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0084others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.237-2459dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295564 | ||||||
chr6:106295564 | AT | A | 12 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0001g0157others(9): Show | 12 | HG00140.hp2 HG00408.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-2459delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295564 | ||||||
chr6:106295666 | C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0171 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.237-2560G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295666 | ||||||
chr6:106295685 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.237-2579A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295685 | ||||||
chr6:106295924 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.237-2818A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106295924 | ||||||
chr6:106296056 | A | G | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.237-2950T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296056 | ||||||
chr6:106296067 | C | G | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.237-2961G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296067 | ||||||
chr6:106296319 | G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0145a0001c0001t0001g0171others(1): Show | 4 | HG02602.hp1 HG03017.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-3213C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296319 | ||||||
chr6:106296436 | T | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.237-3330A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296436 | ||||||
chr6:106296495 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.237-3389C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296495 | ||||||
chr6:106296540 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.237-3434C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296540 | ||||||
chr6:106296558 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.237-3452G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296558 | ||||||
chr6:106296572 | C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG00738.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.237-3466G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296572 | ||||||
chr6:106296854 | A | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0145a0001c0001t0001g0171others(1): Show | 4 | HG02602.hp1 HG03017.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-3748T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296854 | ||||||
chr6:106296947 | T | C | 2 | a0001c0004t0002g0015a0001c0004t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.237-3841A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106296947 | ||||||
chr6:106297286 | A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(119): Show | 126 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.237-4180T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297286 | ||||||
chr6:106297388 | T | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0121 | 2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.237-4282A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297388 | ||||||
chr6:106297511 | T | G | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-4405A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297511 | ||||||
chr6:106297679 | TTATTC | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02040.hp2 NA18952.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-4578_237-4574d others(7): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297679 | ||||||
chr6:106297717 | A | AAC | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0077others(35): Show | 40 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.237-4613_237-4612d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | A | AACAC | 18 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0070others(15): Show | 18 | HG01516.hp1 HG02056.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.237-4615_237-4612d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | A | AACACAC | 9 | a0001c0001t0001g0073a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG00140.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-4617_237-4612d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0123 | 3 | HG03209.hp2 HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.237-4619_237-4612d others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AAC | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0069others(30): Show | 34 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-4613_237-4612d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACAC | A | 24 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0146others(21): Show | 24 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.237-4615_237-4612d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACAC | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0099others(21): Show | 26 | HG00438.hp1 HG02132.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.237-4617_237-4612d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACACA others(1): Show |
A | 21 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0214others(18): Show | 22 | HG00558.hp1 HG02083.hp1 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.237-4619_237-4612d others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACACA others(3): Show |
A | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0177others(2): Show | 5 | HG02155.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-4621_237-4612d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACACA others(5): Show |
A | 5 | a0001c0001t0001g0225a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG01496.hp2 HG01943.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-4623_237-4612d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACACA others(7): Show |
A | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.237-4625_237-4612d others(16): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297717 | AACACACA others(13): Show |
A | 2 | a0001c0001t0001g0292a0001c0001t0001g0296 | 2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-4631_237-4612d others(22): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297717 | ||||||
chr6:106297747 | CACACACA others(13): Show |
C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-4661_237-4642d others(22): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297747 | ||||||
chr6:106297753 | CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0024 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.237-4661_237-4648d others(16): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297753 | ||||||
chr6:106297755 | CACACACA others(5): Show |
C | 30 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 33 | HG00408.hp2 HG00438.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.237-4661_237-4650d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297755 | ||||||
chr6:106297757 | CACACACA others(3): Show |
C | 19 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0023others(16): Show | 20 | HG00140.hp1 HG02040.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-4661_237-4652d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297757 | ||||||
chr6:106297765 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.237-4659G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297765 | ||||||
chr6:106297767 | T | C | 3 | a0001c0001t0001g0073a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG04228.hp1 NA18978.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.237-4661A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297767 | ||||||
chr6:106297771 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.237-4665A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297771 | ||||||
chr6:106297779 | A | G | 1 | a0001c0001t0001g0337 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.237-4673T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297779 | ||||||
chr6:106297965 | A | AT | 48 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 49 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.237-4860dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297965 | ||||||
chr6:106297965 | AT | A | 19 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0112others(16): Show | 19 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-4860delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106297965 | ||||||
chr6:106298027 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.237-4921G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298027 | ||||||
chr6:106298042 | A | G | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.237-4936T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298042 | ||||||
chr6:106298044 | A | C | 1 | a0001c0001t0006g0002 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.237-4938T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298044 | ||||||
chr6:106298068 | G | A | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.237-4962C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298068 | ||||||
chr6:106298174 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-5068A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298174 | ||||||
chr6:106298188 | T | A | 1 | a0001c0001t0005g0336 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.237-5082A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298188 | ||||||
chr6:106298215 | T | A | 1 | a0001c0003t0002g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237-5109A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298215 | ||||||
chr6:106298280 | A | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | NA18967.hp2 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-5174T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298280 | ||||||
chr6:106298320 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-5214C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298320 | ||||||
chr6:106298407 | T | A | 1 | a0001c0001t0001g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.237-5301A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298407 | ||||||
chr6:106298412 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.237-5306C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298412 | ||||||
chr6:106298429 | T | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.237-5323A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298429 | ||||||
chr6:106298464 | T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0296 | 2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.237-5358A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298464 | ||||||
chr6:106298476 | G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0188 | 2 | HG02056.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.237-5370C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298476 | ||||||
chr6:106298558 | AAAAT | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.237-5456_237-5453d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298558 | ||||||
chr6:106298714 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.237-5608C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298714 | ||||||
chr6:106298847 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.237-5741T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298847 | ||||||
chr6:106298936 | T | C | 3 | a0001c0001t0005g0333a0001c0001t0005g0335a0001c0001t0005g0336 | 3 | HG02970.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.237-5830A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298936 | ||||||
chr6:106298960 | T | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.237-5854A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106298960 | ||||||
chr6:106299119 | G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.237-6013C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299119 | ||||||
chr6:106299190 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.237-6084G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299190 | ||||||
chr6:106299256 | T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-6150A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299256 | ||||||
chr6:106299289 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-6183T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299289 | ||||||
chr6:106299297 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.237-6191G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299297 | ||||||
chr6:106299528 | T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0226 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.237-6422A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299528 | ||||||
chr6:106299610 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.237-6504G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299610 | ||||||
chr6:106299631 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.237-6525A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299631 | ||||||
chr6:106299680 | A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.237-6574T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299680 | ||||||
chr6:106299716 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237-6610C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299716 | ||||||
chr6:106299876 | C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.237-6770G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299876 | ||||||
chr6:106299909 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-6803C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106299909 | ||||||
chr6:106300336 | A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.237-7230T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300336 | ||||||
chr6:106300537 | A | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.237-7431T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300537 | ||||||
chr6:106300568 | A | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.237-7462T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300568 | ||||||
chr6:106300705 | G | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.237-7599C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300705 | ||||||
chr6:106300706 | A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0027 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.237-7600T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300706 | ||||||
chr6:106300729 | C | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.237-7623G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106300729 | ||||||
chr6:106301185 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+7179C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301185 | ||||||
chr6:106301192 | G | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.236+7172C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301192 | ||||||
chr6:106301200 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.236+7164A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301200 | ||||||
chr6:106301203 | C | T | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+7161G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301203 | ||||||
chr6:106301433 | G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(19): Show | 23 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.236+6931C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301433 | ||||||
chr6:106301575 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.236+6789G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301575 | ||||||
chr6:106301683 | C | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.236+6681G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301683 | ||||||
chr6:106301914 | G | A | 1 | a0001c0003t0002g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236+6450C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106301914 | ||||||
chr6:106302327 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+6037C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106302327 | ||||||
chr6:106302841 | G | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+5523C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106302841 | ||||||
chr6:106302916 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.236+5448G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106302916 | ||||||
chr6:106303057 | A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0186a0001c0001t0001g0229others(4): Show | 8 | HG02155.hp2 NA18947.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+5307T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106303057 | ||||||
chr6:106303494 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236+4870A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106303494 | ||||||
chr6:106303707 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.236+4657G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106303707 | ||||||
chr6:106303890 | C | G | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.236+4474G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106303890 | ||||||
chr6:106303974 | G | GA | 50 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(47): Show | 50 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.236+4389dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106303974 | ||||||
chr6:106304073 | CA | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.236+4290delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304073 | ||||||
chr6:106304092 | A | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.236+4272T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304092 | ||||||
chr6:106304178 | G | A | 2 | a0001c0001t0001g0251a0003c0005t0008g0068 | 2 | HG02145.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.236+4186C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304178 | ||||||
chr6:106304265 | C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109others(6): Show | 9 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+4099G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304265 | ||||||
chr6:106304409 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.236+3955A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304409 | ||||||
chr6:106304741 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.236+3623C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304741 | ||||||
chr6:106304960 | G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01071.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.236+3404C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106304960 | ||||||
chr6:106305069 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.236+3295G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305069 | ||||||
chr6:106305091 | C | CA | 43 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0075others(40): Show | 44 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.236+3272dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305091 | ||||||
chr6:106305091 | CA | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 112 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.236+3272delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305091 | ||||||
chr6:106305137 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.236+3227G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305137 | ||||||
chr6:106305244 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.236+3120T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305244 | ||||||
chr6:106305373 | A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(225): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.236+2991T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305373 | ||||||
chr6:106305450 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.236+2914A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305450 | ||||||
chr6:106305544 | GTTCT | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+2816_236+2819d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305544 | ||||||
chr6:106305574 | C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(98): Show | 105 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.236+2790G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305574 | ||||||
chr6:106305621 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+2743C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305621 | ||||||
chr6:106305643 | G | A | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.236+2721C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305643 | ||||||
chr6:106305747 | G | A | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+2617C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305747 | ||||||
chr6:106305778 | G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(52): Show | 59 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.236+2586C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305778 | ||||||
chr6:106305780 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.236+2584T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106305780 | ||||||
chr6:106306061 | T | G | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+2303A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306061 | ||||||
chr6:106306272 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.236+2092G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306272 | ||||||
chr6:106306494 | T | C | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236+1870A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306494 | ||||||
chr6:106306554 | A | G | 19 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+1810T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306554 | ||||||
chr6:106306584 | T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.236+1780A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306584 | ||||||
chr6:106306629 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.236+1735G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306629 | ||||||
chr6:106306753 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.236+1611G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306753 | ||||||
chr6:106306808 | CCTTT | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+1552_236+1555d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306808 | ||||||
chr6:106306835 | T | C | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.236+1529A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306835 | ||||||
chr6:106306892 | G | T | 3 | a0001c0001t0001g0252a0003c0005t0008g0067a0003c0005t0008g0068 | 3 | HG01123.hp1 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.236+1472C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306892 | ||||||
chr6:106306980 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.236+1384A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106306980 | ||||||
chr6:106307019 | T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0113 | 3 | HG00099.hp1 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.236+1345A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307019 | ||||||
chr6:106307034 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.236+1330G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307034 | ||||||
chr6:106307244 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.236+1120G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307244 | ||||||
chr6:106307347 | A | G | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.236+1017T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307347 | ||||||
chr6:106307534 | CCTT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(46): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.236+827_236+829del others(3): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307534 | ||||||
chr6:106307535 | C | CT | 47 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(44): Show | 47 | HG00609.hp2 HG00673.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.236+828dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307535 | ||||||
chr6:106307535 | CT | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0070others(59): Show | 62 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.236+828delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307535 | ||||||
chr6:106307535 | CTT | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0005g0334others(5): Show | 8 | HG01169.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+827_236+828del others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307535 | ||||||
chr6:106307720 | G | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+644C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307720 | ||||||
chr6:106307920 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+444G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106307920 | ||||||
chr6:106308043 | GAAT | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+318_236+320del others(3): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106308043 | ||||||
chr6:106308157 | A | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+207T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 3/7 | chr6 | 106308157 | ||||||
chr6:106308882 | C | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.109-391G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106308882 | ||||||
chr6:106308936 | A | G | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-445T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106308936 | ||||||
chr6:106309065 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.109-574T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309065 | ||||||
chr6:106309144 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109-653A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309144 | ||||||
chr6:106309157 | C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG00741.hp2 HG01169.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-666G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309157 | ||||||
chr6:106309242 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.109-751G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309242 | ||||||
chr6:106309406 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.109-915G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309406 | ||||||
chr6:106309539 | A | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(225): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.109-1048T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309539 | ||||||
chr6:106309615 | G | GC | 12 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(9): Show | 12 | HG00621.hp2 HG00673.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.109-1125_109-1124i others(3): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309615 | ||||||
chr6:106309620 | T | C | 12 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(9): Show | 12 | HG00621.hp2 HG00673.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.109-1129A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309620 | ||||||
chr6:106309633 | G | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-1142C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309633 | ||||||
chr6:106309639 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.109-1148A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309639 | ||||||
chr6:106309641 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.109-1150C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309641 | ||||||
chr6:106309755 | T | C | 11 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG00741.hp2 HG01169.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-1264A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309755 | ||||||
chr6:106309833 | T | A | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-1342A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309833 | ||||||
chr6:106309842 | C | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-1351G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106309842 | ||||||
chr6:106310244 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.109-1753A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106310244 | ||||||
chr6:106310470 | T | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(34): Show | 37 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.109-1979A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106310470 | ||||||
chr6:106310691 | C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG00738.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.109-2200G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106310691 | ||||||
chr6:106310897 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-2406G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106310897 | ||||||
chr6:106310947 | G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18978.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.109-2456C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106310947 | ||||||
chr6:106311076 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.109-2585A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311076 | ||||||
chr6:106311219 | A | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.109-2728T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311219 | ||||||
chr6:106311307 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.109-2816A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311307 | ||||||
chr6:106311832 | C | CT | 50 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(47): Show | 50 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.109-3342dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311832 | ||||||
chr6:106311941 | C | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-3450G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311941 | ||||||
chr6:106311957 | G | A | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-3466C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106311957 | ||||||
chr6:106312122 | T | C | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.109-3631A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312122 | ||||||
chr6:106312173 | G | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.109-3682C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312173 | ||||||
chr6:106312222 | G | A | 44 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(41): Show | 44 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.109-3731C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312222 | ||||||
chr6:106312227 | T | A | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.109-3736A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312227 | ||||||
chr6:106312235 | T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.109-3744A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312235 | ||||||
chr6:106312271 | G | A | 4 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-3780C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312271 | ||||||
chr6:106312274 | G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00408.hp1 NA18950.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-3783C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312274 | ||||||
chr6:106312424 | A | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01071.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.108+3677T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312424 | ||||||
chr6:106312553 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.108+3548T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312553 | ||||||
chr6:106312623 | T | TAC | 12 | a0001c0001t0001g0109a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 12 | HG00639.hp2 HG02040.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.108+3476_108+3477d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | T | TACACAC | 5 | a0001c0001t0001g0117a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG00140.hp2 HG01106.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+3472_108+3477d others(8): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.108+3470_108+3477d others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0093 | 2 | HG02273.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.108+3468_108+3477d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | TAC | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084others(13): Show | 16 | HG02056.hp2 HG02622.hp1 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.108+3476_108+3477d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | TACAC | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 89 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.108+3474_108+3477d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(11): Show | 14 | HG01175.hp1 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+3470_108+3477d others(10): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | TACACACA others(3): Show |
T | 2 | a0001c0001t0005g0333a0001c0001t0005g0334 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108+3468_108+3477d others(12): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312623 | TACACACA others(5): Show |
T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(82): Show | 89 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.108+3466_108+3477d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312623 | ||||||
chr6:106312639 | C | T | 12 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01175.hp1 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.108+3462G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312639 | ||||||
chr6:106312643 | C | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+3458G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312643 | ||||||
chr6:106312693 | A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0189 | 2 | NA18967.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.108+3408T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312693 | ||||||
chr6:106312710 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.108+3391C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312710 | ||||||
chr6:106312719 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.108+3382T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312719 | ||||||
chr6:106312722 | A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(176): Show | 186 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.108+3379T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312722 | ||||||
chr6:106312723 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.108+3378A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312723 | ||||||
chr6:106312733 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108+3368A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312733 | ||||||
chr6:106312751 | A | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.108+3350T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312751 | ||||||
chr6:106312798 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+3303A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312798 | ||||||
chr6:106312886 | C | A | 1 | a0001c0001t0001g0288 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.108+3215G>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312886 | ||||||
chr6:106312902 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.108+3199C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312902 | ||||||
chr6:106312983 | A | G | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+3118T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106312983 | ||||||
chr6:106313050 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.108+3051C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313050 | ||||||
chr6:106313093 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+3008C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313093 | ||||||
chr6:106313137 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+2964C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313137 | ||||||
chr6:106313302 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108+2799C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313302 | ||||||
chr6:106313764 | ATAT | A | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+2334_108+2336d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313764 | ||||||
chr6:106313860 | G | A | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.108+2241C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313860 | ||||||
chr6:106313890 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.108+2211A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106313890 | ||||||
chr6:106314243 | T | C | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.108+1858A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314243 | ||||||
chr6:106314294 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.108+1807A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314294 | ||||||
chr6:106314414 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.108+1687C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314414 | ||||||
chr6:106314492 | G | A | 46 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(43): Show | 46 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.108+1609C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314492 | ||||||
chr6:106314622 | C | T | 38 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(35): Show | 38 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.108+1479G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314622 | ||||||
chr6:106314719 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+1382C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314719 | ||||||
chr6:106314734 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.108+1367T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314734 | ||||||
chr6:106314926 | C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0007g0205 | 3 | HG01516.hp1 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.108+1175G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106314926 | ||||||
chr6:106315097 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108+1004A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315097 | ||||||
chr6:106315205 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+896C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315205 | ||||||
chr6:106315224 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.108+877T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315224 | ||||||
chr6:106315423 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108+678C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315423 | ||||||
chr6:106315781 | T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(49): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.108+320A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315781 | ||||||
chr6:106315815 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.108+286C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315815 | ||||||
chr6:106315835 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+266A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315835 | ||||||
chr6:106315867 | A | C | 1 | a0003c0005t0008g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.108+234T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315867 | ||||||
chr6:106315970 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.108+131T>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 2/7 | chr6 | 106315970 | ||||||
chr6:106316374 | CA | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0078others(6): Show | 10 | HG00323.hp1 HG00735.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58-109delT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316374 | ||||||
chr6:106316456 | C | T | 46 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(43): Show | 46 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-58-190G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316456 | ||||||
chr6:106316486 | T | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58-220A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316486 | ||||||
chr6:106316503 | T | C | 1 | a0001c0001t0005g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-58-237A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316503 | ||||||
chr6:106316541 | T | C | 1 | a0001c0001t0004g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-58-275A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316541 | ||||||
chr6:106316598 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-58-332A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316598 | ||||||
chr6:106316982 | C | T | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-58-716G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316982 | ||||||
chr6:106316991 | G | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 134 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-58-725C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106316991 | ||||||
chr6:106317263 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-58-997A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106317263 | ||||||
chr6:106317341 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-58-1075T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106317341 | ||||||
chr6:106317570 | TGGTTATT others(7): Show |
T | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-58-1318_-58-1305d others(16): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106317570 | ||||||
chr6:106318170 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-58-1904T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318170 | ||||||
chr6:106318204 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-58-1938A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318204 | ||||||
chr6:106318254 | G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(225): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.-58-1988C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318254 | ||||||
chr6:106318283 | G | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58-2017C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318283 | ||||||
chr6:106318504 | T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58-2238A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318504 | ||||||
chr6:106318507 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58-2241G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318507 | ||||||
chr6:106318602 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-58-2336A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106318602 | ||||||
chr6:106319038 | A | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58-2772T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319038 | ||||||
chr6:106319060 | T | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0176others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58-2794A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319060 | ||||||
chr6:106319061 | A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(176): Show | 186 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-58-2795T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319061 | ||||||
chr6:106319080 | A | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-58-2814T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319080 | ||||||
chr6:106319082 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58-2816G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319082 | ||||||
chr6:106319099 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-58-2833A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319099 | ||||||
chr6:106319266 | C | T | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58-3000G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319266 | ||||||
chr6:106319293 | A | C | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58-3027T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319293 | ||||||
chr6:106319332 | A | AT | 44 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0101others(41): Show | 44 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58-3067dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319332 | ||||||
chr6:106319400 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58-3134C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319400 | ||||||
chr6:106319438 | G | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0297 | 3 | HG02622.hp1 HG02683.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-58-3172C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319438 | ||||||
chr6:106319701 | T | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(100): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-58-3435A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319701 | ||||||
chr6:106319705 | C | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0176 | 3 | HG00642.hp1 HG02258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-58-3439G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319705 | ||||||
chr6:106319752 | C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(48): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-58-3486G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319752 | ||||||
chr6:106319913 | T | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-58-3647A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319913 | ||||||
chr6:106319932 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-58-3666A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106319932 | ||||||
chr6:106320001 | T | C | 2 | a0003c0005t0008g0067a0003c0005t0008g0068 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-58-3735A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106320001 | ||||||
chr6:106320143 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-3877A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106320143 | ||||||
chr6:106320294 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-58-4028C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106320294 | ||||||
chr6:106320625 | G | GA | 152 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 155 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.-58-4360dupT | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106320625 | ||||||
chr6:106321210 | A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0113 | 3 | HG00099.hp1 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-59+4316T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321210 | ||||||
chr6:106321362 | C | CT | 17 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0107others(14): Show | 17 | HG00558.hp1 HG00621.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-59+4163dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321362 | ||||||
chr6:106321363 | T | C | 45 | a0001c0001t0001g0069a0001c0001t0001g0247a0001c0001t0001g0249others(42): Show | 45 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-59+4163A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321363 | ||||||
chr6:106321507 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-59+4019G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321507 | ||||||
chr6:106321513 | C | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG00438.hp1 HG02155.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.-59+4013G>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321513 | ||||||
chr6:106321552 | ATTTCACC others(1572): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-59+2395_-59+3973d others(2): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321552 | ||||||
chr6:106321643 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-59+3883G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321643 | ||||||
chr6:106321648 | G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01071.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-59+3878C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321648 | ||||||
chr6:106321677 | T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-59+3849A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321677 | ||||||
chr6:106321681 | G | A | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-59+3845C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321681 | ||||||
chr6:106321745 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-59+3781A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321745 | ||||||
chr6:106321767 | T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 245 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.-59+3759A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321767 | ||||||
chr6:106321969 | ACTC | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 8 | HG00438.hp2 NA18612.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.-59+3554_-59+3556d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106321969 | ||||||
chr6:106322086 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-59+3440A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322086 | ||||||
chr6:106322113 | T | G | 1 | a0001c0001t0001g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-59+3413A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322113 | ||||||
chr6:106322214 | CCAA | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-59+3309_-59+3311d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322214 | ||||||
chr6:106322286 | T | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG00408.hp1 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-59+3240A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322286 | ||||||
chr6:106322680 | A | G | 5 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01891.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+2846T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322680 | ||||||
chr6:106322685 | G | A | 5 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01891.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+2841C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322685 | ||||||
chr6:106322793 | T | C | 36 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(33): Show | 36 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-59+2733A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322793 | ||||||
chr6:106322938 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-59+2588C>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322938 | ||||||
chr6:106322951 | GCT | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0193a0001c0001t0001g0194others(11): Show | 14 | HG01109.hp2 HG02132.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.-59+2573_-59+2574d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322951 | ||||||
chr6:106322994 | T | A | 3 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280 | 3 | NA18946.hp1 NA18981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-59+2532A>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106322994 | ||||||
chr6:106323080 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-59+2446C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323080 | ||||||
chr6:106323104 | T | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0010g0284 | 3 | HG00642.hp2 HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-59+2422A>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323104 | ||||||
chr6:106323113 | A | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-59+2413T>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323113 | ||||||
chr6:106323127 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-59+2399G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323127 | ||||||
chr6:106323253 | A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | NA18979.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-59+2273T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323253 | ||||||
chr6:106323260 | C | CT | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-59+2265dupA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323260 | ||||||
chr6:106323260 | C | CTT | 36 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0077others(33): Show | 36 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-59+2264_-59+2265d others(4): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323260 | ||||||
chr6:106323260 | C | CTTT | 7 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0073others(4): Show | 7 | HG02602.hp2 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-59+2263_-59+2265d others(5): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323260 | ||||||
chr6:106323260 | CT | C | 60 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-59+2265delA | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323260 | ||||||
chr6:106323287 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-59+2239T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323287 | ||||||
chr6:106323350 | C | T | 1 | a0003c0005t0008g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-59+2176G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323350 | ||||||
chr6:106323431 | T | C | 4 | a0001c0001t0005g0333a0001c0001t0005g0334a0001c0001t0005g0335others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-59+2095A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323431 | ||||||
chr6:106323438 | CTAAT | C | 6 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(3): Show | 6 | HG00609.hp2 HG02083.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-59+2084_-59+2087d others(6): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323438 | ||||||
chr6:106323506 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-59+2020A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323506 | ||||||
chr6:106323523 | G | C | 1 | a0001c0001t0001g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-59+2003C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323523 | ||||||
chr6:106323538 | C | CAAGTTAT others(5): Show |
1 | a0001c0001t0001g0070 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-59+1976_-59+1987d others(14): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323538 | ||||||
chr6:106323657 | ACCCTGAT others(22): Show |
A | 1 | a0001c0001t0001g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-59+1840_-59+1868d others(31): Show |
ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323657 | ||||||
chr6:106323690 | G | C | 1 | a0001c0001t0001g0345 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-59+1836C>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323690 | ||||||
chr6:106323718 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-59+1808T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323718 | ||||||
chr6:106323967 | C | T | 7 | a0001c0001t0012g0019a0001c0003t0002g0011a0001c0003t0002g0012others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-59+1559G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106323967 | ||||||
chr6:106324002 | G | A | 1 | a0001c0001t0004g0346 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-59+1524C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106324002 | ||||||
chr6:106324131 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-59+1395A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106324131 | ||||||
chr6:106324898 | C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(47): Show | 54 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-59+628G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106324898 | ||||||
chr6:106324994 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-59+532C>T | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106324994 | ||||||
chr6:106325137 | T | C | 1 | a0001c0001t0012g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-59+389A>G | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106325137 | ||||||
chr6:106325293 | A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0012g0019 | 3 | HG02622.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-59+233T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106325293 | ||||||
chr6:106325429 | C | T | 6 | a0001c0003t0002g0011a0001c0003t0002g0012a0001c0003t0002g0013others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-59+97G>A | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106325429 | ||||||
chr6:106325460 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-59+66T>C | ATG5 | ENSG00000057663.16 | transcript | ENST00000369076.8 | protein_coding | 1/7 | chr6 | 106325460 |