geneid | 27244 |
---|---|
ensemblid | ENSG00000080546.14 |
hgncid | 21595 |
symbol | SESN1 |
name | sestrin 1 |
refseq_nuc | NM_014454.3 |
refseq_prot | NP_055269.1 |
ensembl_nuc | ENST00000436639.7 |
ensembl_prot | ENSP00000393762.2 |
mane_status | MANE Select |
chr | chr6 |
start | 108984309 |
end | 109094846 |
strand | - |
ver | v1.2 |
region | chr6:108984309-109094846 |
region5000 | chr6:108979309-109099846 |
regionname0 | SESN1_chr6_108984309_109094846 |
regionname5000 | SESN1_chr6_108979309_109099846 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 551 | 155 | 62 | 26 | 40 | 5 | 20 | 29 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0002 | 0/0 | 551 | 26 | 1 | 6 | 8 | 3 | 8 | 7 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0003 | 0/0 | 550 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0004 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1656 | 143 | 54 | 24 | 38 | 5 | 20 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0002 | 0/0 | 1656 | 26 | 1 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0003 | 0/0 | 1656 | 6 | 6 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0004 | 0/0 | 1656 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0005 | 0/0 | 1656 | 2 | 0 | 0 | 2 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
c0007 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 4009 | 113 | 38 | 20 | 32 | 5 | 16 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0002 | 0/0 | 4005 | 27 | 2 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0003 | 0/0 | 4013 | 18 | 8 | 2 | 6 | 0 | 2 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0004 | 0/0 | 4009 | 5 | 5 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0005 | 0/0 | 4013 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0006 | 0/0 | 4009 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0007 | 0/0 | 4009 | 3 | 0 | 2 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0008 | 0/0 | 4009 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0009 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0010 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0011 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0012 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0013 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0014 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0015 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
t0016 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1656 | 143 | 54 | 24 | 38 | 5 | 20 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0003 | 0/0 | 1656 | 6 | 6 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0004 | 0/0 | 1656 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0005 | 0/0 | 1656 | 2 | 0 | 0 | 2 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0002c0002 | 0/0 | 1656 | 26 | 1 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0003c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0004c0007 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5664 | 108 | 35 | 20 | 30 | 5 | 16 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0003 | 0/0 | 5668 | 18 | 8 | 2 | 6 | 0 | 2 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0006 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0007 | 0/0 | 5664 | 3 | 0 | 2 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0008 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0009 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0010 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0011 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0012 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0013 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0014 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0015 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0001t0016 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0003t0002 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0003t0004 | 0/0 | 5664 | 5 | 5 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0004t0005 | 0/0 | 5668 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0001c0005t0001 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0002c0002t0002 | 0/0 | 5660 | 26 | 1 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0003c0006t0001 | 0/0 | 5661 | 2 | 2 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
a0004c0007t0001 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | copy fasta | chr6 | 108979309 | 109099846 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0015g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0003t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0004t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0004t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0004t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0004t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0001c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0003c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0003c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
a0004c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0031 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0032 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0048 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01168 | hp2 | a0001 | c0004 | t0005 | g0023 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01169 | hp2 | a0001 | c0004 | t0005 | g0022 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02055 | hp1 | a0003 | c0006 | t0001 | g0059 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02280 | hp1 | a0001 | c0001 | t0016 | g0183 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02451 | hp1 | a0001 | c0004 | t0005 | g0020 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0005 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02622 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02630 | hp2 | a0004 | c0007 | t0001 | g0017 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0066 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0015 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02886 | hp1 | a0001 | c0004 | t0005 | g0021 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0182 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03130 | hp2 | a0003 | c0006 | t0001 | g0057 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0004 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03540 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03669 | hp2 | a0001 | c0001 | t0014 | g0158 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | YRI | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0002 | AFR | YRI | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18998 | hp1 | a0001 | c0005 | t0001 | g0009 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19012 | hp1 | a0001 | c0001 | t0015 | g0141 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA19089 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ASW | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ASW | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | GIH | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0089 | REF | REF | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108992887
|
ACTT | A | 1 | a0003 | 2 | HG02055.hp1 HG03130.hp2 |
disruptive_inframe_deletion | MODERATE | c.1130_1132delAAG | p.Glu377del | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/10 | 1905/5664 | 1130/1656 | 377/551 | chr6 | 108992887 | ||
chr6:108998551
|
C | T | 1 | a0004 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.934G>A | p.Val312Met | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/10 | 1707/5664 | 934/1656 | 312/551 | chr6 | 108998551 | ||
chr6:109002316
|
G | T | 1 | a0002 | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
missense_variant | MODERATE | c.307C>A | p.Leu103Ile | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/10 | 1080/5664 | 307/1656 | 103/551 | chr6 | 109002316 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108998567
|
T | C | 1 | a0001c0004 | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
synonymous_variant | LOW | c.918A>G | p.Thr306Thr | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/10 | 1691/5664 | 918/1656 | 306/551 | chr6 | 108998567 | ||
chr6:109001351
|
C | T | 2 | a0001c0003a0002c0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
synonymous_variant | LOW | c.483G>A | p.Gln161Gln | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/10 | 1256/5664 | 483/1656 | 161/551 | chr6 | 109001351 | ||
chr6:109093977
|
A | G | 1 | a0001c0005 | 2 | NA18998.hp1 NA19080.hp2 |
synonymous_variant | LOW | c.97T>C | p.Leu33Leu | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 870/5664 | 97/1656 | 33/551 | chr6 | 109093977 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108984362
|
C | T | 1 | a0001c0001t0012 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 3182 | chr6 | 108984362 | |||||
chr6:108984540
|
T | C | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3004A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 3004 | chr6 | 108984540 | |||||
chr6:108984848
|
T | C | 1 | a0001c0004t0005 | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2696A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2696 | chr6 | 108984848 | |||||
chr6:108984907
|
A | G | 1 | a0001c0001t0007 | 3 | HG01106.hp2 HG01361.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2637T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2637 | chr6 | 108984907 | |||||
chr6:108984962
|
G | A | 1 | a0001c0001t0013 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2582 | chr6 | 108984962 | |||||
chr6:108985143
|
T | C | 1 | a0001c0001t0014 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2401 | chr6 | 108985143 | |||||
chr6:108985198
|
T | G | 1 | a0001c0001t0015 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2346A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2346 | chr6 | 108985198 | |||||
chr6:108985277
|
C | T | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2267G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2267 | chr6 | 108985277 | |||||
chr6:108985286
|
C | A | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2258G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2258 | chr6 | 108985286 | |||||
chr6:108985290
|
T | G | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2254A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2254 | chr6 | 108985290 | |||||
chr6:108985291
|
CA | C | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2252delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2252 | chr6 | 108985291 | |||||
chr6:108985478
|
T | C | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2066A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2066 | chr6 | 108985478 | |||||
chr6:108985760
|
C | A | 2 | a0001c0003t0002a0002c0002t0002 | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1784G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1784 | chr6 | 108985760 | |||||
chr6:108985773
|
A | T | 1 | a0001c0001t0011 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1771T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1771 | chr6 | 108985773 | |||||
chr6:108986078
|
TATC | T | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1463_*1465delGAT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1463 | chr6 | 108986078 | |||||
chr6:108986370
|
G | GTAGA | 3 | a0001c0001t0003a0001c0003t0004a0001c0004t0005 | 27 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1170_*1173dupTCTA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1173 | chr6 | 108986370 | |||||
chr6:108986507
|
G | A | 3 | a0001c0003t0002a0001c0003t0004a0002c0002t0002 | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1037 | chr6 | 108986507 | |||||
chr6:108986684
|
C | T | 1 | a0001c0001t0010 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 860 | chr6 | 108986684 | |||||
chr6:108986703
|
C | T | 1 | a0001c0001t0006 | 3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 841 | chr6 | 108986703 | |||||
chr6:108987518
|
G | C | 1 | a0001c0001t0008 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 26 | chr6 | 108987518 | |||||
chr6:109094079
|
T | C | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | chr6 | 109094079 | ||||||
chr6:109094312
|
T | G | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-239A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 239 | chr6 | 109094312 | |||||
chr6:109094453
|
C | T | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-380G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 380 | chr6 | 109094453 | |||||
chr6:109094567
|
C | T | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-494G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 494 | chr6 | 109094567 | |||||
chr6:109094662
|
C | A | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-589G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 589 | chr6 | 109094662 | |||||
chr6:109094809
|
C | T | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-736G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 736 | chr6 | 109094809 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:108987647
|
A | G | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1570-17T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987647 | ||||||
chr6:108987749
|
C | A | 33 | a0001c0001t0010g0010a0001c0003t0002g0182a0001c0003t0004g0002others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1570-119G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987749 | ||||||
chr6:108987806
|
C | CTTTT | 24 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1570-180_1570-177d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | ||||||
chr6:108987806
|
C | CTTTTT | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1570-181_1570-177d others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | ||||||
chr6:108987806
|
C | CTTTTTT | 48 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0126others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1570-182_1570-177d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | ||||||
chr6:108987806
|
C | CTTTTTTT | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0003g0167others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1570-183_1570-177d others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | ||||||
chr6:108987905
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1570-275G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987905 | ||||||
chr6:108987947
|
T | C | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1570-317A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987947 | ||||||
chr6:108988050
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0134 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1570-420A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988050 | ||||||
chr6:108988084
|
A | G | 62 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1570-454T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988084 | ||||||
chr6:108988239
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1569+304A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988239 | ||||||
chr6:108988799
|
G | C | 2 | a0001c0004t0005g0020a0001c0004t0005g0021 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1425-112C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108988799 | ||||||
chr6:108988822
|
A | C | 2 | a0001c0001t0001g0126a0001c0001t0013g0015 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1425-135T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108988822 | ||||||
chr6:108989065
|
C | T | 28 | a0001c0001t0010g0010a0001c0003t0002g0182a0002c0002t0002g0013others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1425-378G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989065 | ||||||
chr6:108989070
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1425-383A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989070 | ||||||
chr6:108989222
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1425-535T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989222 | ||||||
chr6:108989391
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1425-704G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989391 | ||||||
chr6:108989393
|
C | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1425-706G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989393 | ||||||
chr6:108989424
|
G | GAT | 27 | a0001c0003t0002g0182a0002c0002t0002g0013a0002c0002t0002g0014others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1425-739_1425-738d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989424 | ||||||
chr6:108989425
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1425-738T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989425 | ||||||
chr6:108989427
|
ATATATCT others(17): Show |
A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1425-764_1425-741d others(26): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989427 | ||||||
chr6:108989428
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1425-741A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989428 | ||||||
chr6:108989446
|
C | T | 60 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1425-759G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989446 | ||||||
chr6:108989454
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1425-767A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989454 | ||||||
chr6:108989454
|
TATCTAGA others(31): Show |
T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0123 | 3 | HG01168.hp1 HG02486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1425-805_1425-768d others(40): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989454 | ||||||
chr6:108989505
|
CTA | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1425-820_1425-819d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989505 | ||||||
chr6:108989516
|
T | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1425-829A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989516 | ||||||
chr6:108989529
|
ATAGAGAT others(31): Show |
A | 55 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1425-880_1425-843d others(40): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989529 | ||||||
chr6:108989546
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1425-859A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989546 | ||||||
chr6:108989567
|
C | A | 1 | a0003c0006t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1425-880G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989567 | ||||||
chr6:108990158
|
G | A | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1424+487C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990158 | ||||||
chr6:108990224
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1424+421C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990224 | ||||||
chr6:108990357
|
T | G | 55 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1424+288A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990357 | ||||||
chr6:108990483
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1424+162C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990483 | ||||||
chr6:108990529
|
T | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | NA19012.hp2 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1424+116A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990529 | ||||||
chr6:108990561
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1424+84C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990561 | ||||||
chr6:108991021
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1234-186A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991021 | ||||||
chr6:108991036
|
C | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-201G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991036 | ||||||
chr6:108991066
|
C | CA | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-232dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991066 | ||||||
chr6:108991073
|
A | AAAC | 25 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(22): Show | 25 | HG01109.hp1 HG01891.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.1234-241_1234-239d others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991073 | ||||||
chr6:108991073
|
A | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(65): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1234-238T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991073 | ||||||
chr6:108991074
|
AAC | A | 21 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0026others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1234-241_1234-240d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991074 | ||||||
chr6:108991075
|
AC | A | 4 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0043others(1): Show | 4 | HG00438.hp1 HG01175.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-241delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991075 | ||||||
chr6:108991076
|
C | A | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-241G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991076 | ||||||
chr6:108991079
|
C | A | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-244G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991079 | ||||||
chr6:108991082
|
C | A | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-247G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991082 | ||||||
chr6:108991082
|
C | CAAA | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-250_1234-248d others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991082 | ||||||
chr6:108991085
|
A | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1234-250T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991085 | ||||||
chr6:108991228
|
A | AGT | 11 | a0001c0001t0001g0088a0001c0001t0001g0117a0001c0001t0001g0118others(8): Show | 11 | HG00280.hp1 HG01168.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-395_1234-394d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | ||||||
chr6:108991228
|
AGT | A | 9 | a0001c0001t0001g0179a0001c0001t0003g0135a0001c0001t0003g0159others(6): Show | 9 | HG01891.hp2 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-395_1234-394d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | ||||||
chr6:108991228
|
AGTGT | A | 47 | a0001c0001t0001g0126a0001c0001t0003g0131a0001c0001t0003g0161others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1234-397_1234-394d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | ||||||
chr6:108991228
|
AGTGTGT | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1234-399_1234-394d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | ||||||
chr6:108991295
|
A | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-460T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991295 | ||||||
chr6:108991486
|
C | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-651G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991486 | ||||||
chr6:108991830
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1233+957G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991830 | ||||||
chr6:108992068
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1233+719T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992068 | ||||||
chr6:108992100
|
C | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1233+687G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992100 | ||||||
chr6:108992291
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1233+496A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992291 | ||||||
chr6:108992308
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1233+479C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992308 | ||||||
chr6:108992397
|
G | A | 3 | a0001c0001t0006g0070a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1233+390C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992397 | ||||||
chr6:108992426
|
T | C | 33 | a0001c0001t0010g0010a0001c0003t0002g0182a0001c0003t0004g0002others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1233+361A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992426 | ||||||
chr6:108992525
|
C | T | 65 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1233+262G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992525 | ||||||
chr6:108993147
|
T | C | 65 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1121-248A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993147 | ||||||
chr6:108993190
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-291C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993190 | ||||||
chr6:108993272
|
AGATT | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG02280.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121-377_1121-374d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993272 | ||||||
chr6:108993753
|
G | GT | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+708dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993753 | ||||||
chr6:108993788
|
C | A | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1120+674G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993788 | ||||||
chr6:108993828
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+634G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993828 | ||||||
chr6:108993906
|
C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1120+556G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993906 | ||||||
chr6:108993912
|
T | C | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1120+550A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993912 | ||||||
chr6:108994018
|
T | C | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+444A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994018 | ||||||
chr6:108994078
|
T | G | 16 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(13): Show | 16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1120+384A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994078 | ||||||
chr6:108994096
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1120+366G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994096 | ||||||
chr6:108994140
|
T | TA | 8 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0093others(5): Show | 8 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+321dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994140 | ||||||
chr6:108994140
|
TA | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0073others(12): Show | 15 | HG00323.hp2 HG01168.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1120+321delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994140 | ||||||
chr6:108994163
|
A | AG | 3 | a0002c0002t0002g0029a0002c0002t0002g0041a0002c0002t0002g0044 | 3 | HG01123.hp2 HG02738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1120+298dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994163 | ||||||
chr6:108994163
|
A | G | 29 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+299T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994163 | ||||||
chr6:108994698
|
C | CT | 57 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.973-90dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994698 | ||||||
chr6:108994753
|
A | T | 17 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.973-144T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994753 | ||||||
chr6:108994796
|
A | G | 102 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.973-187T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994796 | ||||||
chr6:108994879
|
T | G | 9 | a0001c0001t0001g0072a0001c0001t0001g0136a0001c0001t0001g0143others(6): Show | 9 | HG02293.hp1 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.973-270A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994879 | ||||||
chr6:108994970
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973-361G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994970 | ||||||
chr6:108995199
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.973-590C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995199 | ||||||
chr6:108995200
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.973-591A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995200 | ||||||
chr6:108995449
|
C | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-840G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995449 | ||||||
chr6:108995471
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.973-862T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995471 | ||||||
chr6:108995551
|
C | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-942G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995551 | ||||||
chr6:108995674
|
G | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0171 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.973-1065C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995674 | ||||||
chr6:108995752
|
C | T | 2 | a0001c0005t0001g0008a0001c0005t0001g0009 | 2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.973-1143G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995752 | ||||||
chr6:108995838
|
AT | A | 27 | a0001c0003t0002g0182a0002c0002t0002g0013a0002c0002t0002g0014others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.973-1230delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995838 | ||||||
chr6:108996024
|
T | C | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.973-1415A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996024 | ||||||
chr6:108996064
|
G | T | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.973-1455C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996064 | ||||||
chr6:108996127
|
C | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1518G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996127 | ||||||
chr6:108996185
|
A | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1576T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996185 | ||||||
chr6:108996191
|
C | G | 34 | a0001c0001t0010g0010a0001c0001t0013g0015a0001c0003t0002g0182others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.973-1582G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996191 | ||||||
chr6:108996432
|
C | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1823G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996432 | ||||||
chr6:108997076
|
G | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1437C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997076 | ||||||
chr6:108997077
|
A | T | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1436T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997077 | ||||||
chr6:108997117
|
A | G | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.972+1396T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997117 | ||||||
chr6:108997132
|
CAA | C | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1379_972+1380d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997132 | ||||||
chr6:108997313
|
G | C | 66 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.972+1200C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997313 | ||||||
chr6:108997501
|
T | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1012A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997501 | ||||||
chr6:108997557
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.972+956C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997557 | ||||||
chr6:108997640
|
A | G | 34 | a0001c0001t0010g0010a0001c0001t0013g0015a0001c0003t0002g0182others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.972+873T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997640 | ||||||
chr6:108997884
|
T | C | 1 | a0001c0001t0006g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.972+629A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997884 | ||||||
chr6:108997995
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.972+518T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997995 | ||||||
chr6:108998104
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+409G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108998104 | ||||||
chr6:108998776
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.730-21C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108998776 | ||||||
chr6:108999238
|
T | C | 34 | a0001c0001t0010g0010a0001c0001t0013g0015a0001c0003t0002g0182others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.730-483A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999238 | ||||||
chr6:108999543
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.730-788A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999543 | ||||||
chr6:108999692
|
T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.729+799A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999692 | ||||||
chr6:108999855
|
C | T | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+636G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999855 | ||||||
chr6:109000128
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0105others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+363A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000128 | ||||||
chr6:109000146
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.729+345C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000146 | ||||||
chr6:109000294
|
G | A | 27 | a0001c0003t0002g0182a0002c0002t0002g0013a0002c0002t0002g0014others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.729+197C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000294 | ||||||
chr6:109000378
|
CA | C | 17 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.729+112delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000378 | ||||||
chr6:109000399
|
T | G | 4 | a0002c0002t0002g0027a0002c0002t0002g0032a0002c0002t0002g0033others(1): Show | 4 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+92A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000399 | ||||||
chr6:109000795
|
C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.547-122G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000795 | ||||||
chr6:109000842
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.547-169C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000842 | ||||||
chr6:109000846
|
G | A | 1 | a0001c0004t0005g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-173C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000846 | ||||||
chr6:109000980
|
A | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.547-307T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000980 | ||||||
chr6:109001163
|
G | C | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.546+125C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109001163 | ||||||
chr6:109001274
|
G | C | 27 | a0001c0003t0002g0182a0002c0002t0002g0013a0002c0002t0002g0014others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.546+14C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109001274 | ||||||
chr6:109001498
|
T | TGA | 33 | a0001c0001t0010g0010a0001c0003t0002g0182a0001c0003t0004g0002others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.346-12_346-11dupTC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001498 | ||||||
chr6:109001751
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346-263T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001751 | ||||||
chr6:109001929
|
TC | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+348delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001929 | ||||||
chr6:109002016
|
ATGT | A | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.345+259_345+261del others(3): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109002016 | ||||||
chr6:109002378
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280-35C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109002378 | ||||||
chr6:109002720
|
G | A | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-377C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109002720 | ||||||
chr6:109003150
|
T | C | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-807A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003150 | ||||||
chr6:109003250
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-907G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003250 | ||||||
chr6:109003372
|
T | TGGGGTG | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1035_280-1030d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003372 | ||||||
chr6:109003499
|
G | T | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-1156C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003499 | ||||||
chr6:109003715
|
TA | T | 2 | a0001c0001t0008g0051a0001c0001t0008g0052 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-1373delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003715 | ||||||
chr6:109003782
|
G | GCCATTTA others(4): Show |
1 | a0002c0002t0002g0037 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.280-1450_280-1440d others(13): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003782 | ||||||
chr6:109004011
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-1668C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004011 | ||||||
chr6:109004014
|
T | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-1671A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004014 | ||||||
chr6:109004421
|
C | A | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-2078G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004421 | ||||||
chr6:109004422
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.280-2079C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004422 | ||||||
chr6:109004438
|
C | CT | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0179others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-2096dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004438 | ||||||
chr6:109004584
|
C | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-2241G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004584 | ||||||
chr6:109004608
|
TTTTAGTA others(2): Show |
T | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-2274_280-2266d others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004608 | ||||||
chr6:109004618
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-2275C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004618 | ||||||
chr6:109004622
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-2279C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004622 | ||||||
chr6:109004682
|
G | A | 17 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-2339C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004682 | ||||||
chr6:109004719
|
G | A | 8 | a0002c0002t0002g0035a0002c0002t0002g0037a0002c0002t0002g0038others(5): Show | 8 | HG00438.hp1 NA18951.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-2376C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004719 | ||||||
chr6:109004759
|
C | CACAG | 39 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.280-2420_280-2417d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004759 | ||||||
chr6:109004931
|
T | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0128others(1): Show | 4 | HG00323.hp2 HG02523.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2588A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004931 | ||||||
chr6:109004980
|
A | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.280-2637T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004980 | ||||||
chr6:109005418
|
T | G | 32 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-3075A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005418 | ||||||
chr6:109005537
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-3194T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005537 | ||||||
chr6:109005596
|
T | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-3253A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005596 | ||||||
chr6:109005632
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280-3289C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005632 | ||||||
chr6:109005685
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-3342C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005685 | ||||||
chr6:109005707
|
C | T | 2 | a0001c0001t0008g0051a0001c0001t0008g0052 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-3364G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005707 | ||||||
chr6:109005727
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.280-3384A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005727 | ||||||
chr6:109006084
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-3741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006084 | ||||||
chr6:109006205
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-3862T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006205 | ||||||
chr6:109006280
|
A | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-3937T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006280 | ||||||
chr6:109006336
|
A | C | 1 | a0001c0003t0004g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280-3993T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006336 | ||||||
chr6:109006379
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-4036T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006379 | ||||||
chr6:109006387
|
T | G | 1 | a0002c0002t0002g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.280-4044A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006387 | ||||||
chr6:109006449
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.280-4106T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006449 | ||||||
chr6:109006469
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.280-4126G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006469 | ||||||
chr6:109007040
|
T | C | 2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.280-4697A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007040 | ||||||
chr6:109007225
|
CTA | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.280-4884_280-4883d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007225 | ||||||
chr6:109007229
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-4886C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007229 | ||||||
chr6:109007309
|
T | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0094others(5): Show | 8 | HG02083.hp2 HG02129.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-4966A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007309 | ||||||
chr6:109007556
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.280-5213G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007556 | ||||||
chr6:109007570
|
G | A | 1 | a0001c0001t0003g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.280-5227C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007570 | ||||||
chr6:109007718
|
ACTAAC | A | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5380_280-5376d others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007718 | ||||||
chr6:109007723
|
C | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0171 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.280-5380G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007723 | ||||||
chr6:109007724
|
A | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5381T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007724 | ||||||
chr6:109007773
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-5430T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007773 | ||||||
chr6:109007785
|
CT | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0025others(17): Show | 20 | HG01257.hp2 HG02004.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.280-5443delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | ||||||
chr6:109007785
|
CTT | C | 29 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-5444_280-5443d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | ||||||
chr6:109007785
|
CTTTTTT | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-5448_280-5443d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | ||||||
chr6:109007857
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.280-5514C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007857 | ||||||
chr6:109008130
|
C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-5787G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008130 | ||||||
chr6:109008187
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280-5844C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008187 | ||||||
chr6:109008270
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-5927C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008270 | ||||||
chr6:109008334
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.280-5991A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008334 | ||||||
chr6:109008438
|
A | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-6095T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008438 | ||||||
chr6:109008450
|
AT | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6108delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008450 | ||||||
chr6:109008454
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-6111A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008454 | ||||||
chr6:109008792
|
C | T | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.280-6449G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008792 | ||||||
chr6:109008803
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-6460C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008803 | ||||||
chr6:109008916
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.280-6573C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008916 | ||||||
chr6:109008977
|
C | A | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280-6634G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008977 | ||||||
chr6:109009164
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6821T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009164 | ||||||
chr6:109009214
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6871G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009214 | ||||||
chr6:109009515
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-7172G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009515 | ||||||
chr6:109009532
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-7189T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009532 | ||||||
chr6:109009555
|
CG | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.280-7213delC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009555 | ||||||
chr6:109009656
|
C | T | 61 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.280-7313G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009656 | ||||||
chr6:109009725
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.280-7382T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009725 | ||||||
chr6:109010306
|
C | A | 18 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-7963G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010306 | ||||||
chr6:109010355
|
TTC | T | 2 | a0001c0001t0001g0130a0001c0001t0003g0131 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.280-8014_280-8013d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010355 | ||||||
chr6:109010574
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-8231T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010574 | ||||||
chr6:109010672
|
T | C | 9 | a0001c0001t0001g0072a0001c0001t0001g0136a0001c0001t0001g0143others(6): Show | 9 | HG02293.hp1 HG02818.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-8329A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010672 | ||||||
chr6:109011008
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-8665T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011008 | ||||||
chr6:109011136
|
C | G | 2 | a0001c0001t0006g0070a0001c0001t0006g0091 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.280-8793G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011136 | ||||||
chr6:109011467
|
T | C | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.280-9124A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011467 | ||||||
chr6:109011494
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280-9151T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011494 | ||||||
chr6:109011632
|
CT | C | 29 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-9290delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011632 | ||||||
chr6:109011660
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280-9317G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011660 | ||||||
chr6:109011792
|
C | A | 2 | a0001c0004t0005g0020a0001c0004t0005g0021 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-9449G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011792 | ||||||
chr6:109011843
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-9500C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011843 | ||||||
chr6:109011892
|
G | C | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.280-9549C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011892 | ||||||
chr6:109011904
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-9561G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011904 | ||||||
chr6:109011927
|
C | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9584G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011927 | ||||||
chr6:109012244
|
C | CT | 7 | a0001c0001t0001g0063a0001c0003t0004g0002a0001c0003t0004g0003others(4): Show | 7 | HG00639.hp2 HG02572.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-9902dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012244 | ||||||
chr6:109012623
|
A | T | 17 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-10280T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012623 | ||||||
chr6:109012881
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-10538C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012881 | ||||||
chr6:109012933
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-10590C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012933 | ||||||
chr6:109012959
|
C | CA | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-10617dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012959 | ||||||
chr6:109013097
|
AG | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-10755delC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013097 | ||||||
chr6:109013100
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-10757C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013100 | ||||||
chr6:109013255
|
C | G | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-10912G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013255 | ||||||
chr6:109013434
|
T | G | 13 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.280-11091A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013434 | ||||||
chr6:109013520
|
A | C | 1 | a0002c0002t0002g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280-11177T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013520 | ||||||
chr6:109013768
|
C | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-11425G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013768 | ||||||
chr6:109013906
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0105others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-11563A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013906 | ||||||
chr6:109014157
|
G | A | 3 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0044 | 3 | HG00280.hp2 HG01123.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.280-11814C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014157 | ||||||
chr6:109014239
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-11896T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014239 | ||||||
chr6:109014257
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-11914C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014257 | ||||||
chr6:109014431
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280-12088C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014431 | ||||||
chr6:109014743
|
T | C | 15 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0058others(12): Show | 15 | HG01257.hp2 HG02004.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-12400A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014743 | ||||||
chr6:109014766
|
C | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-12423G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014766 | ||||||
chr6:109014848
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-12505C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014848 | ||||||
chr6:109015414
|
A | G | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-13071T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109015414 | ||||||
chr6:109015777
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-13434G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109015777 | ||||||
chr6:109016368
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-14025A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016368 | ||||||
chr6:109016520
|
G | A | 30 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.280-14177C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016520 | ||||||
chr6:109016574
|
G | A | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.280-14231C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016574 | ||||||
chr6:109016907
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14564A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016907 | ||||||
chr6:109016944
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14601G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016944 | ||||||
chr6:109016958
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14615A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016958 | ||||||
chr6:109016984
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-14641G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016984 | ||||||
chr6:109017198
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-14855A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017198 | ||||||
chr6:109017230
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14887G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017230 | ||||||
chr6:109017580
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0003g0131 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.280-15237G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017580 | ||||||
chr6:109018280
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.280-15937T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018280 | ||||||
chr6:109018311
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.280-15968A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018311 | ||||||
chr6:109018314
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0071 | 2 | HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.280-15971G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018314 | ||||||
chr6:109018569
|
AG | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-16227delC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018569 | ||||||
chr6:109018732
|
CA | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0177 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.280-16390delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018732 | ||||||
chr6:109018925
|
C | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-16582G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018925 | ||||||
chr6:109019078
|
TTAAA | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-16739_280-1673 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019078 | ||||||
chr6:109019088
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-16745G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019088 | ||||||
chr6:109019343
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.280-17000T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019343 | ||||||
chr6:109019355
|
G | A | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-17012C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019355 | ||||||
chr6:109019495
|
A | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-17152T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019495 | ||||||
chr6:109019611
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-17268T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019611 | ||||||
chr6:109019670
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-17327T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019670 | ||||||
chr6:109019965
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-17622G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019965 | ||||||
chr6:109020095
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-17752T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020095 | ||||||
chr6:109020175
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.280-17832C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020175 | ||||||
chr6:109020192
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280-17849A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020192 | ||||||
chr6:109020589
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-18246T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020589 | ||||||
chr6:109020631
|
C | T | 65 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-18288G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020631 | ||||||
chr6:109020638
|
GAGA | G | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-18298_280-1829 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020638 | ||||||
chr6:109020796
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.280-18453G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020796 | ||||||
chr6:109020966
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-18623A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020966 | ||||||
chr6:109021330
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.280-18987A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021330 | ||||||
chr6:109021440
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.280-19097C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021440 | ||||||
chr6:109021456
|
T | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0123 | 2 | HG01168.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.280-19113A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021456 | ||||||
chr6:109021490
|
T | G | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-19147A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021490 | ||||||
chr6:109021554
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.280-19211G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021554 | ||||||
chr6:109021596
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-19253G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021596 | ||||||
chr6:109022049
|
A | ATT | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-19708_280-1970 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022049 | ||||||
chr6:109022137
|
A | T | 65 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-19794T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022137 | ||||||
chr6:109022353
|
C | T | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-20010G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022353 | ||||||
chr6:109022411
|
C | CT | 19 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0054others(16): Show | 19 | HG01109.hp2 HG01361.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-20069dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022411
|
CT | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0067others(21): Show | 24 | HG00323.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.280-20069delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022411
|
CTT | C | 37 | a0001c0001t0001g0019a0001c0001t0001g0060a0001c0001t0001g0063others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.280-20070_280-2006 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022411
|
CTTTTTT | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-20074_280-2006 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022411
|
CTTTTTTT others(1): Show |
C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-20076_280-2006 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022411
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-20078_280-2006 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | ||||||
chr6:109022445
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-20102A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022445 | ||||||
chr6:109022537
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-20194G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022537 | ||||||
chr6:109022549
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-20206G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022549 | ||||||
chr6:109022599
|
A | G | 1 | a0002c0002t0002g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.280-20256T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022599 | ||||||
chr6:109022642
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-20299G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022642 | ||||||
chr6:109023402
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-21059G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023402 | ||||||
chr6:109023436
|
A | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21093T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023436 | ||||||
chr6:109023458
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-21115A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023458 | ||||||
chr6:109023772
|
T | G | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-21429A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023772 | ||||||
chr6:109023838
|
AAAT | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-21498_280-2149 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023838 | ||||||
chr6:109023863
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21520G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023863 | ||||||
chr6:109024288
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21945C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024288 | ||||||
chr6:109024727
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-22384A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024727 | ||||||
chr6:109024889
|
T | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.280-22546A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024889 | ||||||
chr6:109024981
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-22638T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024981 | ||||||
chr6:109025303
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.280-22960G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025303 | ||||||
chr6:109025415
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-23072T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025415 | ||||||
chr6:109025747
|
A | G | 9 | a0001c0001t0001g0072a0001c0001t0001g0136a0001c0001t0001g0143others(6): Show | 9 | HG02293.hp1 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-23404T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025747 | ||||||
chr6:109025854
|
A | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-23511T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025854 | ||||||
chr6:109025951
|
C | CT | 31 | a0001c0001t0001g0049a0001c0001t0003g0166a0001c0001t0010g0010others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.280-23609dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025951 | ||||||
chr6:109025951
|
C | CTT | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-23610_280-2360 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025951 | ||||||
chr6:109026059
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-23716G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026059 | ||||||
chr6:109026119
|
A | G | 3 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-23776T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026119 | ||||||
chr6:109026528
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-24185G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026528 | ||||||
chr6:109026609
|
A | T | 2 | a0001c0003t0004g0005a0001c0003t0004g0006 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.280-24266T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026609 | ||||||
chr6:109026672
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-24329A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026672 | ||||||
chr6:109026690
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-24347G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026690 | ||||||
chr6:109026724
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-24381G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026724 | ||||||
chr6:109026756
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-24413C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026756 | ||||||
chr6:109026777
|
G | A | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-24434C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026777 | ||||||
chr6:109026798
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280-24455G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026798 | ||||||
chr6:109026943
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.280-24600T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026943 | ||||||
chr6:109027084
|
C | T | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-24741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027084 | ||||||
chr6:109027434
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0179a0001c0001t0008g0050others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-25091C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027434 | ||||||
chr6:109027476
|
C | CA | 10 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-25134dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | ||||||
chr6:109027476
|
C | CAAA | 6 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(3): Show | 6 | HG00280.hp2 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-25136_280-2513 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | ||||||
chr6:109027476
|
C | CAAAA | 21 | a0001c0001t0001g0147a0001c0003t0002g0182a0001c0003t0004g0005others(18): Show | 21 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.280-25137_280-2513 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | ||||||
chr6:109027476
|
C | CAAAAA | 6 | a0001c0001t0001g0049a0002c0002t0002g0014a0002c0002t0002g0026others(3): Show | 6 | HG00438.hp1 HG00639.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-25138_280-2513 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | ||||||
chr6:109027476
|
CA | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG00099.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-25134delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | ||||||
chr6:109028152
|
TC | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-25810delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028152 | ||||||
chr6:109028223
|
G | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0148 | 2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.280-25880C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028223 | ||||||
chr6:109028593
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.280-26250C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028593 | ||||||
chr6:109028690
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-26347C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028690 | ||||||
chr6:109028925
|
C | A | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-26582G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028925 | ||||||
chr6:109028979
|
T | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-26636A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028979 | ||||||
chr6:109029018
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-26675T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029018 | ||||||
chr6:109029087
|
C | T | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-26744G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029087 | ||||||
chr6:109029148
|
G | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-26805C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029148 | ||||||
chr6:109029178
|
T | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0086 | 2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.280-26835A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029178 | ||||||
chr6:109029286
|
G | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-26943C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029286 | ||||||
chr6:109029316
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-26973G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029316 | ||||||
chr6:109029347
|
T | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-27004A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029347 | ||||||
chr6:109029413
|
A | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-27070T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029413 | ||||||
chr6:109029590
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-27247C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029590 | ||||||
chr6:109029638
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.280-27295G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029638 | ||||||
chr6:109029656
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280-27313G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029656 | ||||||
chr6:109029922
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-27579T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029922 | ||||||
chr6:109030556
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.280-28213A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109030556 | ||||||
chr6:109031342
|
G | A | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-28999C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031342 | ||||||
chr6:109031401
|
C | A | 1 | a0002c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.280-29058G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031401 | ||||||
chr6:109031415
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG00280.hp1 HG02258.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.280-29072G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031415 | ||||||
chr6:109031498
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-29155G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031498 | ||||||
chr6:109031552
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-29209C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031552 | ||||||
chr6:109031596
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280-29253G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031596 | ||||||
chr6:109031702
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-29359A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031702 | ||||||
chr6:109032013
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-29670G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032013 | ||||||
chr6:109032204
|
G | A | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-29861C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032204 | ||||||
chr6:109032210
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-29867A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032210 | ||||||
chr6:109032212
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-29869G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032212 | ||||||
chr6:109032226
|
A | C | 65 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-29883T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032226 | ||||||
chr6:109032244
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-29901G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032244 | ||||||
chr6:109032316
|
C | A | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-29973G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032316 | ||||||
chr6:109032351
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-30008C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032351 | ||||||
chr6:109032378
|
G | C | 1 | a0002c0002t0002g0041 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-30035C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032378 | ||||||
chr6:109032617
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-30274G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032617 | ||||||
chr6:109032619
|
T | TG | 34 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(31): Show | 34 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.280-30277dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032619 | ||||||
chr6:109032659
|
T | C | 5 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-30316A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032659 | ||||||
chr6:109033657
|
G | T | 28 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-31314C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033657 | ||||||
chr6:109033706
|
T | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-31363A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033706 | ||||||
chr6:109033823
|
A | C | 1 | a0001c0001t0003g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.280-31480T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033823 | ||||||
chr6:109034158
|
T | C | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-31815A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034158 | ||||||
chr6:109034469
|
T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-32126A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034469 | ||||||
chr6:109034514
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-32171A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034514 | ||||||
chr6:109034587
|
G | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-32244C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034587 | ||||||
chr6:109034683
|
A | G | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-32340T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034683 | ||||||
chr6:109034808
|
C | G | 28 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-32465G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034808 | ||||||
chr6:109034901
|
A | T | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-32558T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034901 | ||||||
chr6:109035386
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-33043G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035386 | ||||||
chr6:109035548
|
G | GA | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-33206dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035548 | ||||||
chr6:109035794
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-33451C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035794 | ||||||
chr6:109035887
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-33544G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035887 | ||||||
chr6:109036121
|
G | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-33778C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036121 | ||||||
chr6:109036498
|
T | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-34155A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036498 | ||||||
chr6:109036626
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-34283T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036626 | ||||||
chr6:109036936
|
TA | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0123others(1): Show | 4 | HG01168.hp1 HG02486.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-34594delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036936 | ||||||
chr6:109037043
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.280-34700A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037043 | ||||||
chr6:109037142
|
C | G | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-34799G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037142 | ||||||
chr6:109037587
|
T | G | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.280-35244A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037587 | ||||||
chr6:109037911
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-35568A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037911 | ||||||
chr6:109037914
|
GCTGA | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-35575_280-3557 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037914 | ||||||
chr6:109038484
|
GC | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.280-36142delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038484 | ||||||
chr6:109038760
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-36417C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038760 | ||||||
chr6:109038911
|
A | AAGG | 29 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-36571_280-3656 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038911 | ||||||
chr6:109038911
|
A | AAGGAGG | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-36574_280-3656 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038911 | ||||||
chr6:109038985
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-36642T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038985 | ||||||
chr6:109039041
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36698T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039041 | ||||||
chr6:109039045
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36702T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039045 | ||||||
chr6:109039046
|
G | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36703C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039046 | ||||||
chr6:109039046
|
G | GGGA | 104 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.280-36706_280-3670 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039046 | ||||||
chr6:109039154
|
G | GAGGAGAA others(9): Show |
32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-36812_280-3681 others(20): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039154 | ||||||
chr6:109039407
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280-37064A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039407 | ||||||
chr6:109039502
|
C | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-37159G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039502 | ||||||
chr6:109039545
|
T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-37202A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039545 | ||||||
chr6:109039641
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-37298A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039641 | ||||||
chr6:109039742
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-37399G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039742 | ||||||
chr6:109040224
|
A | G | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-37881T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040224 | ||||||
chr6:109040292
|
C | T | 3 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-37949G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040292 | ||||||
chr6:109040329
|
CTG | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-37988_280-3798 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040329 | ||||||
chr6:109040519
|
G | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-38176C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040519 | ||||||
chr6:109040572
|
C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-38229G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040572 | ||||||
chr6:109040657
|
C | CT | 6 | a0001c0001t0010g0010a0001c0004t0005g0020a0001c0004t0005g0021others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-38315dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040657 | ||||||
chr6:109040657
|
C | CTT | 31 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.280-38316_280-3831 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040657 | ||||||
chr6:109040714
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38371C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040714 | ||||||
chr6:109040935
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-38592T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040935 | ||||||
chr6:109040962
|
T | A | 2 | a0001c0001t0006g0070a0001c0001t0006g0091 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.280-38619A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040962 | ||||||
chr6:109040999
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38656C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040999 | ||||||
chr6:109041042
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-38699G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041042 | ||||||
chr6:109041047
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.280-38704A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041047 | ||||||
chr6:109041133
|
T | C | 1 | a0002c0002t0002g0035 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.280-38790A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041133 | ||||||
chr6:109041138
|
T | TA | 5 | a0001c0001t0001g0126a0001c0004t0005g0020a0001c0004t0005g0021others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38796dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041138 | ||||||
chr6:109041138
|
TA | T | 33 | a0001c0001t0001g0049a0001c0001t0003g0176a0001c0001t0003g0178others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-38796delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041138 | ||||||
chr6:109041149
|
A | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-38806T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041149 | ||||||
chr6:109041324
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280-38981A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041324 | ||||||
chr6:109041524
|
AT | A | 28 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(25): Show | 28 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-39182delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041524 | ||||||
chr6:109041546
|
T | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-39203A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041546 | ||||||
chr6:109041921
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-39578A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041921 | ||||||
chr6:109042014
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-39671G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042014 | ||||||
chr6:109042171
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-39828T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042171 | ||||||
chr6:109042177
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-39834A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042177 | ||||||
chr6:109042312
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | NA19012.hp2 NA19063.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-39969A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042312 | ||||||
chr6:109042442
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280-40099T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042442 | ||||||
chr6:109042530
|
C | CA | 36 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0088others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.280-40188_280-4018 others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042530 | ||||||
chr6:109042531
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.280-40188C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042531 | ||||||
chr6:109042768
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0100 | 3 | HG00140.hp2 HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.280-40425T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042768 | ||||||
chr6:109042868
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-40525T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042868 | ||||||
chr6:109043463
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-41120T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043463 | ||||||
chr6:109043495
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-41152A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043495 | ||||||
chr6:109043622
|
G | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-41279C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043622 | ||||||
chr6:109044054
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-41711G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044054 | ||||||
chr6:109044064
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-41721G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044064 | ||||||
chr6:109044122
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-41779G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044122 | ||||||
chr6:109044191
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280-41848C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044191 | ||||||
chr6:109044213
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.280-41870C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044213 | ||||||
chr6:109044311
|
C | CA | 32 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0034others(29): Show | 33 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-41969dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
C | CAA | 15 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0024others(12): Show | 15 | HG01891.hp1 HG02004.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.280-41970_280-4196 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
C | CAAA | 7 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0071others(4): Show | 7 | HG02027.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-41971_280-4196 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CA | C | 14 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0077others(11): Show | 14 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.280-41969delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA | C | 7 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(4): Show | 7 | HG02027.hp2 HG02572.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-41975_280-4196 others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA others(1): Show |
C | 17 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0125others(14): Show | 17 | HG01109.hp1 HG01169.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.280-41976_280-4196 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0003g0135a0001c0001t0010g0010 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.280-41978_280-4196 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-41981_280-4196 others(17): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA others(11): Show |
C | 27 | a0001c0001t0001g0049a0001c0001t0001g0087a0001c0003t0002g0182others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-41986_280-4196 others(22): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044311
|
CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0002g0037 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.280-41987_280-4196 others(23): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | ||||||
chr6:109044430
|
C | T | 1 | a0001c0001t0011g0146 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.280-42087G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044430 | ||||||
chr6:109044556
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-42213T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044556 | ||||||
chr6:109044572
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-42229T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044572 | ||||||
chr6:109044708
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-42365G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044708 | ||||||
chr6:109044868
|
A | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-42525T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044868 | ||||||
chr6:109044884
|
G | A | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-42541C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044884 | ||||||
chr6:109044891
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-42548G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044891 | ||||||
chr6:109044980
|
G | A | 1 | a0001c0003t0004g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.280-42637C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044980 | ||||||
chr6:109045103
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.280-42760C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045103 | ||||||
chr6:109045212
|
A | G | 2 | a0001c0005t0001g0008a0001c0005t0001g0009 | 2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.280-42869T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045212 | ||||||
chr6:109045291
|
CT | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-42949delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045291 | ||||||
chr6:109045319
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-42976G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045319 | ||||||
chr6:109045423
|
C | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-43080G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045423 | ||||||
chr6:109045454
|
GCATATAA others(3): Show |
G | 33 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 33 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-43121_280-4311 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045454 | ||||||
chr6:109045480
|
C | G | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.280-43137G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045480 | ||||||
chr6:109045536
|
A | G | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-43193T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045536 | ||||||
chr6:109045537
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-43194C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045537 | ||||||
chr6:109045628
|
A | G | 18 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-43285T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045628 | ||||||
chr6:109045750
|
T | C | 15 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(12): Show | 15 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-43407A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045750 | ||||||
chr6:109045854
|
TAC | T | 3 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-43513_280-4351 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045854 | ||||||
chr6:109045860
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-43517C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045860 | ||||||
chr6:109045966
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-43623G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045966 | ||||||
chr6:109046027
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.280-43684A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046027 | ||||||
chr6:109046052
|
T | C | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-43709A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046052 | ||||||
chr6:109046084
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.280-43741T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046084 | ||||||
chr6:109046100
|
G | GCCCTCT | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-43763_280-4375 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046100 | ||||||
chr6:109046141
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-43798C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046141 | ||||||
chr6:109046157
|
T | G | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-43814A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046157 | ||||||
chr6:109046229
|
G | A | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-43886C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046229 | ||||||
chr6:109046229
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0109 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.280-43886C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046229 | ||||||
chr6:109046294
|
G | A | 16 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(13): Show | 16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-43951C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046294 | ||||||
chr6:109046343
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.280-44000G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046343 | ||||||
chr6:109046352
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-44009G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046352 | ||||||
chr6:109046416
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44073T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046416 | ||||||
chr6:109046451
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-44108G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046451 | ||||||
chr6:109046499
|
C | T | 1 | a0001c0001t0003g0170 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.280-44156G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046499 | ||||||
chr6:109046503
|
A | AC | 5 | a0001c0001t0001g0144a0001c0001t0003g0170a0001c0004t0005g0022others(2): Show | 5 | HG01169.hp2 HG02055.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44161dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046503 | ||||||
chr6:109046540
|
A | G | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44197T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046540 | ||||||
chr6:109046602
|
G | A | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-44259C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046602 | ||||||
chr6:109046615
|
C | T | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44272G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046615 | ||||||
chr6:109046628
|
A | G | 1 | a0002c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.280-44285T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046628 | ||||||
chr6:109046682
|
G | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44339C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046682 | ||||||
chr6:109046692
|
G | A | 1 | a0001c0001t0008g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-44349C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046692 | ||||||
chr6:109046720
|
C | T | 7 | a0001c0001t0003g0161a0001c0001t0003g0164a0001c0001t0003g0165others(4): Show | 7 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-44377G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046720 | ||||||
chr6:109046757
|
T | C | 34 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0010g0010others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.280-44414A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046757 | ||||||
chr6:109046772
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG02109.hp1 HG02293.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-44429C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046772 | ||||||
chr6:109046779
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.280-44436G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046779 | ||||||
chr6:109046800
|
C | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-44457G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046800 | ||||||
chr6:109046856
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-44513G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046856 | ||||||
chr6:109046859
|
A | C | 4 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0128others(1): Show | 4 | HG00323.hp2 HG02523.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-44516T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046859 | ||||||
chr6:109046882
|
T | C | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44539A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046882 | ||||||
chr6:109046897
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0097a0001c0001t0001g0114others(2): Show | 5 | HG02083.hp2 NA18747.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-44554C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046897 | ||||||
chr6:109046925
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44582C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046925 | ||||||
chr6:109046928
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44585T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046928 | ||||||
chr6:109046955
|
G | A | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44612C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046955 | ||||||
chr6:109046961
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44618T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046961 | ||||||
chr6:109046965
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-44622C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046965 | ||||||
chr6:109046986
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44643C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046986 | ||||||
chr6:109047006
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-44663G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047006 | ||||||
chr6:109047009
|
T | C | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44666A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047009 | ||||||
chr6:109047027
|
A | ATCCGGGA others(92): Show |
1 | a0002c0002t0002g0029 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.280-44685_280-4468 others(103): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | ||||||
chr6:109047027
|
A | ATCCGGGA others(91): Show |
5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | ||||||
chr6:109047027
|
A | ATCCGGGA others(91): Show |
25 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | ||||||
chr6:109047027
|
A | ATCCGGGA others(91): Show |
1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | ||||||
chr6:109047041
|
T | TGGGGGGG others(671): Show |
1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
1 | a0001c0001t0003g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(673): Show |
1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(684): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0003g0161 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
11 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0067others(8): Show | 11 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
2 | a0001c0001t0001g0060a0001c0001t0001g0094 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
2 | a0001c0001t0003g0160a0001c0001t0003g0162 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(493): Show |
4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(504): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(493): Show |
1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(504): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(495): Show |
1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(506): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0003g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
15 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(12): Show | 15 | HG02027.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(1071): Show |
2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG01109.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(1082): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
4 | a0001c0001t0001g0122a0001c0001t0006g0070a0001c0001t0006g0091others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(670): Show |
86 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047041
|
T | TGGGGGGT others(671): Show |
1 | a0001c0005t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | ||||||
chr6:109047042
|
G | GGGGGGTC others(671): Show |
2 | a0001c0004t0005g0020a0001c0004t0005g0021 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-44700_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047042 | ||||||
chr6:109047042
|
G | GGGGGGTC others(670): Show |
3 | a0001c0001t0013g0015a0001c0004t0005g0022a0001c0004t0005g0023 | 3 | HG01168.hp2 HG01169.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.280-44700_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047042 | ||||||
chr6:109047055
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44712A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047055 | ||||||
chr6:109047058
|
A | G | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44715T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047058 | ||||||
chr6:109047075
|
A | G | 28 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-44732T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047075 | ||||||
chr6:109047078
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44735A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047078 | ||||||
chr6:109047135
|
T | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44792A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047135 | ||||||
chr6:109047139
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0001g0100a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44796G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047139 | ||||||
chr6:109047148
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44805C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047148 | ||||||
chr6:109047152
|
G | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44809C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047152 | ||||||
chr6:109047157
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44814C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047157 | ||||||
chr6:109047166
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44823C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047166 | ||||||
chr6:109047178
|
G | GC | 28 | a0001c0001t0001g0049a0001c0001t0003g0176a0001c0003t0002g0182others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-44836dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047178 | ||||||
chr6:109047184
|
C | CCACCCGG others(347): Show |
5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44842_280-4484 others(358): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047184 | ||||||
chr6:109047185
|
G | A | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44842C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047185 | ||||||
chr6:109047189
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44846C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047189 | ||||||
chr6:109047201
|
C | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44858G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047201 | ||||||
chr6:109047231
|
T | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44888A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047231 | ||||||
chr6:109047237
|
C | T | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44894G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047237 | ||||||
chr6:109047247
|
C | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44904G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047247 | ||||||
chr6:109047251
|
G | A | 26 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-44908C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047251 | ||||||
chr6:109047254
|
T | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44911A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047254 | ||||||
chr6:109047311
|
T | A | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44968A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047311 | ||||||
chr6:109047312
|
G | GCCTGGCC others(269): Show |
1 | a0002c0002t0002g0029 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.280-44970_280-4496 others(280): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | ||||||
chr6:109047312
|
G | GCCTGGCC others(268): Show |
25 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.280-44970_280-4496 others(279): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | ||||||
chr6:109047312
|
G | GCCTGGCC others(268): Show |
1 | a0002c0002t0002g0031 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.280-44970_280-4496 others(279): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | ||||||
chr6:109047316
|
G | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-44973C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047316 | ||||||
chr6:109047323
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44980G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047323 | ||||||
chr6:109047358
|
C | T | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45015G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047358 | ||||||
chr6:109047360
|
T | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45017A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047360 | ||||||
chr6:109047364
|
C | T | 16 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(13): Show | 16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-45021G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047364 | ||||||
chr6:109047373
|
G | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-45030C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047373 | ||||||
chr6:109047381
|
C | T | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45038G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047381 | ||||||
chr6:109047405
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-45062G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047405 | ||||||
chr6:109047456
|
A | G | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45113T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047456 | ||||||
chr6:109047499
|
C | T | 28 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-45156G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047499 | ||||||
chr6:109047505
|
G | A | 1 | a0003c0006t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280-45162C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047505 | ||||||
chr6:109047532
|
C | T | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280-45189G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047532 | ||||||
chr6:109047650
|
A | G | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.280-45307T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047650 | ||||||
chr6:109047655
|
G | C | 34 | a0001c0001t0001g0049a0001c0001t0001g0118a0001c0001t0010g0010others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.280-45312C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047655 | ||||||
chr6:109047696
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280-45353C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047696 | ||||||
chr6:109047745
|
C | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-45402G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047745 | ||||||
chr6:109047856
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-45513A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047856 | ||||||
chr6:109047903
|
G | C | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45560C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047903 | ||||||
chr6:109047904
|
G | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-45561C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047904 | ||||||
chr6:109047910
|
A | AGTCATCA others(7): Show |
2 | a0001c0004t0005g0020a0001c0004t0005g0021 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-45581_280-4556 others(18): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047910 | ||||||
chr6:109047921
|
C | A | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45578G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047921 | ||||||
chr6:109047938
|
C | A | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45595G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047938 | ||||||
chr6:109047939
|
C | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45596G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047939 | ||||||
chr6:109047952
|
C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-45609G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047952 | ||||||
chr6:109047966
|
A | G | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45623T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047966 | ||||||
chr6:109048043
|
A | G | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-45700T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048043 | ||||||
chr6:109048104
|
TA | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.279+45690delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048104 | ||||||
chr6:109048104
|
TAA | T | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0001t0013g0015others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+45689_279+4569 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048104 | ||||||
chr6:109048106
|
A | T | 16 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(13): Show | 16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.279+45689T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048106 | ||||||
chr6:109048200
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+45595A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048200 | ||||||
chr6:109048367
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+45428T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048367 | ||||||
chr6:109048542
|
T | C | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+45253A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048542 | ||||||
chr6:109048624
|
G | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+45171C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048624 | ||||||
chr6:109048637
|
C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+45158G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048637 | ||||||
chr6:109048646
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+45149C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048646 | ||||||
chr6:109048800
|
T | C | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+44995A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048800 | ||||||
chr6:109048803
|
A | G | 53 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(50): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+44992T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048803 | ||||||
chr6:109048824
|
T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+44971A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048824 | ||||||
chr6:109049008
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.279+44787G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049008 | ||||||
chr6:109049238
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+44557A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049238 | ||||||
chr6:109049287
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.279+44508G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049287 | ||||||
chr6:109049486
|
T | C | 22 | a0001c0001t0001g0053a0001c0001t0001g0097a0001c0001t0003g0135others(19): Show | 22 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+44309A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049486 | ||||||
chr6:109049620
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.279+44175G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049620 | ||||||
chr6:109049650
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.279+44145T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049650 | ||||||
chr6:109049694
|
G | A | 2 | a0001c0001t0003g0167a0001c0001t0003g0171 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.279+44101C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049694 | ||||||
chr6:109049926
|
T | C | 39 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.279+43869A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049926 | ||||||
chr6:109050371
|
G | A | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+43424C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050371 | ||||||
chr6:109050388
|
T | TA | 38 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.279+43406dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | ||||||
chr6:109050388
|
T | TAA | 14 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(11): Show | 14 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+43405_279+4340 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | ||||||
chr6:109050388
|
TA | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0117others(3): Show | 6 | HG01168.hp1 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+43406delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | ||||||
chr6:109050460
|
T | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+43335A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050460 | ||||||
chr6:109050506
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+43289C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050506 | ||||||
chr6:109050703
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.279+43092T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050703 | ||||||
chr6:109050765
|
ATCATAAG others(13): Show |
A | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279+43010_279+4302 others(24): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050765 | ||||||
chr6:109050863
|
C | A | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.279+42932G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050863 | ||||||
chr6:109050917
|
G | A | 32 | a0001c0001t0001g0049a0001c0003t0002g0182a0001c0003t0004g0002others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+42878C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050917 | ||||||
chr6:109051150
|
C | CA | 8 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+42644dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051150 | ||||||
chr6:109051163
|
C | CA | 26 | a0001c0001t0001g0049a0001c0001t0012g0163a0001c0003t0002g0182others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.279+42631dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051163 | ||||||
chr6:109051172
|
A | C | 3 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.279+42623T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051172 | ||||||
chr6:109051322
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+42473T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051322 | ||||||
chr6:109051325
|
GAGTC | G | 27 | a0001c0001t0001g0049a0001c0003t0002g0182a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+42466_279+4246 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051325 | ||||||
chr6:109051348
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+42447A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051348 | ||||||
chr6:109051557
|
C | T | 5 | a0001c0001t0001g0049a0002c0002t0002g0027a0002c0002t0002g0032others(2): Show | 5 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+42238G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051557 | ||||||
chr6:109051559
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+42236G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051559 | ||||||
chr6:109052306
|
T | TA | 5 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0126others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+41488dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052306 | ||||||
chr6:109052542
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.279+41253A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052542 | ||||||
chr6:109052798
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.279+40997T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052798 | ||||||
chr6:109053022
|
T | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.279+40773A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053022 | ||||||
chr6:109053045
|
G | GATGT | 3 | a0001c0001t0001g0179a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG03453.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.279+40746_279+4074 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053045 | ||||||
chr6:109053046
|
A | ATG | 5 | a0001c0001t0001g0100a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+40747_279+4074 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053046 | ||||||
chr6:109053046
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+40749T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053046 | ||||||
chr6:109053262
|
T | C | 33 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+40533A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053262 | ||||||
chr6:109053353
|
G | A | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+40442C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053353 | ||||||
chr6:109053502
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG03453.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.279+40293C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053502 | ||||||
chr6:109053778
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.279+40017C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053778 | ||||||
chr6:109054078
|
A | AT | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39716dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054078 | ||||||
chr6:109054084
|
T | G | 18 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+39711A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054084 | ||||||
chr6:109054154
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+39641C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054154 | ||||||
chr6:109054157
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+39638A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054157 | ||||||
chr6:109054252
|
G | A | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39543C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054252 | ||||||
chr6:109054370
|
A | G | 1 | a0001c0001t0003g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.279+39425T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054370 | ||||||
chr6:109054387
|
T | C | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39408A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054387 | ||||||
chr6:109054392
|
T | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+39403A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054392 | ||||||
chr6:109054736
|
T | C | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.279+39059A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054736 | ||||||
chr6:109054769
|
A | AC | 66 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.279+39025dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054769 | ||||||
chr6:109054915
|
T | C | 33 | a0001c0001t0001g0049a0001c0001t0010g0010a0001c0003t0002g0182others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+38880A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054915 | ||||||
chr6:109055117
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.279+38678A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055117 | ||||||
chr6:109055218
|
G | A | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279+38577C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055218 | ||||||
chr6:109055234
|
G | C | 1 | a0002c0002t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.279+38561C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055234 | ||||||
chr6:109055269
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+38526G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055269 | ||||||
chr6:109055421
|
G | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0074others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+38374C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055421 | ||||||
chr6:109055444
|
C | G | 26 | a0001c0001t0001g0049a0002c0002t0002g0013a0002c0002t0002g0014others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.279+38351G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055444 | ||||||
chr6:109055503
|
A | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+38292T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055503 | ||||||
chr6:109055505
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0009g0007 | 3 | HG02109.hp2 HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.279+38290T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055505 | ||||||
chr6:109055519
|
C | T | 23 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(20): Show | 23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+38276G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055519 | ||||||
chr6:109055520
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+38275C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055520 | ||||||
chr6:109055661
|
C | CA | 31 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(28): Show | 31 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+38133dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055661 | ||||||
chr6:109055661
|
CA | C | 6 | a0001c0001t0003g0135a0001c0001t0006g0070a0001c0001t0006g0091others(3): Show | 6 | HG02647.hp2 HG02735.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+38133delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055661 | ||||||
chr6:109055830
|
C | A | 66 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0053others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.279+37965G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055830 | ||||||
chr6:109055838
|
G | A | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+37957C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055838 | ||||||
chr6:109056185
|
T | C | 1 | a0001c0001t0006g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.279+37610A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056185 | ||||||
chr6:109056262
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+37533G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056262 | ||||||
chr6:109056408
|
AAAC | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+37384_279+3738 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056408 | ||||||
chr6:109056566
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+37229G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056566 | ||||||
chr6:109056667
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+37128G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056667 | ||||||
chr6:109056671
|
T | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+37124A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056671 | ||||||
chr6:109056848
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0123 | 3 | HG01168.hp1 HG02486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.279+36947C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056848 | ||||||
chr6:109057049
|
C | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+36746G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057049 | ||||||
chr6:109057169
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279+36626C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057169 | ||||||
chr6:109057285
|
A | T | 1 | a0001c0004t0005g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.279+36510T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057285 | ||||||
chr6:109057315
|
G | C | 6 | a0001c0003t0002g0182a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+36480C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057315 | ||||||
chr6:109057406
|
G | A | 27 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+36389C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057406 | ||||||
chr6:109057639
|
T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+36156A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057639 | ||||||
chr6:109057766
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.279+36029G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057766 | ||||||
chr6:109057867
|
G | A | 2 | a0001c0001t0006g0070a0001c0001t0006g0091 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.279+35928C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057867 | ||||||
chr6:109058037
|
C | CT | 15 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(12): Show | 15 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+35757dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058037 | ||||||
chr6:109058147
|
C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+35648G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058147 | ||||||
chr6:109058154
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+35641C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058154 | ||||||
chr6:109058579
|
CTAGATGC others(3): Show |
C | 5 | a0001c0001t0013g0015a0001c0004t0005g0020a0001c0004t0005g0021others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+35206_279+3521 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058579 | ||||||
chr6:109058623
|
A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+35172T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058623 | ||||||
chr6:109058667
|
ACCT | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+35125_279+3512 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058667 | ||||||
chr6:109058705
|
G | C | 14 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(11): Show | 14 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.279+35090C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058705 | ||||||
chr6:109058752
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0148 | 2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.279+35043T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058752 | ||||||
chr6:109058810
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.279+34985G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058810 | ||||||
chr6:109059096
|
T | TAC | 6 | a0001c0001t0001g0145a0001c0001t0001g0177a0001c0001t0008g0051others(3): Show | 6 | HG03453.hp2 HG03654.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+34697_279+3469 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059096 | ||||||
chr6:109059096
|
T | TACACACA others(11): Show |
4 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(1): Show | 4 | HG03225.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+34681_279+3469 others(22): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059096 | ||||||
chr6:109059118
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0008g0050 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+34677A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059118 | ||||||
chr6:109059431
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+34364C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059431 | ||||||
chr6:109059710
|
A | T | 7 | a0001c0001t0001g0126a0001c0001t0008g0050a0001c0003t0004g0002others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+34085T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059710 | ||||||
chr6:109059937
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+33858T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059937 | ||||||
chr6:109060210
|
G | T | 2 | a0001c0005t0001g0008a0001c0005t0001g0009 | 2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.279+33585C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060210 | ||||||
chr6:109060449
|
G | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.279+33346C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060449 | ||||||
chr6:109060897
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+32898G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060897 | ||||||
chr6:109061170
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+32625A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061170 | ||||||
chr6:109061423
|
A | G | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+32372T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061423 | ||||||
chr6:109061492
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+32303G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061492 | ||||||
chr6:109062071
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31724A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062071 | ||||||
chr6:109062197
|
C | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.279+31598G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062197 | ||||||
chr6:109062364
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.279+31431G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062364 | ||||||
chr6:109062373
|
C | T | 20 | a0001c0001t0001g0072a0001c0001t0001g0136a0001c0001t0001g0137others(17): Show | 20 | HG00438.hp2 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.279+31422G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062373 | ||||||
chr6:109062424
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0003t0004g0002others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+31371A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062424 | ||||||
chr6:109062456
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0049others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.279+31339A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062456 | ||||||
chr6:109062556
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31239C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062556 | ||||||
chr6:109062620
|
C | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31175G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062620 | ||||||
chr6:109062924
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279+30871T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062924 | ||||||
chr6:109063073
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+30722A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063073 | ||||||
chr6:109063109
|
C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+30686G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063109 | ||||||
chr6:109063275
|
G | GA | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+30519dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063275 | ||||||
chr6:109063362
|
C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+30433G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063362 | ||||||
chr6:109063433
|
A | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+30362T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063433 | ||||||
chr6:109063511
|
T | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+30284A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063511 | ||||||
chr6:109063615
|
G | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+30180C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063615 | ||||||
chr6:109063731
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+30064A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063731 | ||||||
chr6:109063758
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+30037C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063758 | ||||||
chr6:109063892
|
T | TA | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29902dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063892 | ||||||
chr6:109064076
|
T | C | 19 | a0001c0001t0001g0126a0001c0001t0003g0135a0001c0001t0003g0159others(16): Show | 19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+29719A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064076 | ||||||
chr6:109064443
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+29352A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064443 | ||||||
chr6:109064448
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29347T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064448 | ||||||
chr6:109064576
|
A | G | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+29219T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064576 | ||||||
chr6:109064584
|
A | AGAGAGAG others(9): Show |
1 | a0001c0001t0001g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.279+29210_279+2921 others(20): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | ||||||
chr6:109064584
|
A | AGAGGAGA others(28): Show |
1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+29210_279+2921 others(39): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | ||||||
chr6:109064584
|
A | AGAGGGGA others(8): Show |
1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+29210_279+2921 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | ||||||
chr6:109064589
|
A | AGAGGG | 52 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0053others(49): Show | 52 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+29201_279+2920 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | AGAGGGGA others(3): Show |
22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(19): Show | 22 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+29196_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | AGAGGGGA others(8): Show |
13 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+29191_279+2920 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | AGAGGGGA others(13): Show |
1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.279+29186_279+2920 others(24): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | AGAGGGGA others(18): Show |
1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.279+29181_279+2920 others(29): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | AGAGGGGA others(23): Show |
3 | a0002c0002t0002g0027a0002c0002t0002g0032a0002c0002t0002g0033 | 3 | HG00280.hp2 HG01175.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.279+29176_279+2920 others(34): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0179a0001c0001t0006g0091others(1): Show | 4 | HG00738.hp2 HG02647.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+29206T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
AGAGGG | A | 4 | a0001c0001t0001g0148a0001c0001t0003g0135a0001c0001t0003g0176others(1): Show | 4 | HG01175.hp2 HG02258.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+29201_279+2920 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064589
|
AGAGGGGA others(3): Show |
A | 2 | a0001c0001t0001g0119a0001c0001t0001g0150 | 2 | HG02523.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.279+29196_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | ||||||
chr6:109064590
|
G | GAGGGGAG others(3): Show |
15 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(12): Show | 15 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+29204_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064590 | ||||||
chr6:109064605
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+29190C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064605 | ||||||
chr6:109064622
|
G | GGGGAGGG others(17): Show |
1 | a0002c0002t0002g0044 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.279+29172_279+2917 others(28): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064622 | ||||||
chr6:109064623
|
GGGAGGGG others(8): Show |
G | 1 | a0002c0002t0002g0048 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.279+29157_279+2917 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064623 | ||||||
chr6:109064629
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+29166C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064629 | ||||||
chr6:109064633
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29162C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064633 | ||||||
chr6:109064638
|
A | G | 32 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+29157T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064638 | ||||||
chr6:109064782
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29013G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064782 | ||||||
chr6:109064903
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+28892C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064903 | ||||||
chr6:109064954
|
G | A | 28 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(25): Show | 28 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.279+28841C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064954 | ||||||
chr6:109065009
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.279+28786G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065009 | ||||||
chr6:109065106
|
G | A | 27 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+28689C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065106 | ||||||
chr6:109065256
|
TA | T | 30 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+28538delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065256 | ||||||
chr6:109065628
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+28167T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065628 | ||||||
chr6:109065798
|
A | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+27997T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065798 | ||||||
chr6:109065809
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+27986T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065809 | ||||||
chr6:109065818
|
A | T | 7 | a0002c0002t0002g0028a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+27977T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065818 | ||||||
chr6:109065989
|
A | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+27806T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065989 | ||||||
chr6:109066312
|
CT | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0049a0001c0001t0001g0117others(13): Show | 16 | HG01168.hp1 HG01168.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.279+27482delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066312 | ||||||
chr6:109066414
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+27381C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066414 | ||||||
chr6:109066508
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+27287G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066508 | ||||||
chr6:109066883
|
G | GTAAGTCA others(3): Show |
67 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+26911_279+2691 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066883 | ||||||
chr6:109067034
|
G | C | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+26761C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067034 | ||||||
chr6:109067155
|
C | T | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+26640G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067155 | ||||||
chr6:109067212
|
C | T | 52 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+26583G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067212 | ||||||
chr6:109067396
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+26399A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067396 | ||||||
chr6:109067410
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+26385C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067410 | ||||||
chr6:109067740
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+26055A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067740 | ||||||
chr6:109067919
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.279+25876T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067919 | ||||||
chr6:109068006
|
T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+25789A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068006 | ||||||
chr6:109068048
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25747T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068048 | ||||||
chr6:109068062
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25733G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068062 | ||||||
chr6:109068196
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+25599A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068196 | ||||||
chr6:109068305
|
A | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+25490T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068305 | ||||||
chr6:109068333
|
G | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+25462C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068333 | ||||||
chr6:109068418
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25377T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068418 | ||||||
chr6:109068477
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25318C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068477 | ||||||
chr6:109068486
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.279+25309T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068486 | ||||||
chr6:109068611
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25184A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068611 | ||||||
chr6:109068721
|
C | CT | 18 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0079others(15): Show | 18 | HG00280.hp1 HG01099.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.279+25073dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068721 | ||||||
chr6:109068772
|
G | A | 5 | a0001c0001t0013g0015a0001c0004t0005g0020a0001c0004t0005g0021others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25023C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068772 | ||||||
chr6:109068807
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.279+24988C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068807 | ||||||
chr6:109068870
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+24925T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068870 | ||||||
chr6:109068880
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+24915G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068880 | ||||||
chr6:109069021
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+24774G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069021 | ||||||
chr6:109069116
|
T | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+24679A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069116 | ||||||
chr6:109069173
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.279+24622C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069173 | ||||||
chr6:109069206
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+24589C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069206 | ||||||
chr6:109069304
|
T | C | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+24491A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069304 | ||||||
chr6:109069331
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+24464T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069331 | ||||||
chr6:109069485
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.279+24310C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069485 | ||||||
chr6:109069567
|
G | C | 24 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+24228C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069567 | ||||||
chr6:109069700
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+24095G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069700 | ||||||
chr6:109069707
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+24088T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069707 | ||||||
chr6:109069743
|
A | AG | 30 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0093others(27): Show | 30 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+24051dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069743 | ||||||
chr6:109069745
|
G | C | 1 | a0001c0001t0014g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.279+24050C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069745 | ||||||
chr6:109069871
|
A | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+23924T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069871 | ||||||
chr6:109070095
|
T | C | 1 | a0003c0006t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.279+23700A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070095 | ||||||
chr6:109070111
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+23684T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070111 | ||||||
chr6:109070291
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+23504T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070291 | ||||||
chr6:109070321
|
T | G | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+23474A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070321 | ||||||
chr6:109070538
|
C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+23257G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070538 | ||||||
chr6:109070882
|
T | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22913A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070882 | ||||||
chr6:109071238
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22557G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071238 | ||||||
chr6:109071239
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279+22556C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071239 | ||||||
chr6:109071265
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22530T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071265 | ||||||
chr6:109071353
|
C | CTTTTTTT others(1): Show |
5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22434_279+2244 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071353 | ||||||
chr6:109071397
|
T | C | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+22398A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071397 | ||||||
chr6:109071434
|
T | G | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.279+22361A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071434 | ||||||
chr6:109071518
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.279+22277C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071518 | ||||||
chr6:109071788
|
C | T | 18 | a0001c0001t0003g0135a0001c0001t0003g0159a0001c0001t0003g0160others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+22007G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071788 | ||||||
chr6:109071955
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.279+21840A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071955 | ||||||
chr6:109072077
|
ATC | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21716_279+2171 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072077 | ||||||
chr6:109072195
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+21600A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072195 | ||||||
chr6:109072351
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21444A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072351 | ||||||
chr6:109072452
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+21343G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072452 | ||||||
chr6:109072672
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21123A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072672 | ||||||
chr6:109072899
|
AT | A | 6 | a0001c0001t0001g0087a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG02683.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+20895delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072899 | ||||||
chr6:109072964
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+20831C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072964 | ||||||
chr6:109073011
|
TTTTG | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0003t0002g0182others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+20780_279+2078 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073011 | ||||||
chr6:109073065
|
A | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+20730T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073065 | ||||||
chr6:109073093
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+20702C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073093 | ||||||
chr6:109073130
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.279+20665T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073130 | ||||||
chr6:109073244
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+20551G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073244 | ||||||
chr6:109073275
|
C | T | 4 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0005others(1): Show | 4 | HG02572.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+20520G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073275 | ||||||
chr6:109073322
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+20473G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073322 | ||||||
chr6:109073729
|
A | G | 3 | a0001c0001t0006g0070a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.279+20066T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073729 | ||||||
chr6:109073819
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.279+19976A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073819 | ||||||
chr6:109073868
|
C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+19927G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073868 | ||||||
chr6:109074306
|
A | ACC | 67 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+19487_279+1948 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074306 | ||||||
chr6:109074559
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+19236A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074559 | ||||||
chr6:109074607
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+19188T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074607 | ||||||
chr6:109074699
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.279+19096A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074699 | ||||||
chr6:109074744
|
C | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+19051G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074744 | ||||||
chr6:109074858
|
T | C | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+18937A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074858 | ||||||
chr6:109074981
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+18814T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074981 | ||||||
chr6:109075000
|
A | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+18795T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075000 | ||||||
chr6:109075125
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+18670G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075125 | ||||||
chr6:109075140
|
G | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(21): Show | 24 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+18655C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075140 | ||||||
chr6:109075723
|
C | T | 57 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.279+18072G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075723 | ||||||
chr6:109075806
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+17989A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075806 | ||||||
chr6:109075868
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+17927C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075868 | ||||||
chr6:109076046
|
C | T | 1 | a0001c0001t0016g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.279+17749G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076046 | ||||||
chr6:109076222
|
T | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+17573A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076222 | ||||||
chr6:109076224
|
T | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+17571A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076224 | ||||||
chr6:109076418
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02630.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+17377C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076418 | ||||||
chr6:109076662
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+17133G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076662 | ||||||
chr6:109076747
|
A | G | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+17048T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076747 | ||||||
chr6:109077054
|
C | T | 27 | a0001c0001t0001g0034a0001c0001t0001g0049a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+16741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077054 | ||||||
chr6:109077059
|
C | T | 1 | a0001c0003t0004g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+16736G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077059 | ||||||
chr6:109077215
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+16580T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077215 | ||||||
chr6:109077276
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0074others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+16519C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077276 | ||||||
chr6:109077291
|
C | A | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+16504G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077291 | ||||||
chr6:109077302
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+16493A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077302 | ||||||
chr6:109077533
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+16262G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077533 | ||||||
chr6:109077552
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+16243A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077552 | ||||||
chr6:109077651
|
A | G | 1 | a0001c0001t0016g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.279+16144T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077651 | ||||||
chr6:109078001
|
T | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+15794A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078001 | ||||||
chr6:109078170
|
C | T | 67 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+15625G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078170 | ||||||
chr6:109078194
|
A | C | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+15601T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078194 | ||||||
chr6:109078416
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.279+15379G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078416 | ||||||
chr6:109078436
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+15359G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078436 | ||||||
chr6:109078860
|
C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+14935G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078860 | ||||||
chr6:109078868
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+14927A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078868 | ||||||
chr6:109078951
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+14844C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078951 | ||||||
chr6:109079062
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+14733C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079062 | ||||||
chr6:109079076
|
T | C | 57 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.279+14719A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079076 | ||||||
chr6:109079194
|
G | GA | 145 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.279+14600dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079194 | ||||||
chr6:109079194
|
G | GAA | 25 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(22): Show | 25 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+14599_279+1460 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079194 | ||||||
chr6:109079355
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+14440T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079355 | ||||||
chr6:109079832
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.279+13963G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079832 | ||||||
chr6:109079842
|
G | T | 27 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+13953C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079842 | ||||||
chr6:109080170
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+13625G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080170 | ||||||
chr6:109080593
|
T | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.279+13202A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080593 | ||||||
chr6:109080652
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+13143T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080652 | ||||||
chr6:109080659
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+13136A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080659 | ||||||
chr6:109080914
|
C | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12881G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080914 | ||||||
chr6:109080998
|
T | G | 2 | a0002c0002t0002g0047a0002c0002t0002g0048 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.279+12797A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080998 | ||||||
chr6:109081041
|
C | CA | 28 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0003g0135others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+12753dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081041 | ||||||
chr6:109081075
|
C | G | 67 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+12720G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081075 | ||||||
chr6:109081207
|
A | G | 1 | a0001c0003t0004g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.279+12588T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081207 | ||||||
chr6:109081231
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12564A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081231 | ||||||
chr6:109081343
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.279+12452C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081343 | ||||||
chr6:109081368
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12427C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081368 | ||||||
chr6:109081437
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+12358G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081437 | ||||||
chr6:109081715
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12080A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081715 | ||||||
chr6:109081842
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.279+11953A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081842 | ||||||
chr6:109082122
|
T | C | 52 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+11673A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082122 | ||||||
chr6:109082216
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+11579T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082216 | ||||||
chr6:109082777
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.279+11018A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082777 | ||||||
chr6:109082963
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+10832C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082963 | ||||||
chr6:109083018
|
GTAT | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+10774_279+1077 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083018 | ||||||
chr6:109083463
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+10332T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083463 | ||||||
chr6:109083629
|
G | T | 1 | a0001c0001t0009g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+10166C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083629 | ||||||
chr6:109083952
|
C | T | 3 | a0001c0001t0008g0050a0001c0001t0008g0051a0001c0001t0008g0052 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.279+9843G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083952 | ||||||
chr6:109084058
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+9737G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084058 | ||||||
chr6:109084070
|
T | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.279+9725A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084070 | ||||||
chr6:109084122
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9673G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084122 | ||||||
chr6:109084199
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9596C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084199 | ||||||
chr6:109084407
|
A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+9388T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084407 | ||||||
chr6:109084423
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9372C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084423 | ||||||
chr6:109084425
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.279+9370C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084425 | ||||||
chr6:109084480
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9315C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084480 | ||||||
chr6:109084856
|
A | G | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(10): Show | 13 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+8939T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084856 | ||||||
chr6:109084998
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+8797G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084998 | ||||||
chr6:109085020
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+8775C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085020 | ||||||
chr6:109085041
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.279+8754A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085041 | ||||||
chr6:109085050
|
G | GT | 51 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.279+8744dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085050 | ||||||
chr6:109085096
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+8699A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085096 | ||||||
chr6:109085128
|
GA | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+8666delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085128 | ||||||
chr6:109085251
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.279+8544C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085251 | ||||||
chr6:109085310
|
T | G | 63 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.279+8485A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085310 | ||||||
chr6:109085347
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+8448C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085347 | ||||||
chr6:109085432
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+8363A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085432 | ||||||
chr6:109085445
|
G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+8350C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085445 | ||||||
chr6:109085500
|
C | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+8295G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085500 | ||||||
chr6:109085515
|
T | TCA | 8 | a0001c0001t0001g0123a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG00280.hp1 HG01106.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+8278_279+8279d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | ||||||
chr6:109085515
|
T | TCACACAC others(3): Show |
2 | a0001c0003t0004g0003a0001c0003t0004g0006 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.279+8270_279+8279d others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | ||||||
chr6:109085515
|
T | TCACACAC others(5): Show |
3 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005 | 3 | HG02572.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.279+8268_279+8279d others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | ||||||
chr6:109085515
|
TCA | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.279+8278_279+8279d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | ||||||
chr6:109085515
|
TCACA | T | 27 | a0001c0001t0001g0034a0001c0001t0001g0049a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+8276_279+8279d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | ||||||
chr6:109085626
|
G | A | 2 | a0001c0004t0005g0022a0001c0004t0005g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+8169C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085626 | ||||||
chr6:109085638
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.279+8157T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085638 | ||||||
chr6:109085693
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.279+8102C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085693 | ||||||
chr6:109086276
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+7519G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086276 | ||||||
chr6:109086304
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+7491T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086304 | ||||||
chr6:109086492
|
C | A | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+7303G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086492 | ||||||
chr6:109086655
|
T | G | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+7140A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086655 | ||||||
chr6:109086755
|
AATAACTA others(2): Show |
A | 53 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(50): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+7031_279+7039d others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086755 | ||||||
chr6:109086773
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+7022T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086773 | ||||||
chr6:109086900
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.279+6895C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086900 | ||||||
chr6:109086968
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6827G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086968 | ||||||
chr6:109087225
|
C | G | 27 | a0001c0001t0001g0034a0001c0001t0001g0049a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+6570G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087225 | ||||||
chr6:109087288
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6507A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087288 | ||||||
chr6:109087315
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6480C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087315 | ||||||
chr6:109087346
|
G | GA | 68 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0049others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.279+6448dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087346 | ||||||
chr6:109087399
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+6396T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087399 | ||||||
chr6:109087470
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0008g0050a0001c0001t0008g0051others(1): Show | 4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+6325T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087470 | ||||||
chr6:109087567
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6228A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087567 | ||||||
chr6:109087632
|
T | A | 5 | a0001c0001t0013g0015a0001c0004t0005g0020a0001c0004t0005g0021others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6163A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087632 | ||||||
chr6:109087817
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+5978G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087817 | ||||||
chr6:109087982
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+5813A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087982 | ||||||
chr6:109088071
|
A | G | 27 | a0001c0001t0001g0034a0001c0001t0001g0049a0002c0002t0002g0013others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+5724T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088071 | ||||||
chr6:109088146
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG01257.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.279+5649G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088146 | ||||||
chr6:109088510
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.279+5285A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088510 | ||||||
chr6:109088600
|
A | AT | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+5194dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088600 | ||||||
chr6:109089059
|
AT | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0132others(4): Show | 7 | HG02083.hp1 HG02109.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+4735delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089059 | ||||||
chr6:109089122
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+4673C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089122 | ||||||
chr6:109089256
|
G | A | 19 | a0001c0001t0001g0134a0001c0001t0003g0135a0001c0001t0003g0159others(16): Show | 19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+4539C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089256 | ||||||
chr6:109089293
|
C | T | 4 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+4502G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089293 | ||||||
chr6:109089366
|
T | C | 26 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(23): Show | 26 | HG00280.hp1 HG00438.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+4429A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089366 | ||||||
chr6:109089502
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+4293T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089502 | ||||||
chr6:109089586
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+4209C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089586 | ||||||
chr6:109089901
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3894G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089901 | ||||||
chr6:109090082
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3713G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090082 | ||||||
chr6:109090110
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+3685G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090110 | ||||||
chr6:109090507
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3288T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090507 | ||||||
chr6:109090547
|
A | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+3248T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090547 | ||||||
chr6:109090649
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.279+3146G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090649 | ||||||
chr6:109090685
|
G | A | 17 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(14): Show | 17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.279+3110C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090685 | ||||||
chr6:109090806
|
C | T | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279+2989G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090806 | ||||||
chr6:109090937
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2858A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090937 | ||||||
chr6:109091053
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+2742C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091053 | ||||||
chr6:109091172
|
C | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2623G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091172 | ||||||
chr6:109091251
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+2544C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091251 | ||||||
chr6:109091285
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.279+2510T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091285 | ||||||
chr6:109091356
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+2439C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091356 | ||||||
chr6:109091390
|
C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+2405G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091390 | ||||||
chr6:109091398
|
T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+2397A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091398 | ||||||
chr6:109091443
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+2352C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091443 | ||||||
chr6:109091507
|
T | C | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279+2288A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091507 | ||||||
chr6:109091539
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2256C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091539 | ||||||
chr6:109091573
|
C | T | 1 | a0001c0003t0004g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+2222G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091573 | ||||||
chr6:109091730
|
T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+2065A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091730 | ||||||
chr6:109091863
|
A | T | 2 | a0002c0002t0002g0013a0002c0002t0002g0014 | 2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.279+1932T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091863 | ||||||
chr6:109091895
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.279+1900T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091895 | ||||||
chr6:109092362
|
C | T | 2 | a0001c0005t0001g0008a0001c0005t0001g0009 | 2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.279+1433G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092362 | ||||||
chr6:109092572
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+1223G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092572 | ||||||
chr6:109092707
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0003g0181 | 2 | HG01109.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.279+1088C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092707 | ||||||
chr6:109093159
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+636A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093159 | ||||||
chr6:109093265
|
T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+530A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093265 | ||||||
chr6:109093279
|
A | G | 6 | a0001c0001t0010g0010a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+516T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093279 | ||||||
chr6:109093470
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+325C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093470 | ||||||
chr6:109093493
|
T | C | 1 | a0001c0003t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.279+302A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093493 | ||||||
chr6:109093504
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+291C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093504 |