geneid | 151011 |
---|---|
ensemblid | ENSG00000186522.15 |
hgncid | 14349 |
symbol | SEPTIN10 |
name | septin 10 |
refseq_nuc | NM_144710.5 |
refseq_prot | NP_653311.1 |
ensembl_nuc | ENST00000397712.7 |
ensembl_prot | ENSP00000380824.2 |
mane_status | MANE Select |
chr | chr2 |
start | 109542799 |
end | 109613966 |
strand | - |
ver | v1.2 |
region | chr2:109542799-109613966 |
region5000 | chr2:109537799-109618966 |
regionname0 | SEPTIN10_chr2_109542799_109613966 |
regionname5000 | SEPTIN10_chr2_109537799_109618966 |
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 | 454 | 398 | 97 | 73 | 167 | 14 | 45 | 127 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0002 | 0/0 | 454 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0003 | 0/0 | 454 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0004 | 0/0 | 454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0005 | 0/0 | 454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0006 | 0/0 | 454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
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 | 1365 | 392 | 91 | 73 | 167 | 14 | 45 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0002 | 0/0 | 1365 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0003 | 0/0 | 1365 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0004 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0005 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0006 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0007 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0008 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
c0009 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
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 | 1650 | 151 | 18 | 25 | 80 | 7 | 19 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0002 | 0/0 | 1650 | 97 | 26 | 15 | 34 | 4 | 18 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0003 | 0/0 | 1650 | 64 | 1 | 24 | 36 | 0 | 3 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0004 | 0/0 | 1650 | 61 | 33 | 8 | 16 | 3 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0005 | 0/0 | 1650 | 15 | 13 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0006 | 0/0 | 1650 | 8 | 3 | 0 | 1 | 0 | 4 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0007 | 0/0 | 1650 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0008 | 0/0 | 1650 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0009 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
t0010 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
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 | 3 | 0 | 2 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0372 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
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 | 1365 | 392 | 91 | 73 | 167 | 14 | 45 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0002 | 0/0 | 1365 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0007 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0008 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0002c0003 | 0/0 | 1365 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0003c0004 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0004c0006 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0005c0005 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0006c0009 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3014 | 149 | 18 | 25 | 78 | 7 | 19 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0002 | 0/0 | 3014 | 92 | 21 | 15 | 34 | 4 | 18 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0003 | 0/0 | 3014 | 64 | 1 | 24 | 36 | 0 | 3 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0004 | 0/0 | 3014 | 57 | 31 | 7 | 15 | 3 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0005 | 0/0 | 3014 | 15 | 13 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0006 | 0/0 | 3014 | 7 | 3 | 0 | 1 | 0 | 3 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0007 | 0/0 | 3014 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0008 | 0/0 | 3014 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0009 | 0/0 | 3014 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0001t0010 | 0/0 | 3014 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0002t0002 | 0/0 | 3014 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0007t0004 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0001c0008t0002 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0002c0003t0001 | 0/0 | 3014 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0003c0004t0006 | 0/0 | 3014 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0004c0006t0004 | 0/0 | 3014 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0005c0005t0004 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
a0006c0009t0004 | 0/0 | 3014 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | copy fasta | chr2 | 109537799 | 109618966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0372 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0009g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0007t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0001c0008t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0003c0004t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0004c0006t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0005c0005t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
a0006c0009t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | GBR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | GBR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0198 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0094 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0387 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0385 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0386 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02280 | hp1 | a0005 | c0005 | t0004 | g0219 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0337 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02970 | hp2 | a0001 | c0007 | t0004 | g0232 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0344 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03453 | hp1 | a0001 | c0008 | t0002 | g0089 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0161 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0343 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0136 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04199 | hp2 | a0003 | c0004 | t0006 | g0160 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0342 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18963 | hp1 | a0001 | c0001 | t0008 | g0311 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18984 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0388 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19066 | hp2 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19067 | hp1 | a0004 | c0006 | t0004 | g0194 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19075 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ASW | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ASW | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0184 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0384 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0105 | SAS | GIH | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0371 | SAS | GIH | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01123 | hp1 | a0006 | c0009 | t0004 | g0242 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0373 | REF | REF | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0372 | REF | REF | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:109546056
|
C | T | 1 | a0005 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1343G>A | p.Arg448His | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/11 | 1482/3014 | 1343/1365 | 448/454 | chr2 | 109546056 | ||
chr2:109546167
|
C | A | 1 | a0004 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.1232G>T | p.Arg411Ile | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/11 | 1371/3014 | 1232/1365 | 411/454 | chr2 | 109546167 | ||
chr2:109553137
|
C | T | 1 | a0003 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1111G>A | p.Val371Met | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/11 | 1250/3014 | 1111/1365 | 371/454 | chr2 | 109553137 | ||
chr2:109574615
|
A | G | 1 | a0002 | 2 | NA18969.hp2 NA18984.hp1 |
missense_variant | MODERATE | c.566T>C | p.Leu189Pro | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/11 | 705/3014 | 566/1365 | 189/454 | chr2 | 109574615 | ||
chr2:109613823
|
G | A | 1 | a0006 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.5C>T | p.Ala2Val | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/11 | 144/3014 | 5/1365 | 2/454 | chr2 | 109613823 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:109585212
|
T | C | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.327A>G | p.Thr109Thr | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/11 | 466/3014 | 327/1365 | 109/454 | chr2 | 109585212 | ||
chr2:109585749
|
T | C | 1 | a0001c0002 | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
synonymous_variant | LOW | c.189A>G | p.Gln63Gln | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/11 | 328/3014 | 189/1365 | 63/454 | chr2 | 109585749 | ||
chr2:109585827
|
G | A | 1 | a0001c0008 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.111C>T | p.Asn37Asn | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/11 | 250/3014 | 111/1365 | 37/454 | chr2 | 109585827 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:109542880
|
T | C | 1 | a0001c0001t0009 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1429 | chr2 | 109542880 | |||||
chr2:109542937
|
G | C | 1 | a0001c0001t0010 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1372 | chr2 | 109542937 | |||||
chr2:109543299
|
A | G | 1 | a0001c0001t0005 | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1010T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1010 | chr2 | 109543299 | |||||
chr2:109543406
|
C | A | 1 | a0001c0001t0003 | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*903G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 903 | chr2 | 109543406 | |||||
chr2:109543508
|
T | A | 5 | a0001c0001t0004a0001c0007t0004a0004c0006t0004others(2): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 801 | chr2 | 109543508 | |||||
chr2:109543529
|
T | C | 1 | a0001c0001t0008 | 2 | NA18963.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 780 | chr2 | 109543529 | |||||
chr2:109543830
|
A | G | 1 | a0001c0001t0003 | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*479T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 479 | chr2 | 109543830 | |||||
chr2:109543934
|
T | C | 1 | a0001c0001t0007 | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*375A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 375 | chr2 | 109543934 | |||||
chr2:109544015
|
G | A | 2 | a0001c0001t0006a0003c0004t0006 | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 294 | chr2 | 109544015 | |||||
chr2:109613916
|
A | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(10): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
5_prime_UTR_variant | MODIFIER | c.-89T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/11 | 89 | chr2 | 109613916 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:109544465
|
A | G | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1350-141T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544465 | ||||||
chr2:109544556
|
AG | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1350-233delC | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544556 | ||||||
chr2:109544614
|
T | A | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-290A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544614 | ||||||
chr2:109544615
|
G | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-291C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544615 | ||||||
chr2:109544786
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0152 | 3 | HG02027.hp1 NA18978.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1350-462G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544786 | ||||||
chr2:109544845
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1350-521T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544845 | ||||||
chr2:109544868
|
C | A | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350-544G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544868 | ||||||
chr2:109544869
|
C | T | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1350-545G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544869 | ||||||
chr2:109544886
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1350-562A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544886 | ||||||
chr2:109544887
|
G | A | 233 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(230): Show | 242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1350-563C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544887 | ||||||
chr2:109544901
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1350-577A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544901 | ||||||
chr2:109544906
|
G | A | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1350-582C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544906 | ||||||
chr2:109544927
|
A | C | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-603T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544927 | ||||||
chr2:109545137
|
T | A | 6 | a0001c0001t0005g0095a0001c0001t0005g0097a0001c0001t0005g0098others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-813A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545137 | ||||||
chr2:109545272
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1349+778C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545272 | ||||||
chr2:109545495
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1349+555G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545495 | ||||||
chr2:109545510
|
A | G | 1 | a0001c0001t0004g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1349+540T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545510 | ||||||
chr2:109545523
|
C | A | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1349+527G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545523 | ||||||
chr2:109545565
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1349+485G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545565 | ||||||
chr2:109545626
|
T | A | 1 | a0006c0009t0004g0242 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1349+424A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545626 | ||||||
chr2:109545649
|
C | T | 2 | a0001c0001t0004g0195a0001c0001t0004g0208 | 2 | NA18940.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1349+401G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545649 | ||||||
chr2:109545735
|
G | A | 28 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(25): Show | 28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1349+315C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545735 | ||||||
chr2:109545782
|
C | A | 5 | a0001c0001t0004g0233a0001c0001t0004g0234a0001c0001t0004g0235others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1349+268G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545782 | ||||||
chr2:109546247
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0316 | 2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1162-10T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546247 | ||||||
chr2:109546262
|
C | T | 2 | a0001c0001t0003g0033a0001c0001t0003g0035 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1162-25G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546262 | ||||||
chr2:109546299
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0244a0001c0001t0001g0247others(27): Show | 31 | HG00544.hp1 HG02027.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.1162-62C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546299 | ||||||
chr2:109546317
|
G | A | 4 | a0001c0001t0001g0373a0001c0001t0001g0375a0001c0001t0001g0380others(1): Show | 4 | HG00741.hp1 HG01106.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-80C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546317 | ||||||
chr2:109546499
|
C | T | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162-262G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546499 | ||||||
chr2:109546557
|
A | C | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1162-320T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546557 | ||||||
chr2:109546575
|
A | G | 1 | a0001c0001t0004g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1162-338T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546575 | ||||||
chr2:109546618
|
A | C | 2 | a0001c0001t0003g0023a0001c0001t0003g0055 | 2 | NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1162-381T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546618 | ||||||
chr2:109546847
|
T | C | 1 | a0001c0001t0006g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1162-610A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546847 | ||||||
chr2:109546900
|
T | G | 13 | a0001c0001t0003g0021a0001c0001t0003g0028a0001c0001t0003g0029others(10): Show | 13 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1162-663A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546900 | ||||||
chr2:109547091
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1162-854G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547091 | ||||||
chr2:109547113
|
T | C | 37 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0182others(34): Show | 38 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1162-876A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547113 | ||||||
chr2:109547369
|
G | GT | 104 | a0001c0001t0001g0010a0001c0001t0001g0247a0001c0001t0001g0252others(101): Show | 108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1162-1133dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | ||||||
chr2:109547369
|
G | GTT | 64 | a0001c0001t0001g0333a0001c0001t0002g0165a0001c0001t0003g0001others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1134_1162-113 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | ||||||
chr2:109547369
|
GT | G | 9 | a0001c0001t0001g0324a0001c0001t0001g0386a0001c0001t0004g0224others(6): Show | 9 | HG01175.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162-1133delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | ||||||
chr2:109547770
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-1533T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547770 | ||||||
chr2:109547928
|
C | A | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1162-1691G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547928 | ||||||
chr2:109548083
|
A | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1846T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548083 | ||||||
chr2:109548139
|
G | GA | 335 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(332): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1162-1903dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548139 | ||||||
chr2:109548177
|
CA | C | 232 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(229): Show | 241 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(238): Show |
intron_variant | MODIFIER | c.1162-1941delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548177 | ||||||
chr2:109548508
|
A | C | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.1162-2271T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548508 | ||||||
chr2:109548724
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162-2487G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548724 | ||||||
chr2:109548758
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-2521T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548758 | ||||||
chr2:109548763
|
T | G | 233 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(230): Show | 242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1162-2526A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548763 | ||||||
chr2:109548775
|
C | CA | 17 | a0001c0001t0001g0252a0001c0001t0001g0288a0001c0001t0001g0289others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1162-2539dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
C | CAA | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 86 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1162-2540_1162-253 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
C | CAAA | 12 | a0001c0001t0001g0244a0001c0001t0001g0297a0001c0001t0001g0308others(9): Show | 12 | HG00544.hp1 HG02056.hp2 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-2541_1162-253 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
CA | C | 52 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(49): Show | 55 | HG00609.hp1 HG00735.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.1162-2539delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
CAA | C | 48 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(45): Show | 49 | HG01255.hp1 HG01256.hp2 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.1162-2540_1162-253 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
CAAA | C | 55 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1162-2541_1162-253 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1162-2551_1162-253 others(17): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548775
|
CAAAAAAA others(7): Show |
C | 67 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(64): Show | 71 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1162-2552_1162-253 others(18): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | ||||||
chr2:109548848
|
A | G | 213 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0075others(210): Show | 221 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.1162-2611T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548848 | ||||||
chr2:109548930
|
C | G | 233 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(230): Show | 242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1162-2693G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548930 | ||||||
chr2:109548995
|
T | G | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1162-2758A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548995 | ||||||
chr2:109549348
|
A | T | 1 | a0001c0001t0001g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1162-3111T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549348 | ||||||
chr2:109549819
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1161+3268T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549819 | ||||||
chr2:109549897
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1161+3190G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549897 | ||||||
chr2:109549909
|
T | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1161+3178A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549909 | ||||||
chr2:109550057
|
G | A | 13 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(10): Show | 13 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161+3030C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550057 | ||||||
chr2:109550073
|
G | A | 60 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(57): Show | 62 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.1161+3014C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550073 | ||||||
chr2:109550238
|
T | G | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1161+2849A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550238 | ||||||
chr2:109550319
|
T | G | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2768A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550319 | ||||||
chr2:109550320
|
T | G | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161+2767A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550320 | ||||||
chr2:109550344
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1161+2743C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550344 | ||||||
chr2:109550533
|
C | G | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2554G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550533 | ||||||
chr2:109550572
|
C | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1161+2515G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550572 | ||||||
chr2:109550673
|
G | T | 1 | a0001c0008t0002g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1161+2414C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550673 | ||||||
chr2:109550674
|
A | T | 1 | a0001c0008t0002g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1161+2413T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550674 | ||||||
chr2:109550741
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161+2346A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550741 | ||||||
chr2:109550804
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161+2283G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550804 | ||||||
chr2:109551283
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0265a0001c0001t0001g0270 | 3 | HG01070.hp1 HG03486.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1161+1804A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551283 | ||||||
chr2:109551321
|
T | C | 22 | a0001c0001t0001g0010a0001c0001t0001g0252a0001c0001t0001g0255others(19): Show | 23 | HG00323.hp1 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1161+1766A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551321 | ||||||
chr2:109551432
|
C | T | 20 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(17): Show | 22 | HG00609.hp1 HG01934.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+1655G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551432 | ||||||
chr2:109551460
|
T | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1161+1627A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551460 | ||||||
chr2:109551641
|
T | A | 34 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0182others(31): Show | 35 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1161+1446A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551641 | ||||||
chr2:109551890
|
G | C | 19 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0075others(16): Show | 20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1161+1197C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551890 | ||||||
chr2:109551892
|
G | A | 2 | a0001c0001t0004g0233a0001c0001t0004g0237 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+1195C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551892 | ||||||
chr2:109551923
|
C | A | 5 | a0001c0001t0004g0233a0001c0001t0004g0234a0001c0001t0004g0235others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+1164G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551923 | ||||||
chr2:109551955
|
G | A | 82 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(79): Show | 85 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+1132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551955 | ||||||
chr2:109551957
|
G | A | 1 | a0003c0004t0006g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1161+1130C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551957 | ||||||
chr2:109551976
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1161+1111C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551976 | ||||||
chr2:109552160
|
G | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1161+927C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552160 | ||||||
chr2:109552202
|
G | A | 1 | a0001c0001t0004g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1161+885C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552202 | ||||||
chr2:109552398
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1161+689A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552398 | ||||||
chr2:109552473
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1161+614A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552473 | ||||||
chr2:109552532
|
G | A | 4 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0103others(1): Show | 5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+555C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552532 | ||||||
chr2:109552870
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1161+217T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552870 | ||||||
chr2:109552960
|
G | A | 2 | a0001c0001t0001g0349a0001c0001t0001g0365 | 2 | NA18989.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1161+127C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552960 | ||||||
chr2:109553034
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1161+53A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109553034 | ||||||
chr2:109553053
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1161+34T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109553053 | ||||||
chr2:109553409
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0250 | 2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1029-190A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553409 | ||||||
chr2:109553496
|
A | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-277T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553496 | ||||||
chr2:109553544
|
C | CA | 9 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(6): Show | 9 | HG01952.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-326dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553544 | ||||||
chr2:109553544
|
C | CAA | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-327_1029-326d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553544 | ||||||
chr2:109553588
|
C | T | 15 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-369G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553588 | ||||||
chr2:109553723
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1029-504C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553723 | ||||||
chr2:109553771
|
T | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0121 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1029-552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553771 | ||||||
chr2:109553810
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1029-591G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553810 | ||||||
chr2:109554106
|
T | C | 3 | a0001c0001t0004g0196a0001c0001t0004g0203a0001c0001t0004g0212 | 3 | NA18942.hp1 NA19062.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1029-887A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554106 | ||||||
chr2:109554316
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1029-1097C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554316 | ||||||
chr2:109554337
|
T | C | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1118A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554337 | ||||||
chr2:109554344
|
T | A | 1 | a0001c0001t0002g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1029-1125A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554344 | ||||||
chr2:109554417
|
T | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1198A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554417 | ||||||
chr2:109554569
|
G | A | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1350C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554569 | ||||||
chr2:109554829
|
C | G | 2 | a0001c0001t0003g0015a0001c0001t0003g0057 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1029-1610G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554829 | ||||||
chr2:109554834
|
C | A | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029-1615G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554834 | ||||||
chr2:109554974
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1029-1755C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554974 | ||||||
chr2:109555042
|
T | C | 2 | a0001c0001t0004g0192a0001c0001t0004g0209 | 2 | NA18945.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1029-1823A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555042 | ||||||
chr2:109555152
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1029-1933G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555152 | ||||||
chr2:109555238
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0313 | 2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1029-2019T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555238 | ||||||
chr2:109555620
|
T | C | 2 | a0001c0001t0002g0087a0001c0001t0002g0088 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1029-2401A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555620 | ||||||
chr2:109555624
|
G | A | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1029-2405C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555624 | ||||||
chr2:109555707
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0002g0141 | 2 | HG02027.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1029-2488G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555707 | ||||||
chr2:109555912
|
A | C | 214 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0075others(211): Show | 222 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(219): Show |
intron_variant | MODIFIER | c.1029-2693T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555912 | ||||||
chr2:109556078
|
A | C | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1029-2859T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556078 | ||||||
chr2:109556239
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1029-3020G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556239 | ||||||
chr2:109556244
|
A | G | 71 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(68): Show | 73 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1029-3025T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556244 | ||||||
chr2:109556519
|
GAACAGAT others(16): Show |
G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00621.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1029-3323_1029-330 others(27): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556519 | ||||||
chr2:109556584
|
C | T | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-3365G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556584 | ||||||
chr2:109556743
|
T | C | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029-3524A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556743 | ||||||
chr2:109556770
|
TAAA | T | 3 | a0001c0001t0004g0195a0001c0001t0004g0205a0001c0001t0004g0208 | 3 | NA18940.hp1 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1029-3554_1029-355 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556770 | ||||||
chr2:109556936
|
T | C | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1029-3717A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556936 | ||||||
chr2:109557144
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1029-3925G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557144 | ||||||
chr2:109557183
|
A | T | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(245): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1029-3964T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557183 | ||||||
chr2:109557184
|
A | T | 1 | a0001c0001t0003g0020 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1029-3965T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557184 | ||||||
chr2:109557286
|
A | G | 4 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0001g0259others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-4067T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557286 | ||||||
chr2:109557408
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1029-4189A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557408 | ||||||
chr2:109557631
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1029-4412T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557631 | ||||||
chr2:109557787
|
A | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1029-4568T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557787 | ||||||
chr2:109557851
|
C | CT | 67 | a0001c0001t0002g0126a0001c0001t0002g0173a0001c0001t0003g0001others(64): Show | 71 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1029-4633dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557851 | ||||||
chr2:109557851
|
C | CTT | 27 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(24): Show | 27 | HG00735.hp2 HG01106.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1029-4634_1029-463 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557851 | ||||||
chr2:109557927
|
G | T | 1 | a0001c0001t0002g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1029-4708C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557927 | ||||||
chr2:109558100
|
A | C | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-4881T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558100 | ||||||
chr2:109558113
|
A | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1029-4894T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558113 | ||||||
chr2:109558190
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1029-4971A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558190 | ||||||
chr2:109558293
|
C | T | 1 | a0001c0001t0003g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1029-5074G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558293 | ||||||
chr2:109558351
|
G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1029-5132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558351 | ||||||
chr2:109558429
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1029-5210G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558429 | ||||||
chr2:109558482
|
T | C | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-5263A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558482 | ||||||
chr2:109558631
|
G | A | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1029-5412C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558631 | ||||||
chr2:109558632
|
C | T | 3 | a0001c0001t0004g0195a0001c0001t0004g0205a0001c0001t0004g0208 | 3 | NA18940.hp1 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1029-5413G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558632 | ||||||
chr2:109558642
|
T | C | 4 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0103others(1): Show | 5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029-5423A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558642 | ||||||
chr2:109558708
|
C | T | 67 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(64): Show | 69 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.1029-5489G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558708 | ||||||
chr2:109558892
|
C | CT | 70 | a0001c0001t0002g0017a0001c0001t0002g0167a0001c0001t0002g0168others(67): Show | 71 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1028+5473dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558892 | ||||||
chr2:109558949
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1028+5417C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558949 | ||||||
chr2:109558969
|
T | G | 1 | a0001c0001t0001g0356 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1028+5397A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558969 | ||||||
chr2:109559013
|
A | G | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1028+5353T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559013 | ||||||
chr2:109559035
|
G | A | 60 | a0001c0001t0001g0319a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 62 | HG00140.hp2 HG00609.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1028+5331C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559035 | ||||||
chr2:109559054
|
T | C | 3 | a0001c0001t0003g0060a0001c0001t0003g0061a0001c0001t0003g0062 | 3 | HG02135.hp2 NA18984.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1028+5312A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559054 | ||||||
chr2:109559074
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0155 | 2 | NA18942.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1028+5292G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559074 | ||||||
chr2:109559466
|
C | A | 1 | a0001c0001t0002g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1028+4900G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559466 | ||||||
chr2:109559909
|
G | GT | 5 | a0001c0001t0004g0180a0001c0001t0004g0191a0001c0001t0004g0212others(2): Show | 5 | HG02622.hp2 NA18942.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4456_1028+445 others(5): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559909 | ||||||
chr2:109559910
|
C | T | 55 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0182others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1028+4456G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559910 | ||||||
chr2:109559911
|
C | CT | 130 | a0001c0001t0001g0256a0001c0001t0001g0316a0001c0001t0001g0323others(127): Show | 136 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.1028+4454dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | ||||||
chr2:109559911
|
C | CTT | 77 | a0001c0001t0002g0110a0001c0001t0002g0138a0001c0001t0002g0162others(74): Show | 79 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1028+4453_1028+445 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | ||||||
chr2:109559911
|
C | T | 5 | a0001c0001t0004g0180a0001c0001t0004g0191a0001c0001t0004g0212others(2): Show | 5 | HG02622.hp2 NA18942.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4455G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | ||||||
chr2:109559952
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1028+4414C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559952 | ||||||
chr2:109559973
|
T | C | 5 | a0001c0001t0001g0340a0001c0001t0007g0337a0001c0001t0007g0342others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4393A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559973 | ||||||
chr2:109559989
|
T | C | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+4377A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559989 | ||||||
chr2:109559997
|
C | T | 16 | a0001c0001t0003g0002a0001c0001t0003g0052a0001c0001t0005g0005others(13): Show | 18 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1028+4369G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559997 | ||||||
chr2:109560014
|
A | G | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+4352T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560014 | ||||||
chr2:109560040
|
C | A | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1028+4326G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560040 | ||||||
chr2:109560054
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1028+4312C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560054 | ||||||
chr2:109560077
|
C | T | 1 | a0004c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1028+4289G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560077 | ||||||
chr2:109560152
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0158 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1028+4214G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560152 | ||||||
chr2:109560210
|
G | C | 22 | a0001c0001t0004g0008a0001c0001t0004g0184a0001c0001t0004g0188others(19): Show | 23 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1028+4156C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560210 | ||||||
chr2:109560211
|
G | C | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1028+4155C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560211 | ||||||
chr2:109560312
|
C | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+4054G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560312 | ||||||
chr2:109560408
|
C | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1028+3958G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560408 | ||||||
chr2:109560532
|
T | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+3834A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560532 | ||||||
chr2:109560672
|
C | T | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1028+3694G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560672 | ||||||
chr2:109560692
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028+3674C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560692 | ||||||
chr2:109560749
|
C | T | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028+3617G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560749 | ||||||
chr2:109560796
|
A | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1028+3570T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560796 | ||||||
chr2:109561017
|
T | G | 235 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(232): Show | 244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.1028+3349A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561017 | ||||||
chr2:109561068
|
TC | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0094others(10): Show | 14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028+3297delG | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561068 | ||||||
chr2:109561145
|
G | A | 1 | a0001c0001t0004g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1028+3221C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561145 | ||||||
chr2:109561314
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1028+3052G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561314 | ||||||
chr2:109561342
|
C | T | 2 | a0001c0001t0004g0216a0001c0001t0004g0217 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1028+3024G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561342 | ||||||
chr2:109561482
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1028+2884G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561482 | ||||||
chr2:109561724
|
A | G | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+2642T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561724 | ||||||
chr2:109561756
|
G | A | 1 | a0001c0001t0001g0370 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1028+2610C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561756 | ||||||
chr2:109561971
|
TCAAGGCC others(15): Show |
T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+2373_1028+239 others(26): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561971 | ||||||
chr2:109562058
|
C | A | 1 | a0001c0001t0005g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1028+2308G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562058 | ||||||
chr2:109562110
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1028+2256C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562110 | ||||||
chr2:109562128
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1028+2238C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562128 | ||||||
chr2:109562169
|
T | G | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1028+2197A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562169 | ||||||
chr2:109562215
|
AAATAAT | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1028+2145_1028+215 others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562215 | ||||||
chr2:109562498
|
G | A | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.1028+1868C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562498 | ||||||
chr2:109562530
|
TA | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+1835delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562530 | ||||||
chr2:109562674
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1028+1692C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562674 | ||||||
chr2:109562904
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1028+1462G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562904 | ||||||
chr2:109562906
|
CA | C | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1028+1459delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562906 | ||||||
chr2:109562911
|
C | CT | 59 | a0001c0001t0001g0312a0001c0001t0003g0001a0001c0001t0003g0002others(56): Show | 62 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1028+1454dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562911 | ||||||
chr2:109562911
|
C | CTT | 6 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0027others(3): Show | 7 | HG01255.hp2 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028+1453_1028+145 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562911 | ||||||
chr2:109562924
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1028+1442A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562924 | ||||||
chr2:109562942
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1028+1424C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562942 | ||||||
chr2:109562964
|
G | A | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+1402C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562964 | ||||||
chr2:109563040
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1028+1326T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563040 | ||||||
chr2:109563208
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028+1158C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563208 | ||||||
chr2:109563333
|
T | C | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1028+1033A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563333 | ||||||
chr2:109563494
|
C | T | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1028+872G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563494 | ||||||
chr2:109563653
|
A | G | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1028+713T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563653 | ||||||
chr2:109564020
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1028+346A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564020 | ||||||
chr2:109564071
|
G | T | 1 | a0004c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1028+295C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564071 | ||||||
chr2:109564110
|
CAG | C | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1028+254_1028+255d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564110 | ||||||
chr2:109564128
|
C | T | 4 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0183others(1): Show | 4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028+238G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564128 | ||||||
chr2:109564140
|
T | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+226A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564140 | ||||||
chr2:109564226
|
T | TA | 37 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0182others(34): Show | 38 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1028+139dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564226 | ||||||
chr2:109564233
|
T | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | NA18963.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1028+133A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564233 | ||||||
chr2:109564253
|
A | G | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028+113T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564253 | ||||||
chr2:109564361
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1028+5G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564361 | ||||||
chr2:109564540
|
C | CA | 5 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0272others(2): Show | 5 | HG00423.hp2 NA18960.hp2 NA18962.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.860-7dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564540 | ||||||
chr2:109564659
|
A | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.860-125T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564659 | ||||||
chr2:109564768
|
G | C | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.860-234C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564768 | ||||||
chr2:109564915
|
G | A | 3 | a0001c0001t0004g0234a0001c0001t0004g0235a0001c0001t0004g0236 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.860-381C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564915 | ||||||
chr2:109564967
|
T | C | 23 | a0001c0001t0004g0008a0001c0001t0004g0184a0001c0001t0004g0188others(20): Show | 24 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.860-433A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564967 | ||||||
chr2:109565020
|
T | A | 1 | a0001c0001t0004g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.860-486A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565020 | ||||||
chr2:109565060
|
T | C | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.860-526A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565060 | ||||||
chr2:109565074
|
C | T | 6 | a0001c0001t0002g0112a0001c0001t0002g0117a0001c0001t0002g0124others(3): Show | 6 | HG01516.hp2 HG01517.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.860-540G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565074 | ||||||
chr2:109565127
|
G | C | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-593C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565127 | ||||||
chr2:109565239
|
C | T | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.859+524G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565239 | ||||||
chr2:109565294
|
A | T | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+469T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565294 | ||||||
chr2:109565390
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.859+373T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565390 | ||||||
chr2:109565412
|
C | A | 1 | a0001c0001t0004g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.859+351G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565412 | ||||||
chr2:109565432
|
A | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.859+331T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565432 | ||||||
chr2:109565433
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.859+330A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565433 | ||||||
chr2:109565575
|
T | A | 29 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(26): Show | 30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.859+188A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565575 | ||||||
chr2:109565733
|
A | G | 2 | a0001c0001t0004g0222a0001c0001t0004g0231 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.859+30T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565733 | ||||||
chr2:109565885
|
T | G | 2 | a0001c0001t0005g0097a0001c0001t0005g0098 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.763-26A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565885 | ||||||
chr2:109565943
|
ATAAT | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.763-88_763-85delAT others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565943 | ||||||
chr2:109565985
|
G | A | 1 | a0001c0001t0004g0191 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.763-126C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565985 | ||||||
chr2:109566117
|
A | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(232): Show | 244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.763-258T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566117 | ||||||
chr2:109566156
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.763-297A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566156 | ||||||
chr2:109566160
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.763-301C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566160 | ||||||
chr2:109566292
|
T | G | 3 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226 | 3 | HG02451.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.763-433A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566292 | ||||||
chr2:109566310
|
G | A | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.763-451C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566310 | ||||||
chr2:109566312
|
C | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.763-453G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566312 | ||||||
chr2:109566442
|
G | A | 4 | a0001c0001t0004g0192a0001c0001t0004g0209a0001c0001t0004g0210others(1): Show | 4 | NA18945.hp2 NA18962.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-583C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566442 | ||||||
chr2:109566493
|
T | C | 18 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(15): Show | 18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.763-634A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566493 | ||||||
chr2:109566564
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.763-705A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566564 | ||||||
chr2:109566613
|
A | G | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.763-754T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566613 | ||||||
chr2:109566661
|
G | A | 1 | a0001c0001t0004g0189 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.763-802C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566661 | ||||||
chr2:109566703
|
C | G | 347 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(344): Show | 360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.763-844G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566703 | ||||||
chr2:109566776
|
C | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.763-917G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566776 | ||||||
chr2:109566896
|
T | G | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.762+919A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566896 | ||||||
chr2:109567016
|
G | GT | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.762+798dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567016 | ||||||
chr2:109567208
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.762+607C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567208 | ||||||
chr2:109567459
|
C | A | 67 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(64): Show | 69 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.762+356G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567459 | ||||||
chr2:109567463
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.762+352G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567463 | ||||||
chr2:109567696
|
A | G | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.762+119T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567696 | ||||||
chr2:109568116
|
C | T | 3 | a0001c0001t0003g0054a0001c0001t0003g0065a0001c0001t0003g0067 | 3 | HG00609.hp2 NA18961.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.601-140G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568116 | ||||||
chr2:109568373
|
C | CT | 68 | a0001c0001t0001g0261a0001c0001t0001g0309a0001c0001t0001g0317others(65): Show | 68 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.601-398dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568373 | ||||||
chr2:109568404
|
C | T | 4 | a0001c0001t0001g0373a0001c0001t0001g0375a0001c0001t0001g0380others(1): Show | 4 | HG00741.hp1 HG01106.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-428G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568404 | ||||||
chr2:109568466
|
G | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-490C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568466 | ||||||
chr2:109568670
|
G | GCCT | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.601-697_601-695dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568670 | ||||||
chr2:109568757
|
G | C | 2 | a0001c0001t0001g0296a0001c0001t0001g0315 | 2 | NA18943.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.601-781C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568757 | ||||||
chr2:109568860
|
C | T | 5 | a0001c0001t0001g0340a0001c0001t0007g0337a0001c0001t0007g0342others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-884G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568860 | ||||||
chr2:109568868
|
T | C | 23 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(20): Show | 23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.601-892A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568868 | ||||||
chr2:109568878
|
T | C | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.601-902A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568878 | ||||||
chr2:109569192
|
G | A | 12 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-1216C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569192 | ||||||
chr2:109569237
|
T | A | 1 | a0001c0001t0001g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601-1261A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569237 | ||||||
chr2:109569300
|
A | G | 2 | a0001c0001t0007g0343a0001c0001t0007g0344 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.601-1324T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569300 | ||||||
chr2:109569379
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0264a0001c0001t0001g0282others(3): Show | 7 | HG01261.hp1 HG01358.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-1403G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569379 | ||||||
chr2:109569387
|
C | T | 1 | a0001c0001t0004g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.601-1411G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569387 | ||||||
chr2:109569437
|
T | TA | 44 | a0001c0001t0001g0009a0001c0001t0001g0244a0001c0001t0001g0247others(41): Show | 45 | HG00544.hp1 HG00639.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-1462dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | ||||||
chr2:109569437
|
TA | T | 100 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(97): Show | 104 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(101): Show |
intron_variant | MODIFIER | c.601-1462delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | ||||||
chr2:109569437
|
TAA | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-1463_601-1462d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | ||||||
chr2:109569439
|
A | C | 1 | a0001c0001t0004g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.601-1463T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569439 | ||||||
chr2:109569513
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.601-1537C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569513 | ||||||
chr2:109569589
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.601-1613C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569589 | ||||||
chr2:109569847
|
G | GT | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-1872dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569847 | ||||||
chr2:109569857
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0316 | 2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.601-1881T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569857 | ||||||
chr2:109569938
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.601-1962T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569938 | ||||||
chr2:109570027
|
C | CA | 39 | a0001c0001t0001g0266a0001c0001t0002g0155a0001c0001t0004g0008others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.601-2052dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570027 | ||||||
chr2:109570061
|
G | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-2085C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570061 | ||||||
chr2:109570091
|
G | A | 1 | a0001c0001t0001g0373 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.601-2115C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570091 | ||||||
chr2:109570156
|
G | A | 5 | a0001c0001t0004g0193a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG01192.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-2180C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570156 | ||||||
chr2:109570175
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.601-2199A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570175 | ||||||
chr2:109570188
|
A | G | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-2212T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570188 | ||||||
chr2:109570527
|
G | GT | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(103): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.601-2552dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570527 | ||||||
chr2:109570527
|
GT | G | 35 | a0001c0001t0004g0008a0001c0001t0004g0182a0001c0001t0004g0183others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.601-2552delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570527 | ||||||
chr2:109570605
|
ACCTCCGC others(22): Show |
A | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-2658_601-2630d others(31): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570605 | ||||||
chr2:109570781
|
G | C | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-2805C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570781 | ||||||
chr2:109570996
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.601-3020C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570996 | ||||||
chr2:109571024
|
C | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-3048G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571024 | ||||||
chr2:109571130
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-3154G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571130 | ||||||
chr2:109571282
|
C | T | 28 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(25): Show | 28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.600+3299G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571282 | ||||||
chr2:109571290
|
T | C | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.600+3291A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571290 | ||||||
chr2:109571398
|
C | A | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.600+3183G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571398 | ||||||
chr2:109571523
|
A | T | 1 | a0001c0001t0003g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.600+3058T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571523 | ||||||
chr2:109571527
|
C | G | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.600+3054G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571527 | ||||||
chr2:109571588
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.600+2993T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571588 | ||||||
chr2:109571645
|
G | A | 233 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(230): Show | 242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.600+2936C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571645 | ||||||
chr2:109571808
|
C | A | 2 | a0001c0001t0006g0133a0001c0001t0006g0135 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.600+2773G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571808 | ||||||
chr2:109571871
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0142 | 2 | NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.600+2710T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571871 | ||||||
chr2:109571884
|
G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.600+2697C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571884 | ||||||
chr2:109571950
|
A | G | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.600+2631T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571950 | ||||||
chr2:109572582
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+1999C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572582 | ||||||
chr2:109572609
|
C | CT | 45 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0001g0272others(42): Show | 45 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.600+1971dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | ||||||
chr2:109572609
|
CT | C | 28 | a0001c0001t0001g0339a0001c0001t0001g0362a0001c0001t0001g0374others(25): Show | 29 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.600+1971delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | ||||||
chr2:109572609
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+1961_600+1971d others(13): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | ||||||
chr2:109572653
|
G | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0252a0001c0001t0001g0255others(19): Show | 23 | HG00323.hp1 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+1928C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572653 | ||||||
chr2:109572666
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.600+1915C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572666 | ||||||
chr2:109572885
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.600+1696C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572885 | ||||||
chr2:109573069
|
G | T | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.600+1512C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573069 | ||||||
chr2:109573343
|
T | A | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.600+1238A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573343 | ||||||
chr2:109573515
|
C | T | 11 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(8): Show | 12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+1066G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573515 | ||||||
chr2:109573561
|
A | G | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+1020T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573561 | ||||||
chr2:109573562
|
A | C | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+1019T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573562 | ||||||
chr2:109573785
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.600+796C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573785 | ||||||
chr2:109573959
|
G | A | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.600+622C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573959 | ||||||
chr2:109574056
|
A | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0250a0001c0001t0001g0330 | 3 | HG03704.hp1 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.600+525T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574056 | ||||||
chr2:109574088
|
T | C | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.600+493A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574088 | ||||||
chr2:109574198
|
A | G | 235 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(232): Show | 244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.600+383T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574198 | ||||||
chr2:109574204
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.600+377G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574204 | ||||||
chr2:109574310
|
G | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+271C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574310 | ||||||
chr2:109574404
|
C | A | 1 | a0001c0001t0004g0189 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.600+177G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574404 | ||||||
chr2:109574443
|
T | TA | 48 | a0001c0001t0001g0361a0001c0001t0002g0006a0001c0001t0002g0007others(45): Show | 51 | HG00609.hp1 HG01257.hp1 HG01258.hp2 others(48): Show |
intron_variant | MODIFIER | c.600+137dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574443
|
T | TAA | 39 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0109others(36): Show | 39 | HG00735.hp2 HG01069.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.600+136_600+137dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574443
|
T | TAAA | 55 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(52): Show | 59 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.600+135_600+137dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574443
|
TA | T | 129 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.600+137delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574443
|
TAA | T | 27 | a0001c0001t0001g0252a0001c0001t0001g0266a0001c0001t0001g0277others(24): Show | 27 | HG00639.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.600+136_600+137del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574443
|
TAAA | T | 35 | a0001c0001t0004g0008a0001c0001t0004g0182a0001c0001t0004g0183others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.600+135_600+137del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | ||||||
chr2:109574448
|
A | T | 3 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0231 | 3 | HG02109.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+133T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574448 | ||||||
chr2:109574467
|
T | A | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+114A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574467 | ||||||
chr2:109574470
|
A | T | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+111T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574470 | ||||||
chr2:109574553
|
G | C | 57 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(54): Show | 58 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.600+28C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574553 | ||||||
chr2:109574553
|
G | T | 3 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226 | 3 | HG02451.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.600+28C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574553 | ||||||
chr2:109574565
|
C | T | 29 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(26): Show | 30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.600+16G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574565 | ||||||
chr2:109574908
|
T | TA | 9 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-142dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574908 | ||||||
chr2:109574908
|
TA | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0103others(1): Show | 5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-142delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574908 | ||||||
chr2:109574979
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.414-212A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574979 | ||||||
chr2:109575289
|
T | C | 1 | a0001c0001t0001g0368 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.414-522A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575289 | ||||||
chr2:109575351
|
A | G | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.414-584T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575351 | ||||||
chr2:109575372
|
T | G | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.414-605A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575372 | ||||||
chr2:109575434
|
A | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-667T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575434 | ||||||
chr2:109575678
|
C | G | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-911G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575678 | ||||||
chr2:109575692
|
C | T | 19 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0075others(16): Show | 20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-925G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575692 | ||||||
chr2:109575840
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-1073C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575840 | ||||||
chr2:109575860
|
T | C | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.414-1093A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575860 | ||||||
chr2:109576269
|
A | AAT | 3 | a0001c0001t0001g0288a0001c0001t0002g0084a0001c0001t0002g0085 | 3 | HG02976.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.414-1504_414-1503d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576269 | ||||||
chr2:109576271
|
T | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-1504A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576271 | ||||||
chr2:109576619
|
A | T | 3 | a0001c0001t0003g0054a0001c0001t0003g0065a0001c0001t0003g0067 | 3 | HG00609.hp2 NA18961.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.414-1852T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576619 | ||||||
chr2:109576781
|
C | A | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.414-2014G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576781 | ||||||
chr2:109576783
|
C | G | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2016G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576783 | ||||||
chr2:109576808
|
A | G | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-2041T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576808 | ||||||
chr2:109576860
|
A | G | 2 | a0001c0001t0004g0233a0001c0001t0004g0237 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2093T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576860 | ||||||
chr2:109576884
|
G | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG02165.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.414-2117C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576884 | ||||||
chr2:109576967
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.414-2200A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576967 | ||||||
chr2:109577095
|
G | A | 4 | a0001c0001t0001g0334a0001c0001t0002g0215a0002c0003t0001g0286others(1): Show | 4 | HG04204.hp2 NA18969.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-2328C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577095 | ||||||
chr2:109577314
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2547G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577314 | ||||||
chr2:109577318
|
C | T | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-2551G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577318 | ||||||
chr2:109577319
|
G | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-2552C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577319 | ||||||
chr2:109577598
|
T | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.414-2831A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | ||||||
chr2:109577598
|
T | TA | 26 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0109others(23): Show | 26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.414-2832dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | ||||||
chr2:109577598
|
TA | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0345others(4): Show | 7 | HG01168.hp2 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2832delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | ||||||
chr2:109577613
|
G | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-2846C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577613 | ||||||
chr2:109577801
|
T | C | 1 | a0001c0001t0004g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.414-3034A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577801 | ||||||
chr2:109577857
|
G | A | 1 | a0001c0001t0006g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.414-3090C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577857 | ||||||
chr2:109577861
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.414-3094G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577861 | ||||||
chr2:109577912
|
C | CA | 24 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(21): Show | 24 | HG01167.hp2 HG01169.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.414-3146dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | ||||||
chr2:109577912
|
CA | C | 111 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.414-3146delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | ||||||
chr2:109577912
|
CAA | C | 81 | a0001c0001t0001g0266a0001c0001t0001g0325a0001c0001t0001g0334others(78): Show | 84 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-3147_414-3146d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | ||||||
chr2:109577912
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0216a0001c0001t0004g0217 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.414-3156_414-3146d others(13): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | ||||||
chr2:109578061
|
G | T | 5 | a0001c0001t0003g0019a0001c0001t0003g0043a0001c0001t0003g0059others(2): Show | 5 | NA18947.hp1 NA18949.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-3294C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578061 | ||||||
chr2:109578111
|
C | G | 2 | a0001c0001t0005g0097a0001c0001t0005g0098 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.414-3344G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578111 | ||||||
chr2:109578238
|
A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0315 | 3 | NA18943.hp2 NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.414-3471T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578238 | ||||||
chr2:109578299
|
G | T | 2 | a0001c0001t0004g0206a0001c0001t0004g0241 | 2 | HG02074.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.414-3532C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578299 | ||||||
chr2:109578466
|
A | C | 61 | a0001c0001t0001g0386a0001c0001t0004g0008a0001c0001t0004g0180others(58): Show | 62 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.414-3699T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578466 | ||||||
chr2:109578542
|
GA | G | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.414-3776delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578542 | ||||||
chr2:109578584
|
G | T | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.414-3817C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578584 | ||||||
chr2:109578624
|
C | T | 1 | a0001c0001t0001g0349 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.414-3857G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578624 | ||||||
chr2:109578690
|
C | T | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-3923G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578690 | ||||||
chr2:109578703
|
G | T | 10 | a0001c0001t0002g0006a0001c0001t0002g0145a0001c0001t0002g0146others(7): Show | 11 | HG00609.hp1 HG02040.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-3936C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578703 | ||||||
chr2:109579142
|
T | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-4375A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579142 | ||||||
chr2:109579214
|
A | C | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4447T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579214 | ||||||
chr2:109579303
|
C | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4536G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579303 | ||||||
chr2:109579343
|
T | C | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4576A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579343 | ||||||
chr2:109579433
|
G | T | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.414-4666C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579433 | ||||||
chr2:109579462
|
C | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0184a0001c0001t0004g0188others(2): Show | 6 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-4695G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579462 | ||||||
chr2:109579653
|
G | A | 1 | a0001c0001t0003g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.414-4886C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579653 | ||||||
chr2:109579665
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.414-4898C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579665 | ||||||
chr2:109579892
|
G | A | 5 | a0001c0001t0002g0107a0001c0001t0002g0118a0001c0001t0002g0119others(2): Show | 5 | NA18963.hp2 NA18971.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-5125C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579892 | ||||||
chr2:109579947
|
C | G | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+5179G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579947 | ||||||
chr2:109579994
|
G | A | 27 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(24): Show | 28 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+5132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579994 | ||||||
chr2:109580180
|
G | T | 2 | a0002c0003t0001g0286a0002c0003t0001g0287 | 2 | NA18969.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.413+4946C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580180 | ||||||
chr2:109580181
|
C | CA | 61 | a0001c0001t0002g0129a0001c0001t0003g0068a0001c0001t0004g0008others(58): Show | 62 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.413+4944dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580181 | ||||||
chr2:109580272
|
G | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4854C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580272 | ||||||
chr2:109580326
|
A | G | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+4800T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580326 | ||||||
chr2:109580349
|
C | CA | 7 | a0001c0001t0001g0375a0001c0001t0001g0376a0001c0001t0002g0171others(4): Show | 7 | HG01106.hp2 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+4776dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | ||||||
chr2:109580349
|
CA | C | 200 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(197): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.413+4776delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | ||||||
chr2:109580349
|
CAA | C | 52 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(49): Show | 53 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.413+4775_413+4776d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | ||||||
chr2:109580372
|
G | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4754C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580372 | ||||||
chr2:109580474
|
CA | C | 18 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(15): Show | 18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+4651delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580474 | ||||||
chr2:109580589
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.413+4537G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580589 | ||||||
chr2:109580632
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.413+4494T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580632 | ||||||
chr2:109580820
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.413+4306A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580820 | ||||||
chr2:109580875
|
C | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4251G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580875 | ||||||
chr2:109581105
|
C | T | 1 | a0001c0001t0005g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+4021G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581105 | ||||||
chr2:109581274
|
T | C | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+3852A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581274 | ||||||
chr2:109581319
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+3807G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581319 | ||||||
chr2:109581339
|
A | C | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.413+3787T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581339 | ||||||
chr2:109581501
|
T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413+3625A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581501 | ||||||
chr2:109581528
|
G | GA | 71 | a0001c0001t0001g0321a0001c0001t0001g0354a0001c0001t0001g0355others(68): Show | 75 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.413+3597dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581528 | ||||||
chr2:109581761
|
C | G | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+3365G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581761 | ||||||
chr2:109581763
|
G | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+3363C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581763 | ||||||
chr2:109582007
|
C | T | 1 | a0001c0001t0004g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+3119G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582007 | ||||||
chr2:109582046
|
G | A | 205 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(202): Show | 213 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.413+3080C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582046 | ||||||
chr2:109582075
|
G | GAC | 13 | a0001c0001t0001g0354a0001c0001t0001g0389a0001c0001t0002g0084others(10): Show | 14 | HG00735.hp1 HG01433.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+3049_413+3050d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
G | GACAC | 6 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(3): Show | 6 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+3047_413+3050d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
G | GACACAC | 4 | a0001c0001t0005g0095a0001c0001t0005g0096a0001c0001t0005g0100others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+3045_413+3050d others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GAC | G | 23 | a0001c0001t0001g0386a0001c0001t0002g0004a0001c0001t0002g0074others(20): Show | 24 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+3049_413+3050d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACAC | G | 33 | a0001c0001t0001g0253a0001c0001t0001g0352a0001c0001t0001g0362others(30): Show | 35 | HG00597.hp2 HG00609.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.413+3047_413+3050d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACACAC | G | 9 | a0001c0001t0001g0313a0001c0001t0001g0327a0001c0001t0001g0336others(6): Show | 9 | HG01243.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+3045_413+3050d others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACACACA others(1): Show |
G | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.413+3043_413+3050d others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACACACA others(3): Show |
G | 54 | a0001c0001t0001g0249a0001c0001t0001g0272a0001c0001t0001g0274others(51): Show | 55 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.413+3041_413+3050d others(12): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACACACA others(5): Show |
G | 7 | a0001c0001t0001g0295a0001c0001t0001g0316a0001c0001t0001g0338others(4): Show | 7 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+3039_413+3050d others(14): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582075
|
GACACACA others(7): Show |
G | 69 | a0001c0001t0001g0346a0001c0001t0001g0355a0001c0001t0001g0358others(66): Show | 73 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.413+3037_413+3050d others(16): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | ||||||
chr2:109582110
|
A | ACACT | 3 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0128 | 3 | HG01981.hp1 HG02886.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.413+3012_413+3015d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | ||||||
chr2:109582110
|
A | ACT | 16 | a0001c0001t0002g0106a0001c0001t0002g0110a0001c0001t0002g0111others(13): Show | 16 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+3015_413+3016i others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | ||||||
chr2:109582110
|
A | T | 7 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0112others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+3016T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | ||||||
chr2:109582184
|
A | T | 1 | a0001c0001t0004g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.413+2942T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582184 | ||||||
chr2:109582218
|
C | T | 6 | a0001c0001t0003g0002a0001c0001t0003g0026a0001c0001t0003g0052others(3): Show | 7 | HG02080.hp2 HG02135.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+2908G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582218 | ||||||
chr2:109582304
|
C | T | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+2822G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582304 | ||||||
chr2:109582389
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.413+2737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582389 | ||||||
chr2:109582466
|
C | T | 4 | a0001c0001t0007g0337a0001c0001t0007g0342a0001c0001t0007g0343others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+2660G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582466 | ||||||
chr2:109582520
|
C | T | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413+2606G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582520 | ||||||
chr2:109582873
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.413+2253C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582873 | ||||||
chr2:109582922
|
T | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2204A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582922 | ||||||
chr2:109582976
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.413+2150A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582976 | ||||||
chr2:109582985
|
A | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2141T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582985 | ||||||
chr2:109583040
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.413+2086T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583040 | ||||||
chr2:109583175
|
TTAAAC | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1946_413+1950d others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583175 | ||||||
chr2:109583292
|
T | G | 1 | a0001c0001t0005g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413+1834A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583292 | ||||||
chr2:109583355
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+1771A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583355 | ||||||
chr2:109583389
|
G | A | 27 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(24): Show | 28 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+1737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583389 | ||||||
chr2:109583440
|
A | G | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.413+1686T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583440 | ||||||
chr2:109583592
|
G | C | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+1534C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583592 | ||||||
chr2:109583643
|
T | A | 3 | a0001c0001t0004g0218a0001c0001t0004g0220a0001c0001t0004g0221 | 3 | HG02109.hp1 HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.413+1483A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583643 | ||||||
chr2:109583751
|
C | T | 12 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+1375G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583751 | ||||||
chr2:109583807
|
T | A | 7 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226others(4): Show | 7 | HG01175.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1319A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583807 | ||||||
chr2:109584008
|
C | G | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.413+1118G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584008 | ||||||
chr2:109584011
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.413+1115A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584011 | ||||||
chr2:109584122
|
G | A | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0335 | 3 | NA18945.hp1 NA18956.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.413+1004C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584122 | ||||||
chr2:109584203
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413+923C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584203 | ||||||
chr2:109584215
|
G | A | 10 | a0001c0001t0002g0017a0001c0001t0002g0167a0001c0001t0002g0168others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+911C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584215 | ||||||
chr2:109584301
|
A | AC | 336 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(333): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.413+824dupG | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584301 | ||||||
chr2:109584323
|
A | C | 1 | a0001c0001t0004g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+803T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584323 | ||||||
chr2:109584474
|
C | CA | 161 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0312others(158): Show | 168 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(165): Show |
intron_variant | MODIFIER | c.413+651dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | ||||||
chr2:109584474
|
C | CAA | 59 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0075others(56): Show | 61 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.413+650_413+651dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | ||||||
chr2:109584474
|
C | CAAA | 15 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0081others(12): Show | 15 | HG01192.hp2 HG01884.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+649_413+651dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | ||||||
chr2:109584474
|
CA | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0293a0001c0001t0001g0294others(4): Show | 7 | HG00323.hp1 HG01192.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+651delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | ||||||
chr2:109584611
|
C | T | 12 | a0001c0001t0001g0346a0001c0001t0001g0358a0001c0001t0001g0359others(9): Show | 12 | HG00544.hp2 HG01243.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+515G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584611 | ||||||
chr2:109584840
|
T | A | 1 | a0001c0001t0001g0384 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.413+286A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584840 | ||||||
chr2:109584844
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.413+282G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584844 | ||||||
chr2:109585107
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.413+19T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109585107 | ||||||
chr2:109585493
|
G | C | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.218-172C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585493 | ||||||
chr2:109585530
|
A | G | 5 | a0001c0001t0004g0233a0001c0001t0004g0234a0001c0001t0004g0235others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+191T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585530 | ||||||
chr2:109585541
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0313 | 2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.217+180A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585541 | ||||||
chr2:109585547
|
G | T | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.217+174C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585547 | ||||||
chr2:109585942
|
T | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-104A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109585942 | ||||||
chr2:109585978
|
G | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-140C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109585978 | ||||||
chr2:109586336
|
G | T | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.100-498C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586336 | ||||||
chr2:109586390
|
G | C | 2 | a0001c0001t0006g0161a0003c0004t0006g0160 | 2 | HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.100-552C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586390 | ||||||
chr2:109586405
|
C | T | 10 | a0001c0001t0002g0017a0001c0001t0002g0167a0001c0001t0002g0168others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-567G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586405 | ||||||
chr2:109586426
|
CT | C | 60 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.100-589delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586426 | ||||||
chr2:109586586
|
A | G | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-748T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586586 | ||||||
chr2:109586589
|
C | A | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-751G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586589 | ||||||
chr2:109586658
|
T | C | 6 | a0001c0001t0002g0017a0001c0001t0004g0233a0001c0001t0004g0234others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-820A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586658 | ||||||
chr2:109586995
|
C | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-1157G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586995 | ||||||
chr2:109587180
|
A | G | 12 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(9): Show | 12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-1342T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587180 | ||||||
chr2:109587312
|
T | A | 1 | a0001c0001t0002g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-1474A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587312 | ||||||
chr2:109587390
|
T | C | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587390 | ||||||
chr2:109587406
|
T | C | 75 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-1568A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587406 | ||||||
chr2:109587684
|
C | T | 81 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(78): Show | 84 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(81): Show |
intron_variant | MODIFIER | c.100-1846G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587684 | ||||||
chr2:109587837
|
T | C | 4 | a0001c0001t0004g0193a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG01192.hp2 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-1999A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587837 | ||||||
chr2:109587913
|
C | CA | 32 | a0001c0001t0001g0276a0001c0001t0001g0314a0001c0001t0001g0332others(29): Show | 32 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.100-2076dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587913 | ||||||
chr2:109587932
|
A | G | 35 | a0001c0001t0004g0008a0001c0001t0004g0181a0001c0001t0004g0182others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.100-2094T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587932 | ||||||
chr2:109587957
|
G | A | 65 | a0001c0001t0002g0145a0001c0001t0003g0001a0001c0001t0003g0002others(62): Show | 69 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.100-2119C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587957 | ||||||
chr2:109588094
|
T | C | 28 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(25): Show | 28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-2256A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588094 | ||||||
chr2:109588125
|
C | T | 15 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2287G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588125 | ||||||
chr2:109588336
|
G | C | 1 | a0001c0001t0001g0315 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.100-2498C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588336 | ||||||
chr2:109588533
|
G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-2695C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588533 | ||||||
chr2:109588727
|
G | A | 1 | a0001c0001t0005g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.100-2889C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588727 | ||||||
chr2:109588813
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-2975A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588813 | ||||||
chr2:109588850
|
T | TA | 67 | a0001c0001t0002g0077a0001c0001t0002g0109a0001c0001t0002g0125others(64): Show | 69 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.100-3013dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | ||||||
chr2:109588850
|
T | TAA | 56 | a0001c0001t0001g0321a0001c0001t0002g0145a0001c0001t0003g0001others(53): Show | 60 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.100-3014_100-3013d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | ||||||
chr2:109588850
|
TA | T | 131 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-3013delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | ||||||
chr2:109588870
|
C | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-3032G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588870 | ||||||
chr2:109589102
|
G | T | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3264C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589102 | ||||||
chr2:109589106
|
T | G | 57 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(54): Show | 58 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-3268A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589106 | ||||||
chr2:109589180
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-3342A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589180 | ||||||
chr2:109589258
|
T | C | 60 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.100-3420A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589258 | ||||||
chr2:109589339
|
C | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-3501G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589339 | ||||||
chr2:109589736
|
C | CA | 59 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(56): Show | 60 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.99+3314dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589736 | ||||||
chr2:109589741
|
A | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.99+3310T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589741 | ||||||
chr2:109589825
|
C | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589825 | ||||||
chr2:109589970
|
G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.99+3081C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589970 | ||||||
chr2:109590029
|
CATATATA others(23): Show |
C | 3 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0135 | 3 | HG02647.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+2992_99+3021del others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590029 | ||||||
chr2:109590035
|
T | TAC | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+3014_99+3015dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590035 | ||||||
chr2:109590035
|
TACACACA others(25): Show |
T | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+2984_99+3015del others(32): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590035 | ||||||
chr2:109590041
|
CAT | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0094others(10): Show | 14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+3008_99+3009del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590041 | ||||||
chr2:109590041
|
CATATATA others(27): Show |
C | 5 | a0001c0001t0006g0134a0001c0001t0006g0136a0001c0001t0006g0137others(2): Show | 5 | HG02015.hp2 HG03490.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2976_99+3009del others(34): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590041 | ||||||
chr2:109590048
|
ATGTGTG | A | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2997_99+3002del others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590048 | ||||||
chr2:109590073
|
C | T | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2978G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590073 | ||||||
chr2:109590078
|
A | ATG | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2972_99+2973ins others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590078 | ||||||
chr2:109590078
|
ATATGTAT others(21): Show |
A | 2 | a0001c0001t0001g0253a0001c0001t0002g0076 | 2 | HG00597.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+2945_99+2972del others(28): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590078 | ||||||
chr2:109590108
|
A | ATG | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+2941_99+2942dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590108 | ||||||
chr2:109590129
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99+2922G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590129 | ||||||
chr2:109590392
|
T | C | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+2659A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590392 | ||||||
chr2:109590424
|
CT | C | 65 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(62): Show | 67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+2626delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590424 | ||||||
chr2:109590571
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+2480T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590571 | ||||||
chr2:109590683
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99+2368G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590683 | ||||||
chr2:109590762
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+2289G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590762 | ||||||
chr2:109591046
|
T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0329 | 3 | HG00621.hp2 NA18612.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.99+2005A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591046 | ||||||
chr2:109591085
|
C | T | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+1966G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591085 | ||||||
chr2:109591191
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+1860T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591191 | ||||||
chr2:109591365
|
C | T | 5 | a0001c0001t0004g0193a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 5 | HG01192.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1686G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591365 | ||||||
chr2:109591409
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+1642G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591409 | ||||||
chr2:109591629
|
G | T | 1 | a0001c0001t0002g0215 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.99+1422C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591629 | ||||||
chr2:109591714
|
C | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(232): Show | 244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.99+1337G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591714 | ||||||
chr2:109591734
|
G | A | 235 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(232): Show | 244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.99+1317C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591734 | ||||||
chr2:109591755
|
G | A | 1 | a0001c0001t0004g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.99+1296C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591755 | ||||||
chr2:109591856
|
C | T | 4 | a0001c0001t0007g0337a0001c0001t0007g0342a0001c0001t0007g0343others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1195G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591856 | ||||||
chr2:109591858
|
C | T | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1193G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591858 | ||||||
chr2:109591934
|
T | A | 60 | a0001c0001t0004g0008a0001c0001t0004g0180a0001c0001t0004g0181others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+1117A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591934 | ||||||
chr2:109591975
|
C | A | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1076G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591975 | ||||||
chr2:109592070
|
T | C | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+981A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592070 | ||||||
chr2:109592262
|
C | A | 1 | a0001c0001t0001g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+789G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592262 | ||||||
chr2:109592276
|
G | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+775C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592276 | ||||||
chr2:109592294
|
G | A | 1 | a0001c0001t0001g0370 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.99+757C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592294 | ||||||
chr2:109592395
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.99+656C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592395 | ||||||
chr2:109592419
|
T | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.99+632A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592419 | ||||||
chr2:109592427
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+624G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592427 | ||||||
chr2:109592428
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+623C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592428 | ||||||
chr2:109592629
|
A | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0078 | 3 | HG02615.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+422T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592629 | ||||||
chr2:109592637
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0131 | 2 | HG01255.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.99+414C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592637 | ||||||
chr2:109592705
|
G | C | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99+346C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592705 | ||||||
chr2:109592887
|
A | AT | 11 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(8): Show | 12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+163dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592887 | ||||||
chr2:109593396
|
G | T | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.31-277C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593396 | ||||||
chr2:109593409
|
C | CTTTTTT | 21 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(18): Show | 21 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-296_31-291dupAA others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | ||||||
chr2:109593409
|
C | CTTTTTTT | 33 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(30): Show | 33 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-297_31-291dupAA others(5): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | ||||||
chr2:109593409
|
C | CTTTTTTT others(1): Show |
143 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(140): Show | 151 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.31-298_31-291dupAA others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | ||||||
chr2:109593409
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0139a0001c0001t0002g0162a0001c0001t0003g0022others(3): Show | 6 | HG01192.hp2 HG03225.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-299_31-291dupAA others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | ||||||
chr2:109593409
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-300_31-291dupAA others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | ||||||
chr2:109593474
|
C | T | 146 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(143): Show | 153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.31-355G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593474 | ||||||
chr2:109593847
|
A | T | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31-728T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593847 | ||||||
chr2:109593893
|
C | G | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-774G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593893 | ||||||
chr2:109593894
|
G | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-775C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593894 | ||||||
chr2:109593907
|
T | A | 2 | a0002c0003t0001g0286a0002c0003t0001g0287 | 2 | NA18969.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.31-788A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593907 | ||||||
chr2:109594120
|
T | C | 4 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0103others(1): Show | 5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-1001A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594120 | ||||||
chr2:109594135
|
A | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1016T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594135 | ||||||
chr2:109594149
|
G | A | 14 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(11): Show | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-1030C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594149 | ||||||
chr2:109594271
|
TA | T | 206 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(203): Show | 214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-1153delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594271 | ||||||
chr2:109594285
|
C | T | 15 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-1166G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594285 | ||||||
chr2:109594382
|
C | T | 30 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(27): Show | 30 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-1263G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594382 | ||||||
chr2:109594796
|
T | C | 2 | a0001c0001t0004g0233a0001c0001t0004g0237 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.31-1677A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594796 | ||||||
chr2:109594814
|
T | C | 29 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(26): Show | 30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-1695A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594814 | ||||||
chr2:109594921
|
T | A | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1802A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594921 | ||||||
chr2:109594922
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1803G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594922 | ||||||
chr2:109595012
|
G | A | 128 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(125): Show | 134 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.31-1893C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595012 | ||||||
chr2:109595015
|
C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0093a0001c0001t0005g0094others(10): Show | 14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-1896G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595015 | ||||||
chr2:109595096
|
G | A | 233 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(230): Show | 242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.31-1977C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595096 | ||||||
chr2:109595178
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.31-2059G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595178 | ||||||
chr2:109595280
|
G | A | 3 | a0001c0001t0003g0060a0001c0001t0003g0061a0001c0001t0003g0062 | 3 | HG02135.hp2 NA18984.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.31-2161C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595280 | ||||||
chr2:109595380
|
T | C | 16 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(13): Show | 16 | HG01175.hp1 HG01891.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-2261A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595380 | ||||||
chr2:109595495
|
T | C | 31 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(28): Show | 31 | HG00639.hp1 HG00735.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-2376A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595495 | ||||||
chr2:109595788
|
T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-2669A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595788 | ||||||
chr2:109595877
|
A | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00621.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.31-2758T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595877 | ||||||
chr2:109595966
|
T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-2847A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595966 | ||||||
chr2:109596192
|
C | G | 23 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(20): Show | 23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-3073G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596192 | ||||||
chr2:109596194
|
G | A | 1 | a0004c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.31-3075C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596194 | ||||||
chr2:109596243
|
TTTAATAT others(5): Show |
T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-3136_31-3125del others(12): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596243 | ||||||
chr2:109596333
|
A | C | 60 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(57): Show | 61 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.31-3214T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596333 | ||||||
chr2:109596356
|
G | A | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3237C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596356 | ||||||
chr2:109596474
|
G | A | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.31-3355C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596474 | ||||||
chr2:109596510
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.31-3391C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596510 | ||||||
chr2:109596574
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-3455C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596574 | ||||||
chr2:109596649
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.31-3530G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596649 | ||||||
chr2:109596662
|
T | C | 27 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(24): Show | 27 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-3543A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596662 | ||||||
chr2:109596733
|
T | C | 2 | a0001c0001t0004g0216a0001c0001t0004g0217 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.31-3614A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596733 | ||||||
chr2:109596806
|
G | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0319a0001c0001t0001g0390 | 3 | HG00140.hp2 HG02300.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.31-3687C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596806 | ||||||
chr2:109596822
|
TGA | T | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3705_31-3704del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596822 | ||||||
chr2:109597278
|
A | G | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-4159T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597278 | ||||||
chr2:109597337
|
A | G | 2 | a0001c0001t0005g0094a0001c0001t0005g0102 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.31-4218T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597337 | ||||||
chr2:109597436
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.31-4317C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597436 | ||||||
chr2:109597575
|
TAC | T | 28 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(25): Show | 30 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-4458_31-4457del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597575 | ||||||
chr2:109597805
|
C | A | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.31-4686G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597805 | ||||||
chr2:109597829
|
G | T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4710C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597829 | ||||||
chr2:109597884
|
G | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4765C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597884 | ||||||
chr2:109597885
|
C | T | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-4766G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597885 | ||||||
chr2:109597940
|
C | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0346a0001c0001t0001g0347others(27): Show | 31 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-4821G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597940 | ||||||
chr2:109598067
|
T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-4948A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598067 | ||||||
chr2:109598304
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0261a0001c0001t0001g0278others(2): Show | 5 | HG00544.hp1 NA18939.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-5185C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598304 | ||||||
chr2:109598428
|
A | G | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.31-5309T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598428 | ||||||
chr2:109598528
|
A | C | 1 | a0001c0001t0003g0043 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.31-5409T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598528 | ||||||
chr2:109598532
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.31-5413T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598532 | ||||||
chr2:109598806
|
G | A | 1 | a0001c0001t0001g0390 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31-5687C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598806 | ||||||
chr2:109598812
|
G | A | 1 | a0001c0001t0006g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-5693C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598812 | ||||||
chr2:109598838
|
C | A | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.31-5719G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598838 | ||||||
chr2:109598856
|
G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-5737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598856 | ||||||
chr2:109598901
|
A | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.31-5782T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598901 | ||||||
chr2:109598942
|
T | TG | 4 | a0001c0001t0004g0192a0001c0001t0004g0209a0001c0001t0004g0210others(1): Show | 4 | NA18945.hp2 NA18962.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-5824dupC | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598942 | ||||||
chr2:109599090
|
T | A | 5 | a0001c0001t0001g0340a0001c0001t0007g0337a0001c0001t0007g0342others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-5971A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599090 | ||||||
chr2:109599269
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.31-6150G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599269 | ||||||
chr2:109599448
|
A | G | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG01109.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.31-6329T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599448 | ||||||
chr2:109599458
|
C | CA | 41 | a0001c0001t0001g0322a0001c0001t0001g0330a0001c0001t0001g0332others(38): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.31-6340dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599458 | ||||||
chr2:109599552
|
T | A | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-6433A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599552 | ||||||
chr2:109599590
|
G | C | 3 | a0001c0001t0003g0019a0001c0001t0003g0063a0001c0001t0003g0064 | 3 | NA18947.hp1 NA18971.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.31-6471C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599590 | ||||||
chr2:109599774
|
C | T | 207 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(204): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.31-6655G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599774 | ||||||
chr2:109599963
|
G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-6844C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599963 | ||||||
chr2:109600148
|
A | G | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.31-7029T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600148 | ||||||
chr2:109600190
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-7071A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600190 | ||||||
chr2:109600318
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-7199G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600318 | ||||||
chr2:109600538
|
G | GA | 15 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0336others(12): Show | 15 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-7420dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600538 | ||||||
chr2:109600549
|
A | C | 4 | a0001c0001t0004g0218a0001c0001t0004g0220a0001c0001t0004g0221others(1): Show | 4 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7430T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600549 | ||||||
chr2:109600553
|
C | A | 4 | a0001c0001t0007g0337a0001c0001t0007g0342a0001c0001t0007g0343others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7434G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600553 | ||||||
chr2:109600842
|
C | A | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-7723G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600842 | ||||||
chr2:109600986
|
C | T | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-7867G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600986 | ||||||
chr2:109600995
|
GA | G | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-7877delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600995 | ||||||
chr2:109601049
|
C | T | 29 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(26): Show | 30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-7930G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601049 | ||||||
chr2:109601095
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.31-7976G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601095 | ||||||
chr2:109601178
|
G | C | 1 | a0001c0001t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-8059C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601178 | ||||||
chr2:109601198
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-8079G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601198 | ||||||
chr2:109601273
|
G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-8154C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601273 | ||||||
chr2:109601581
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-8462G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601581 | ||||||
chr2:109601594
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-8475T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601594 | ||||||
chr2:109601757
|
C | A | 5 | a0001c0001t0004g0233a0001c0001t0004g0234a0001c0001t0004g0235others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-8638G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601757 | ||||||
chr2:109601765
|
TA | T | 85 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0002g0166others(82): Show | 90 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.31-8647delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601765 | ||||||
chr2:109601810
|
G | C | 63 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(60): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-8691C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601810 | ||||||
chr2:109601911
|
A | C | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-8792T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601911 | ||||||
chr2:109601956
|
C | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-8837G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601956 | ||||||
chr2:109601961
|
C | T | 1 | a0001c0001t0003g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.31-8842G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601961 | ||||||
chr2:109602201
|
TTA | T | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-9084_31-9083del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602201 | ||||||
chr2:109602306
|
AATTAAG | A | 63 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(60): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-9193_31-9188del others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602306 | ||||||
chr2:109602328
|
T | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.31-9209A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602328 | ||||||
chr2:109602503
|
C | T | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-9384G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602503 | ||||||
chr2:109602636
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.31-9517A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602636 | ||||||
chr2:109602647
|
C | A | 4 | a0001c0001t0002g0112a0001c0001t0002g0128a0001c0001t0002g0129others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9528G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602647 | ||||||
chr2:109602680
|
T | TA | 12 | a0001c0001t0001g0251a0001c0001t0001g0389a0001c0001t0002g0167others(9): Show | 12 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-9562dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602680 | ||||||
chr2:109602680
|
TA | T | 45 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0284others(42): Show | 48 | HG00323.hp2 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.31-9562delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602680 | ||||||
chr2:109602681
|
A | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG00735.hp2 HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.31-9562T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602681 | ||||||
chr2:109602897
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.31-9778C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602897 | ||||||
chr2:109602901
|
C | CA | 84 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(81): Show | 87 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-9783dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | ||||||
chr2:109602901
|
C | CAA | 60 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0003g0001others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-9784_31-9783dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | ||||||
chr2:109602901
|
C | CAAA | 15 | a0001c0001t0003g0065a0001c0001t0005g0005a0001c0001t0005g0092others(12): Show | 16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-9785_31-9783dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | ||||||
chr2:109602901
|
CA | C | 47 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0001t0001g0266others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.31-9783delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | ||||||
chr2:109603039
|
C | CCAG | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(6): Show | 10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-9923_31-9921dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603039 | ||||||
chr2:109603090
|
C | A | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-9971G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603090 | ||||||
chr2:109603091
|
A | C | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-9972T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603091 | ||||||
chr2:109603094
|
A | T | 11 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(8): Show | 12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9975T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603094 | ||||||
chr2:109603246
|
T | A | 16 | a0001c0001t0001g0247a0001c0001t0001g0280a0001c0001t0001g0331others(13): Show | 17 | HG01167.hp1 HG01192.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-10127A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603246 | ||||||
chr2:109603482
|
G | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+10316C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603482 | ||||||
chr2:109603491
|
A | G | 346 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(343): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+10307T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603491 | ||||||
chr2:109603524
|
C | A | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.30+10274G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603524 | ||||||
chr2:109603535
|
G | A | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.30+10263C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603535 | ||||||
chr2:109603542
|
TA | T | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+10255delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603542 | ||||||
chr2:109603758
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+10040A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603758 | ||||||
chr2:109603832
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.30+9966C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603832 | ||||||
chr2:109604110
|
C | T | 11 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(8): Show | 12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+9688G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604110 | ||||||
chr2:109604123
|
C | T | 13 | a0001c0001t0003g0021a0001c0001t0003g0028a0001c0001t0003g0029others(10): Show | 13 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+9675G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604123 | ||||||
chr2:109604139
|
G | A | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+9659C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604139 | ||||||
chr2:109604148
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.30+9650G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604148 | ||||||
chr2:109604161
|
C | CA | 64 | a0001c0001t0001g0250a0001c0001t0001g0333a0001c0001t0001g0347others(61): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+9636dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | ||||||
chr2:109604161
|
C | CAA | 8 | a0001c0001t0002g0077a0001c0001t0004g0196a0001c0001t0004g0233others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+9635_30+9636dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | ||||||
chr2:109604161
|
C | CAAA | 28 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0074others(25): Show | 29 | HG00735.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.30+9634_30+9636dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | ||||||
chr2:109604330
|
G | A | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+9468C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604330 | ||||||
chr2:109604374
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0282 | 2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.30+9424T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604374 | ||||||
chr2:109604383
|
A | AAGGGGAG others(3): Show |
4 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0171others(1): Show | 4 | HG00735.hp1 HG01433.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(3): Show |
126 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(123): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.30+9405_30+9414dup others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(8): Show |
15 | a0001c0001t0002g0213a0001c0001t0005g0005a0001c0001t0005g0092others(12): Show | 16 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(15): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(13): Show |
41 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0004g0008others(38): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(20): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(18): Show |
18 | a0001c0001t0004g0180a0001c0001t0004g0195a0001c0001t0004g0218others(15): Show | 18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(25): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(23): Show |
1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(33): Show |
29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(40): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(28): Show |
99 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(96): Show | 103 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(35): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(29): Show |
1 | a0001c0001t0003g0020 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(36): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(23): Show |
1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604383
|
A | AAGGGGAG others(14): Show |
1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(21): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | ||||||
chr2:109604389
|
A | G | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+9409T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604389 | ||||||
chr2:109604394
|
C | A | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9404G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604394 | ||||||
chr2:109604395
|
G | C | 1 | a0001c0001t0002g0141 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.30+9403C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604395 | ||||||
chr2:109604396
|
G | A | 1 | a0001c0001t0007g0344 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.30+9402C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604396 | ||||||
chr2:109604399
|
C | A | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9399G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604399 | ||||||
chr2:109604406
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9392T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604406 | ||||||
chr2:109604407
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9391T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604407 | ||||||
chr2:109604408
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9390T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604408 | ||||||
chr2:109604410
|
G | GGGGCGGG others(9): Show |
1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9387_30+9388ins others(16): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604410 | ||||||
chr2:109604449
|
G | A | 4 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0072others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9349C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604449 | ||||||
chr2:109604466
|
C | T | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+9332G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604466 | ||||||
chr2:109604482
|
T | A | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+9316A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604482 | ||||||
chr2:109604607
|
G | A | 2 | a0001c0001t0007g0343a0001c0001t0007g0344 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.30+9191C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604607 | ||||||
chr2:109604759
|
G | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0077others(8): Show | 12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+9039C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604759 | ||||||
chr2:109605005
|
A | G | 1 | a0001c0001t0003g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.30+8793T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605005 | ||||||
chr2:109605110
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+8688C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605110 | ||||||
chr2:109605193
|
G | T | 8 | a0001c0001t0006g0016a0001c0001t0006g0133a0001c0001t0006g0134others(5): Show | 8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8605C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605193 | ||||||
chr2:109605289
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.30+8509C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605289 | ||||||
chr2:109605454
|
G | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+8344C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605454 | ||||||
chr2:109605480
|
T | TA | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+8317dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605480 | ||||||
chr2:109605629
|
A | G | 3 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0231 | 3 | HG02109.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.30+8169T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605629 | ||||||
chr2:109605766
|
T | C | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+8032A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605766 | ||||||
chr2:109605976
|
C | A | 1 | a0001c0001t0002g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+7822G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605976 | ||||||
chr2:109606127
|
G | A | 207 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(204): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.30+7671C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606127 | ||||||
chr2:109606139
|
G | A | 1 | a0001c0001t0006g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.30+7659C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606139 | ||||||
chr2:109606232
|
T | C | 8 | a0001c0001t0005g0005a0001c0001t0005g0092a0001c0001t0005g0093others(5): Show | 9 | HG01257.hp1 HG01258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+7566A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606232 | ||||||
chr2:109606282
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+7516C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606282 | ||||||
chr2:109606308
|
C | T | 1 | a0001c0001t0006g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.30+7490G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606308 | ||||||
chr2:109606309
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+7489C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606309 | ||||||
chr2:109606320
|
C | CAGGAGA | 26 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(23): Show | 26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+7472_30+7477dup others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606320 | ||||||
chr2:109606324
|
A | G | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+7474T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606324 | ||||||
chr2:109606339
|
C | T | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+7459G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606339 | ||||||
chr2:109606393
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.30+7405C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606393 | ||||||
chr2:109606440
|
G | T | 1 | a0001c0001t0004g0195 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.30+7358C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606440 | ||||||
chr2:109606582
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.30+7216A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606582 | ||||||
chr2:109606642
|
TA | T | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(334): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.30+7155delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606642 | ||||||
chr2:109606672
|
C | CT | 15 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0340others(12): Show | 15 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+7125dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
C | CTT | 30 | a0001c0001t0002g0204a0001c0001t0002g0213a0001c0001t0004g0008others(27): Show | 31 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+7124_30+7125dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
C | CTTT | 18 | a0001c0001t0002g0190a0001c0001t0004g0180a0001c0001t0004g0181others(15): Show | 18 | HG01109.hp1 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+7123_30+7125dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
C | CTTTT | 14 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0218others(11): Show | 14 | HG00639.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.30+7122_30+7125dup others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
CT | C | 91 | a0001c0001t0001g0381a0001c0001t0001g0382a0001c0001t0002g0017others(88): Show | 95 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.30+7125delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
CTT | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0246a0001c0001t0001g0247others(69): Show | 76 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.30+7124_30+7125del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
CTTT | C | 73 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.30+7123_30+7125del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606672
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0007g0337a0001c0001t0007g0342a0001c0001t0007g0343others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+7116_30+7125del others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | ||||||
chr2:109606714
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.30+7084G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606714 | ||||||
chr2:109606977
|
A | T | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+6821T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606977 | ||||||
chr2:109607074
|
T | G | 1 | a0001c0001t0001g0384 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.30+6724A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607074 | ||||||
chr2:109607234
|
C | T | 208 | a0001c0001t0001g0256a0001c0001t0002g0006a0001c0001t0002g0007others(205): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.30+6564G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607234 | ||||||
chr2:109607246
|
T | C | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+6552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607246 | ||||||
chr2:109607317
|
G | C | 1 | a0001c0001t0001g0012 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.30+6481C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607317 | ||||||
chr2:109607480
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.30+6318C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607480 | ||||||
chr2:109607538
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+6260G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607538 | ||||||
chr2:109607572
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.30+6226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607572 | ||||||
chr2:109607741
|
CCT | C | 4 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0183others(1): Show | 4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+6055_30+6056del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607741 | ||||||
chr2:109608009
|
T | C | 1 | a0001c0001t0001g0336 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.30+5789A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608009 | ||||||
chr2:109608037
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.30+5761A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608037 | ||||||
chr2:109608038
|
T | C | 28 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(25): Show | 28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.30+5760A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608038 | ||||||
chr2:109608066
|
A | ATCTATAC others(3): Show |
2 | a0001c0001t0004g0184a0006c0009t0004g0242 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5731_30+5732ins others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608066 | ||||||
chr2:109608067
|
C | T | 2 | a0001c0001t0004g0184a0006c0009t0004g0242 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5731G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608067 | ||||||
chr2:109608418
|
G | C | 4 | a0001c0001t0007g0337a0001c0001t0007g0342a0001c0001t0007g0343others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+5380C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608418 | ||||||
chr2:109608468
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+5330T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608468 | ||||||
chr2:109608549
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30+5249C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608549 | ||||||
chr2:109608776
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.30+5022T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608776 | ||||||
chr2:109608836
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.30+4962T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608836 | ||||||
chr2:109608863
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+4935G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608863 | ||||||
chr2:109608926
|
C | T | 207 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(204): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.30+4872G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608926 | ||||||
chr2:109609114
|
C | A | 346 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(343): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+4684G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609114 | ||||||
chr2:109609184
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.30+4614T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609184 | ||||||
chr2:109609220
|
T | C | 1 | a0001c0001t0001g0385 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.30+4578A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609220 | ||||||
chr2:109609338
|
GAAT | G | 144 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(141): Show | 151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+4457_30+4459del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609338 | ||||||
chr2:109609358
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0250 | 2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.30+4440G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609358 | ||||||
chr2:109609394
|
T | C | 1 | a0001c0001t0001g0388 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.30+4404A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609394 | ||||||
chr2:109609418
|
G | A | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.30+4380C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609418 | ||||||
chr2:109609501
|
G | T | 63 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(60): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.30+4297C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609501 | ||||||
chr2:109609572
|
C | T | 29 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0132others(26): Show | 31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+4226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609572 | ||||||
chr2:109609611
|
G | A | 40 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(37): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.30+4187C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609611 | ||||||
chr2:109609615
|
CA | C | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.30+4182delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609615 | ||||||
chr2:109609615
|
CAA | C | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG01168.hp2 HG01257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+4181_30+4182del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609615 | ||||||
chr2:109610037
|
C | G | 65 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(62): Show | 67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.30+3761G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610037 | ||||||
chr2:109610095
|
G | GT | 67 | a0001c0001t0001g0345a0001c0001t0002g0006a0001c0001t0002g0007others(64): Show | 69 | HG00597.hp1 HG00609.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.30+3702dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610095
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.30+3693_30+3702dup others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610095
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0004g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.30+3692_30+3702dup others(11): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610095
|
G | GTTTTTTT others(21): Show |
1 | a0001c0001t0004g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+3702_30+3703ins others(28): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610095
|
G | GTTTTTTT others(22): Show |
2 | a0001c0001t0004g0239a0005c0005t0004g0219 | 2 | HG00639.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.30+3702_30+3703ins others(29): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610095
|
G | GTTTTTTT others(38): Show |
1 | a0001c0001t0004g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+3702_30+3703ins others(45): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | ||||||
chr2:109610165
|
T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.30+3633A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610165 | ||||||
chr2:109610192
|
G | A | 64 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(61): Show | 68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+3606C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610192 | ||||||
chr2:109610254
|
A | T | 4 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0183others(1): Show | 4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+3544T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610254 | ||||||
chr2:109610486
|
G | A | 19 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0075others(16): Show | 20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+3312C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610486 | ||||||
chr2:109610490
|
G | A | 5 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+3308C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610490 | ||||||
chr2:109610576
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+3222G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610576 | ||||||
chr2:109610981
|
A | C | 8 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(5): Show | 8 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+2817T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610981 | ||||||
chr2:109610992
|
C | T | 26 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(23): Show | 26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+2806G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610992 | ||||||
chr2:109611000
|
C | T | 1 | a0001c0001t0005g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.30+2798G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611000 | ||||||
chr2:109611067
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2731G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611067 | ||||||
chr2:109611068
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2730T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611068 | ||||||
chr2:109611076
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2722G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611076 | ||||||
chr2:109611078
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2720G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611078 | ||||||
chr2:109611079
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2719T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611079 | ||||||
chr2:109611080
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2718T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611080 | ||||||
chr2:109611082
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2716T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611082 | ||||||
chr2:109611083
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2715T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611083 | ||||||
chr2:109611095
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2703G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611095 | ||||||
chr2:109611096
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2702G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611096 | ||||||
chr2:109611101
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2697G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611101 | ||||||
chr2:109611102
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2696T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611102 | ||||||
chr2:109611104
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2694G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611104 | ||||||
chr2:109611106
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2692T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611106 | ||||||
chr2:109611107
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2691T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611107 | ||||||
chr2:109611108
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2690A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611108 | ||||||
chr2:109611113
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2685G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611113 | ||||||
chr2:109611114
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2684A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611114 | ||||||
chr2:109611117
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2681T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611117 | ||||||
chr2:109611119
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2679G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611119 | ||||||
chr2:109611120
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2678T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611120 | ||||||
chr2:109611121
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2677T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611121 | ||||||
chr2:109611122
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2676G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611122 | ||||||
chr2:109611123
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2675A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611123 | ||||||
chr2:109611126
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2672T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611126 | ||||||
chr2:109611127
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2671G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611127 | ||||||
chr2:109611128
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2670T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611128 | ||||||
chr2:109611130
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2668G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611130 | ||||||
chr2:109611131
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2667G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611131 | ||||||
chr2:109611133
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2665A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611133 | ||||||
chr2:109611134
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2664T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611134 | ||||||
chr2:109611137
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2661G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611137 | ||||||
chr2:109611138
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2660G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611138 | ||||||
chr2:109611139
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2659T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611139 | ||||||
chr2:109611140
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2658T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611140 | ||||||
chr2:109611141
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2657T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611141 | ||||||
chr2:109611142
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2656T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611142 | ||||||
chr2:109611143
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2655T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611143 | ||||||
chr2:109611144
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2654T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611144 | ||||||
chr2:109611145
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2653A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611145 | ||||||
chr2:109611148
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2650G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611148 | ||||||
chr2:109611149
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2649G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611149 | ||||||
chr2:109611150
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2648G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611150 | ||||||
chr2:109611152
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2646G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611152 | ||||||
chr2:109611153
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2645T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611153 | ||||||
chr2:109611154
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2644T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611154 | ||||||
chr2:109611155
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2643G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611155 | ||||||
chr2:109611156
|
T | A | 1 | a0001c0001t0003g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.30+2642A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611156 | ||||||
chr2:109611156
|
T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2642A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611156 | ||||||
chr2:109611314
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2484T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611314 | ||||||
chr2:109611350
|
A | C | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2448T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611350 | ||||||
chr2:109611351
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2447G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611351 | ||||||
chr2:109611357
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2441G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611357 | ||||||
chr2:109611384
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2414T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611384 | ||||||
chr2:109611385
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2413T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611385 | ||||||
chr2:109611386
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2412T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611386 | ||||||
chr2:109611387
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2411T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611387 | ||||||
chr2:109611389
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2409T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611389 | ||||||
chr2:109611391
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2407T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611391 | ||||||
chr2:109611392
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2406T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611392 | ||||||
chr2:109611396
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2402T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611396 | ||||||
chr2:109611397
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2401G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611397 | ||||||
chr2:109611398
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2400T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611398 | ||||||
chr2:109611399
|
G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2399C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611399 | ||||||
chr2:109611401
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2397G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611401 | ||||||
chr2:109611409
|
G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2389C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611409 | ||||||
chr2:109611410
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2388T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611410 | ||||||
chr2:109611412
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2386G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611412 | ||||||
chr2:109611413
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2385T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611413 | ||||||
chr2:109611418
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2380G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611418 | ||||||
chr2:109611424
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2374T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611424 | ||||||
chr2:109611426
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.30+2372T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611426 | ||||||
chr2:109611437
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2361T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611437 | ||||||
chr2:109611459
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2339T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611459 | ||||||
chr2:109611484
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2314T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611484 | ||||||
chr2:109611549
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | NA18968.hp2 NA18995.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.30+2249C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611549 | ||||||
chr2:109611559
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2239T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611559 | ||||||
chr2:109611560
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2238G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611560 | ||||||
chr2:109611561
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2237G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611561 | ||||||
chr2:109611564
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2234G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611564 | ||||||
chr2:109611565
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2233G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611565 | ||||||
chr2:109611567
|
G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2231C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611567 | ||||||
chr2:109611572
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2226T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611572 | ||||||
chr2:109611581
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2217G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611581 | ||||||
chr2:109611583
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2215G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611583 | ||||||
chr2:109611584
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2214G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611584 | ||||||
chr2:109611585
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2213G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611585 | ||||||
chr2:109611589
|
C | A | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2209G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611589 | ||||||
chr2:109611590
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2208G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611590 | ||||||
chr2:109611592
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2206G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611592 | ||||||
chr2:109611596
|
A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2202T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611596 | ||||||
chr2:109611597
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2201T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611597 | ||||||
chr2:109611598
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2200T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611598 | ||||||
chr2:109611601
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2197T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611601 | ||||||
chr2:109611609
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2189T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611609 | ||||||
chr2:109611630
|
C | A | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2168G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611630 | ||||||
chr2:109611632
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2166G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611632 | ||||||
chr2:109611634
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2164G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611634 | ||||||
chr2:109611635
|
C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2163G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611635 | ||||||
chr2:109611637
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2161T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611637 | ||||||
chr2:109611737
|
A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2061T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611737 | ||||||
chr2:109611738
|
G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2060C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611738 | ||||||
chr2:109611739
|
C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2059G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611739 | ||||||
chr2:109611746
|
G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2052C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611746 | ||||||
chr2:109611753
|
C | G | 38 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(35): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.30+2045G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611753 | ||||||
chr2:109611931
|
C | T | 60 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(57): Show | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.30+1867G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611931 | ||||||
chr2:109611991
|
A | G | 346 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(343): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+1807T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611991 | ||||||
chr2:109612014
|
A | G | 10 | a0001c0001t0002g0017a0001c0001t0002g0167a0001c0001t0002g0168others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+1784T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612014 | ||||||
chr2:109612050
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.30+1748A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612050 | ||||||
chr2:109612072
|
G | A | 65 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(62): Show | 67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.30+1726C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612072 | ||||||
chr2:109612238
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+1560T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612238 | ||||||
chr2:109612307
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.30+1491G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612307 | ||||||
chr2:109612679
|
C | A | 80 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0106others(77): Show | 83 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(80): Show |
intron_variant | MODIFIER | c.30+1119G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612679 | ||||||
chr2:109612755
|
G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+1043C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612755 | ||||||
chr2:109612876
|
G | T | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+922C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612876 | ||||||
chr2:109612888
|
A | C | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+910T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612888 | ||||||
chr2:109612916
|
T | C | 23 | a0001c0001t0004g0180a0001c0001t0004g0218a0001c0001t0004g0220others(20): Show | 23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.30+882A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612916 | ||||||
chr2:109612945
|
T | C | 1 | a0001c0001t0004g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.30+853A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612945 | ||||||
chr2:109613021
|
C | A | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+777G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613021 | ||||||
chr2:109613259
|
G | A | 9 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+539C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613259 | ||||||
chr2:109613290
|
G | GA | 8 | a0001c0001t0001g0387a0001c0001t0001g0388a0001c0001t0001g0389others(5): Show | 8 | HG00741.hp2 HG01433.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+507dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613290 | ||||||
chr2:109613294
|
A | C | 1 | a0001c0001t0004g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+504T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613294 | ||||||
chr2:109613318
|
G | A | 64 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(61): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+480C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613318 | ||||||
chr2:109613402
|
G | C | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+396C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613402 | ||||||
chr2:109613517
|
T | C | 1 | a0001c0001t0001g0390 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.30+281A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613517 | ||||||
chr2:109613551
|
C | G | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+247G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613551 | ||||||
chr2:109613670
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+128C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613670 | ||||||
chr2:109613671
|
C | A | 64 | a0001c0001t0002g0190a0001c0001t0002g0204a0001c0001t0002g0213others(61): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+127G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613671 | ||||||
chr2:109613756
|
C | G | 1 | a0001c0001t0003g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.30+42G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613756 |