geneid | 4735 |
---|---|
ensemblid | ENSG00000168385.18 |
hgncid | 7729 |
symbol | SEPTIN2 |
name | septin 2 |
refseq_nuc | NM_004404.5 |
refseq_prot | NP_004395.1 |
ensembl_nuc | ENST00000391971.7 |
ensembl_prot | ENSP00000375832.2 |
mane_status | MANE Select |
chr | chr2 |
start | 241315925 |
end | 241354027 |
strand | + |
ver | v1.2 |
region | chr2:241315925-241354027 |
region5000 | chr2:241310925-241359027 |
regionname0 | SEPTIN2_chr2_241315925_241354027 |
regionname5000 | SEPTIN2_chr2_241310925_241359027 |
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 | 361 | 407 | 86 | 70 | 194 | 13 | 42 | 146 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0002 | 0/0 | 361 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
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 | 1086 | 404 | 86 | 69 | 192 | 13 | 42 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
c0002 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
c0003 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
c0004 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
c0005 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
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 | 0/0 | 2166 | 98 | 7 | 10 | 67 | 4 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0002 | 0/0 | 2166 | 61 | 6 | 10 | 33 | 2 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0003 | 1/0 | 2166 | 49 | 16 | 6 | 16 | 1 | 9 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0004 | 0/0 | 2166 | 42 | 0 | 16 | 22 | 0 | 4 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0005 | 0/0 | 2166 | 34 | 0 | 0 | 32 | 2 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0006 | 0/0 | 2166 | 30 | 11 | 14 | 0 | 3 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0007 | 0/1 | 2166 | 29 | 1 | 6 | 15 | 1 | 5 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0008 | 0/0 | 2166 | 8 | 6 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0009 | 0/0 | 2162 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0010 | 0/0 | 2166 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0011 | 0/0 | 2166 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0012 | 0/0 | 2166 | 5 | 2 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0013 | 0/0 | 2166 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0014 | 0/0 | 2166 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0015 | 0/0 | 2166 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0016 | 0/0 | 2166 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0017 | 0/0 | 2166 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0018 | 0/0 | 2166 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0019 | 0/0 | 2166 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0020 | 0/0 | 2166 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0021 | 0/0 | 2166 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0022 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0023 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0024 | 0/0 | 2166 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0025 | 0/0 | 2166 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0026 | 0/0 | 2166 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0027 | 0/0 | 2166 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0028 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0029 | 0/0 | 2166 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0030 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
t0031 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
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 | 10 | 1 | 2 | 4 | 1 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0005 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0008 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0009 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0010 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0042 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
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 | 1086 | 404 | 86 | 69 | 192 | 13 | 42 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0002 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0004 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0005 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0002c0003 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3251 | 98 | 7 | 10 | 67 | 4 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0002 | 0/0 | 3251 | 59 | 6 | 10 | 32 | 1 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0003 | 1/0 | 3251 | 49 | 16 | 6 | 16 | 1 | 9 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0004 | 0/0 | 3251 | 41 | 0 | 16 | 21 | 0 | 4 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0005 | 0/0 | 3251 | 34 | 0 | 0 | 32 | 2 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0006 | 0/0 | 3251 | 30 | 11 | 14 | 0 | 3 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0007 | 0/1 | 3251 | 29 | 1 | 6 | 15 | 1 | 5 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0008 | 0/0 | 3251 | 7 | 6 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0009 | 0/0 | 3247 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0010 | 0/0 | 3251 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0011 | 0/0 | 3251 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0012 | 0/0 | 3251 | 5 | 2 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0013 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0014 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0015 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0016 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0017 | 0/0 | 3251 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0018 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0019 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0020 | 0/0 | 3251 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0021 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0022 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0023 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0024 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0025 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0026 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0027 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0028 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0029 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0030 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0001t0031 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0002t0008 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0004t0002 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0001c0005t0004 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
a0002c0003t0002 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | copy fasta | chr2 | 241310925 | 241359027 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 1 | 2 | 4 | 1 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0008 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0042 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0005 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0008g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0011g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0012g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0012g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0015g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0015g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0016g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0017g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0017g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0018g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0018g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0020g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0022g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0023g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0024g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0025g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0026g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0027g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0028g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0029g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0030g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0001t0031g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0002t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0004t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0001c0005t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0313 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0059 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00140 | hp1 | a0001 | c0001 | t0029 | g0135 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0312 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0038 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00423 | hp2 | a0001 | c0001 | t0007 | g0035 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00597 | hp1 | a0001 | c0001 | t0009 | g0167 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00597 | hp2 | a0001 | c0001 | t0023 | g0287 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0191 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0303 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00741 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0314 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01071 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0308 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0306 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0174 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01175 | hp2 | a0001 | c0001 | t0026 | g0156 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0315 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0309 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01261 | hp1 | a0001 | c0001 | t0024 | g0193 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0036 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0307 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0036 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0299 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0186 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01934 | hp1 | a0001 | c0001 | t0020 | g0246 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01934 | hp2 | a0001 | c0002 | t0008 | g0149 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0183 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0317 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0175 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02071 | hp2 | a0001 | c0001 | t0020 | g0247 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02080 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0035 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0319 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0178 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0301 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02630 | hp1 | a0001 | c0001 | t0019 | g0276 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02818 | hp1 | a0001 | c0001 | t0019 | g0275 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02818 | hp2 | a0001 | c0001 | t0021 | g0225 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02896 | hp1 | a0001 | c0001 | t0018 | g0302 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02896 | hp2 | a0001 | c0001 | t0017 | g0077 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02897 | hp1 | a0001 | c0001 | t0018 | g0300 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0146 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0147 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0304 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0172 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03130 | hp1 | a0001 | c0001 | t0021 | g0007 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0150 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0151 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0295 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03453 | hp1 | a0001 | c0001 | t0022 | g0243 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03453 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0075 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0188 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03669 | hp2 | a0001 | c0001 | t0027 | g0216 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03710 | hp2 | a0001 | c0001 | t0007 | g0280 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0283 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0182 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0192 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0284 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04184 | hp2 | a0001 | c0001 | t0025 | g0027 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0311 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0288 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0184 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0078 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18943 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18951 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18954 | hp1 | a0001 | c0001 | t0030 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18981 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18984 | hp1 | a0001 | c0005 | t0004 | g0291 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18998 | hp1 | a0001 | c0004 | t0002 | g0259 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19000 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19010 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19010 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19011 | hp1 | a0001 | c0001 | t0031 | g0120 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19012 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19030 | hp1 | a0001 | c0001 | t0028 | g0212 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0200 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19070 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19076 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0296 | EUR | TSI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | GIH | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | GIH | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0297 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0242 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG03471 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG06807 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
NA21309 | hp2 | a0001 | c0001 | t0014 | g0248 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0180 | REF | REF | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0042 | REF | REF | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241346222
|
G | A | 1 | a0002 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.899G>A | p.Arg300His | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/13 | 974/3251 | 899/1086 | 300/361 | chr2 | 241346222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241337694
|
G | A | 1 | a0001c0002 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.498G>A | p.Ala166Ala | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/13 | 573/3251 | 498/1086 | 166/361 | chr2 | 241337694 | ||
chr2:241343814
|
C | T | 1 | a0001c0005 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.759C>T | p.Val253Val | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/13 | 834/3251 | 759/1086 | 253/361 | chr2 | 241343814 | ||
chr2:241350162
|
G | A | 1 | a0001c0004 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1074G>A | p.Gly358Gly | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/13 | 1149/3251 | 1074/1086 | 358/361 | chr2 | 241350162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241315963
|
G | A | 22 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(19): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/13 | 8270 | chr2 | 241315963 | |||||
chr2:241315964
|
T | A | 1 | a0001c0001t0022 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/13 | 8269 | chr2 | 241315964 | |||||
chr2:241352200
|
C | T | 1 | a0001c0001t0026 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2026 | chr2 | 241352200 | |||||
chr2:241352328
|
A | G | 6 | a0001c0001t0001a0001c0001t0012a0001c0001t0025others(3): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*391A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2154 | chr2 | 241352328 | |||||
chr2:241352360
|
C | T | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2186 | chr2 | 241352360 | |||||
chr2:241352507
|
G | A | 1 | a0001c0001t0018 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*570G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2333 | chr2 | 241352507 | |||||
chr2:241352748
|
C | T | 1 | a0001c0001t0011 | 5 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*811C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2574 | chr2 | 241352748 | |||||
chr2:241352892
|
T | C | 1 | a0001c0001t0007 | 29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*955T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2718 | chr2 | 241352892 | |||||
chr2:241352949
|
G | T | 1 | a0001c0001t0021 | 2 | HG02818.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1012G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2775 | chr2 | 241352949 | |||||
chr2:241352963
|
G | T | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(16): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2789 | chr2 | 241352963 | |||||
chr2:241353003
|
C | A | 1 | a0001c0001t0012 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1066C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2829 | chr2 | 241353003 | |||||
chr2:241353101
|
G | C | 1 | a0001c0001t0029 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2927 | chr2 | 241353101 | |||||
chr2:241353153
|
C | T | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0023others(2): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1216C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2979 | chr2 | 241353153 | |||||
chr2:241353229
|
A | G | 1 | a0001c0001t0024 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3055 | chr2 | 241353229 | |||||
chr2:241353355
|
A | C | 1 | a0001c0001t0019 | 2 | HG02630.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1418A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3181 | chr2 | 241353355 | |||||
chr2:241353387
|
A | T | 1 | a0001c0001t0027 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3213 | chr2 | 241353387 | |||||
chr2:241353441
|
A | G | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0023others(3): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1504A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3267 | chr2 | 241353441 | |||||
chr2:241353444
|
C | T | 1 | a0001c0001t0030 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1507C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3270 | chr2 | 241353444 | |||||
chr2:241353529
|
G | C | 3 | a0001c0001t0008a0001c0001t0013a0001c0002t0008 | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1592G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3355 | chr2 | 241353529 | |||||
chr2:241353606
|
A | G | 7 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(4): Show | 111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1669A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3432 | chr2 | 241353606 | |||||
chr2:241353606
|
A | T | 1 | a0001c0001t0016 | 4 | HG01884.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1669A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3432 | chr2 | 241353606 | |||||
chr2:241353754
|
A | T | 1 | a0001c0001t0023 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1817A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3580 | chr2 | 241353754 | |||||
chr2:241353794
|
C | A | 2 | a0001c0001t0005a0001c0001t0020 | 36 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1857C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3620 | chr2 | 241353794 | |||||
chr2:241353816
|
G | A | 1 | a0001c0001t0013 | 4 | HG02922.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1879G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3642 | chr2 | 241353816 | |||||
chr2:241353891
|
AATAG | A | 1 | a0001c0001t0009 | 5 | HG00597.hp1 HG02080.hp1 NA18951.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1958_*1961delGATA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3721 | INFO_REALIGN_3_PRIME | chr2 | 241353891 | ||||
chr2:241353954
|
T | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0017 | 13 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2017T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3780 | chr2 | 241353954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241315997
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+15G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241315997 | ||||||
chr2:241316175
|
G | T | 1 | a0001c0001t0017g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+193G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316175 | ||||||
chr2:241316213
|
C | T | 1 | a0001c0001t0002g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+231C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316213 | ||||||
chr2:241316318
|
C | T | 1 | a0001c0001t0002g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+336C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316318 | ||||||
chr2:241316356
|
G | GCCCGACA others(33): Show |
19 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0054others(16): Show | 21 | HG00099.hp2 HG01123.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+376_-18+415dup others(40): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241316356 | |||||
chr2:241316356
|
G | GCCCGACA others(33): Show |
1 | a0001c0001t0002g0316 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-18+382_-18+383ins others(40): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241316356 | |||||
chr2:241316357
|
C | T | 1 | a0001c0001t0004g0317 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-18+375C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316357 | ||||||
chr2:241316415
|
C | T | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+433C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316415 | ||||||
chr2:241316500
|
G | A | 14 | a0001c0001t0010g0021a0001c0001t0010g0072a0001c0001t0010g0079others(11): Show | 17 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+518G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316500 | ||||||
chr2:241316593
|
A | G | 13 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0001t0004g0284others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+611A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316593 | ||||||
chr2:241316594
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+612G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316594 | ||||||
chr2:241316714
|
G | A | 1 | a0001c0001t0004g0282 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-18+732G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316714 | ||||||
chr2:241316846
|
C | T | 1 | a0001c0001t0004g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-18+864C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316846 | ||||||
chr2:241316942
|
C | G | 1 | a0001c0001t0007g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+960C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316942 | ||||||
chr2:241317136
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+1154C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317136 | ||||||
chr2:241317232
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+1250C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317232 | ||||||
chr2:241317239
|
C | G | 1 | a0001c0001t0001g0278 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-18+1257C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317239 | ||||||
chr2:241317268
|
G | A | 1 | a0001c0001t0004g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+1286G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317268 | ||||||
chr2:241317303
|
T | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-18+1321T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317303 | ||||||
chr2:241317353
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 16 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+1371G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317353 | ||||||
chr2:241317397
|
G | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(71): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-18+1415G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317397 | ||||||
chr2:241317535
|
A | AT | 9 | a0001c0001t0001g0093a0001c0001t0001g0141a0001c0001t0001g0273others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+1570dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241317535 | |||||
chr2:241317578
|
C | G | 1 | a0001c0001t0004g0294 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-18+1596C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317578 | ||||||
chr2:241317749
|
C | T | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1767C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317749 | ||||||
chr2:241317750
|
TTCCGG | T | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1769_-18+1773d others(7): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317750 | ||||||
chr2:241317756
|
G | A | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1774G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317756 | ||||||
chr2:241317880
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-18+1898A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317880 | ||||||
chr2:241317943
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(251): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-18+1961G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317943 | ||||||
chr2:241318121
|
G | GA | 8 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0017others(5): Show | 9 | HG01167.hp1 HG01169.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+2150dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318121 | |||||
chr2:241318136
|
GA | G | 20 | a0001c0001t0002g0048a0001c0001t0002g0067a0001c0001t0002g0068others(17): Show | 24 | HG01123.hp2 HG01261.hp1 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18+2164delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318136 | |||||
chr2:241318147
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | NA18953.hp1 NA19000.hp2 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+2165G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318147 | ||||||
chr2:241318170
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-18+2188G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318170 | ||||||
chr2:241318218
|
T | C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+2236T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318218 | ||||||
chr2:241318420
|
A | G | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-18+2438A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318420 | ||||||
chr2:241318444
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(210): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-18+2462G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318444 | ||||||
chr2:241318702
|
C | CT | 58 | a0001c0001t0001g0092a0001c0001t0001g0136a0001c0001t0002g0066others(55): Show | 66 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-18+2737dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318702 | |||||
chr2:241318702
|
CT | C | 11 | a0001c0001t0001g0095a0001c0001t0003g0197a0001c0001t0005g0196others(8): Show | 13 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+2737delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318702 | |||||
chr2:241318853
|
A | G | 1 | a0001c0001t0007g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+2871A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318853 | ||||||
chr2:241319232
|
G | C | 1 | a0001c0001t0011g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18+3250G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319232 | ||||||
chr2:241319307
|
A | G | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+3325A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319307 | ||||||
chr2:241319529
|
A | G | 2 | a0001c0001t0004g0171a0001c0001t0004g0285 | 2 | HG01192.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-18+3547A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319529 | ||||||
chr2:241319547
|
T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+3565T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319547 | ||||||
chr2:241319557
|
G | A | 1 | a0001c0001t0007g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-18+3575G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319557 | ||||||
chr2:241319596
|
C | T | 1 | a0001c0001t0007g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+3614C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319596 | ||||||
chr2:241319737
|
G | A | 2 | a0001c0001t0004g0142a0001c0001t0004g0145 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-18+3755G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319737 | ||||||
chr2:241319792
|
C | G | 69 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(66): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-18+3810C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319792 | ||||||
chr2:241319820
|
C | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+3838C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319820 | ||||||
chr2:241320035
|
C | CT | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 106 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-18+4054dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241320035 | |||||
chr2:241320114
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0020g0246a0001c0001t0020g0247 | 5 | HG01934.hp1 HG02071.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-4102C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320114 | ||||||
chr2:241320199
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(249): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.-17-4017G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320199 | ||||||
chr2:241320512
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-3704G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320512 | ||||||
chr2:241320521
|
C | T | 1 | a0001c0001t0011g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-3695C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320521 | ||||||
chr2:241320578
|
G | C | 1 | a0001c0001t0006g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-17-3638G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320578 | ||||||
chr2:241320724
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0277 | 2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-17-3492G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320724 | ||||||
chr2:241320783
|
C | T | 1 | a0001c0001t0005g0015 | 3 | NA18946.hp2 NA19054.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-17-3433C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320783 | ||||||
chr2:241320925
|
G | C | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-17-3291G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320925 | ||||||
chr2:241321030
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-3186A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321030 | ||||||
chr2:241321065
|
T | G | 9 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0146others(6): Show | 11 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-3151T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321065 | ||||||
chr2:241321107
|
A | C | 1 | a0001c0001t0007g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-3109A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321107 | ||||||
chr2:241321149
|
A | G | 1 | a0001c0001t0002g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-3067A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321149 | ||||||
chr2:241321247
|
A | G | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-2969A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321247 | ||||||
chr2:241321282
|
T | G | 5 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(2): Show | 6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2934T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321282 | ||||||
chr2:241321341
|
G | C | 69 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(66): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-17-2875G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321341 | ||||||
chr2:241321516
|
C | G | 5 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(2): Show | 6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2700C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321516 | ||||||
chr2:241321573
|
G | GT | 8 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0002g0056others(5): Show | 8 | HG00438.hp1 HG00621.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-2633dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241321573 | |||||
chr2:241321596
|
C | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-17-2620C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321596 | ||||||
chr2:241321663
|
T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17-2553T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321663 | ||||||
chr2:241321742
|
C | G | 1 | a0001c0001t0005g0245 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-2474C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321742 | ||||||
chr2:241321748
|
T | G | 1 | a0001c0001t0006g0297 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-2468T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321748 | ||||||
chr2:241321825
|
T | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-17-2391T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321825 | ||||||
chr2:241322019
|
A | G | 15 | a0001c0001t0002g0016a0001c0001t0006g0296a0001c0001t0006g0303others(12): Show | 17 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-2197A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322019 | ||||||
chr2:241322090
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-2126A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322090 | ||||||
chr2:241322099
|
C | G | 1 | a0001c0001t0003g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-2117C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322099 | ||||||
chr2:241322167
|
T | C | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-2049T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322167 | ||||||
chr2:241322387
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(212): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-17-1829T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322387 | ||||||
chr2:241322449
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(71): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-1767A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322449 | ||||||
chr2:241322464
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(75): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-17-1752G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322464 | ||||||
chr2:241322480
|
G | A | 1 | a0001c0001t0007g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-17-1736G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322480 | ||||||
chr2:241322484
|
G | C | 1 | a0001c0001t0003g0199 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-1732G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322484 | ||||||
chr2:241322499
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0265 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-17-1717C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322499 | ||||||
chr2:241322500
|
G | C | 1 | a0001c0001t0019g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-1716G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322500 | ||||||
chr2:241322526
|
G | T | 51 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(48): Show | 58 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-17-1690G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322526 | ||||||
chr2:241322603
|
C | T | 1 | a0001c0001t0007g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-17-1613C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322603 | ||||||
chr2:241322664
|
AT | A | 4 | a0001c0001t0002g0048a0001c0001t0002g0270a0001c0001t0002g0271others(1): Show | 5 | NA18939.hp1 NA18954.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-1547delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241322664 | |||||
chr2:241322700
|
C | G | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-1516C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322700 | ||||||
chr2:241322720
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-17-1496C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322720 | ||||||
chr2:241322896
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(75): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-17-1320A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322896 | ||||||
chr2:241322940
|
C | T | 2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-1276C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322940 | ||||||
chr2:241322991
|
C | CAT | 30 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(27): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-17-1215_-17-1214d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241322991 | |||||
chr2:241323049
|
T | C | 1 | a0001c0001t0024g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-1167T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323049 | ||||||
chr2:241323124
|
C | T | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(3): Show | 6 | NA18949.hp1 NA18951.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1092C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323124 | ||||||
chr2:241323148
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-17-1068C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323148 | ||||||
chr2:241323160
|
C | T | 1 | a0001c0001t0010g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-17-1056C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323160 | ||||||
chr2:241323172
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-17-1044T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323172 | ||||||
chr2:241323174
|
A | ATT | 7 | a0001c0001t0006g0296a0001c0001t0006g0309a0001c0001t0006g0310others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-1027_-17-1026d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241323174 | |||||
chr2:241323174
|
AT | A | 13 | a0001c0001t0001g0096a0001c0001t0002g0270a0001c0001t0004g0154others(10): Show | 14 | HG01261.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-1026delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241323174 | |||||
chr2:241323298
|
G | A | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-918G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323298 | ||||||
chr2:241323408
|
G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-808G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323408 | ||||||
chr2:241323571
|
G | A | 25 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(22): Show | 31 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-645G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323571 | ||||||
chr2:241323596
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17-620C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323596 | ||||||
chr2:241323808
|
G | A | 23 | a0001c0001t0007g0004a0001c0001t0007g0035a0001c0001t0007g0036others(20): Show | 29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-408G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323808 | ||||||
chr2:241323857
|
A | G | 1 | a0001c0001t0007g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-17-359A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323857 | ||||||
chr2:241324021
|
C | T | 5 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(2): Show | 6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-195C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324021 | ||||||
chr2:241324039
|
T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0250a0001c0001t0002g0251 | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-177T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324039 | ||||||
chr2:241324138
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-78C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324138 | ||||||
chr2:241324173
|
T | C | 2 | a0001c0001t0004g0283a0001c0001t0004g0286 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-17-43T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324173 | ||||||
chr2:241324200
|
G | T | 1 | a0001c0001t0007g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-16G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324200 | ||||||
chr2:241324342
|
A | G | 6 | a0001c0001t0003g0043a0001c0001t0003g0237a0001c0001t0003g0238others(3): Show | 7 | HG00544.hp2 HG02129.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+101A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324342 | ||||||
chr2:241324381
|
T | C | 1 | a0001c0001t0010g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9+140T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324381 | ||||||
chr2:241324388
|
CT | C | 31 | a0001c0001t0001g0027a0001c0001t0001g0130a0001c0001t0001g0136others(28): Show | 45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.9+164delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | |||||
chr2:241324388
|
CTT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(236): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.9+163_9+164delTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | |||||
chr2:241324388
|
CTTT | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0273a0001c0001t0002g0054others(7): Show | 11 | HG01167.hp1 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+162_9+164delTTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | |||||
chr2:241324652
|
T | C | 1 | a0001c0001t0010g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9+411T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324652 | ||||||
chr2:241324776
|
CTTAG | C | 6 | a0001c0001t0003g0043a0001c0001t0003g0237a0001c0001t0003g0238others(3): Show | 7 | HG00544.hp2 HG02129.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+538_9+541delAGTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324776 | |||||
chr2:241324834
|
A | C | 13 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0001t0004g0284others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+593A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324834 | ||||||
chr2:241324856
|
A | G | 1 | a0001c0001t0004g0284 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9+615A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324856 | ||||||
chr2:241324968
|
G | GT | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(184): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.9+737dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324968 | |||||
chr2:241325075
|
C | CA | 43 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0016others(40): Show | 52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.9+844dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241325075 | |||||
chr2:241325211
|
G | A | 48 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(45): Show | 54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.10-782G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325211 | ||||||
chr2:241325428
|
A | G | 1 | a0001c0001t0002g0269 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.10-565A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325428 | ||||||
chr2:241325500
|
G | C | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | NA18939.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.10-493G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325500 | ||||||
chr2:241325709
|
C | T | 1 | a0001c0001t0005g0014 | 3 | HG02074.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.10-284C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325709 | ||||||
chr2:241325718
|
A | G | 1 | a0001c0001t0004g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.10-275A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325718 | ||||||
chr2:241325777
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.10-216A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325777 | ||||||
chr2:241325858
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(212): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.10-135C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325858 | ||||||
chr2:241325898
|
C | A | 63 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(60): Show | 72 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.10-95C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325898 | ||||||
chr2:241326248
|
A | G | 4 | a0001c0001t0002g0048a0001c0001t0002g0270a0001c0001t0002g0271others(1): Show | 5 | NA18939.hp1 NA18954.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+135A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326248 | ||||||
chr2:241326249
|
T | C | 1 | a0001c0001t0002g0056 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.130+136T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326249 | ||||||
chr2:241326334
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0086others(9): Show | 17 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+221T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326334 | ||||||
chr2:241326400
|
TCCCTTCC others(142): Show |
T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(251): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.130+438_130+586del | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241326400 | |||||
chr2:241326648
|
A | G | 1 | a0001c0001t0013g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130+535A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326648 | ||||||
chr2:241326664
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(75): Show | 107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.130+551C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326664 | ||||||
chr2:241326925
|
C | G | 9 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0146others(6): Show | 11 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+812C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326925 | ||||||
chr2:241326947
|
A | G | 1 | a0001c0005t0004g0291 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.130+834A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326947 | ||||||
chr2:241327002
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+889C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327002 | ||||||
chr2:241327050
|
CA | C | 46 | a0001c0001t0001g0022a0001c0001t0001g0087a0001c0001t0001g0088others(43): Show | 58 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.130+965delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | |||||
chr2:241327050
|
CAA | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(124): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.130+964_130+965del others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | |||||
chr2:241327050
|
CAAA | C | 102 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0125others(99): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.130+963_130+965del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | |||||
chr2:241327050
|
CAAAA | C | 27 | a0001c0001t0001g0274a0001c0001t0002g0064a0001c0001t0002g0264others(24): Show | 33 | HG00423.hp2 HG00544.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.130+962_130+965del others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | |||||
chr2:241327084
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.130+971G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327084 | ||||||
chr2:241327105
|
C | T | 1 | a0001c0001t0006g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+992C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327105 | ||||||
chr2:241327161
|
T | C | 1 | a0001c0001t0007g0180 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.130+1048T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327161 | ||||||
chr2:241327371
|
G | A | 3 | a0001c0001t0007g0181a0001c0001t0007g0182a0001c0001t0007g0191 | 3 | HG00639.hp2 HG03927.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.130+1258G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327371 | ||||||
chr2:241327508
|
C | CA | 47 | a0001c0001t0001g0101a0001c0001t0002g0044a0001c0001t0002g0250others(44): Show | 58 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130+1407dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327508 | |||||
chr2:241327508
|
C | CAA | 48 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0045others(45): Show | 54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.130+1406_130+1407d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327508 | |||||
chr2:241327548
|
G | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(316): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.130+1435G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327548 | ||||||
chr2:241327820
|
A | G | 2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+1707A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327820 | ||||||
chr2:241327823
|
G | C | 1 | a0001c0001t0006g0298 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130+1710G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327823 | ||||||
chr2:241327898
|
T | C | 1 | a0001c0001t0003g0237 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.130+1785T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327898 | ||||||
chr2:241328018
|
G | A | 1 | a0001c0001t0008g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+1905G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328018 | ||||||
chr2:241328099
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.130+1986G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328099 | ||||||
chr2:241328202
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(279): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.130+2089G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328202 | ||||||
chr2:241328219
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.130+2106G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328219 | ||||||
chr2:241328277
|
A | C | 1 | a0001c0001t0003g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+2164A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328277 | ||||||
chr2:241328401
|
T | G | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130+2288T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328401 | ||||||
chr2:241328483
|
T | TCACAGCA others(10): Show |
2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+2372_130+2388d others(19): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241328483 | |||||
chr2:241328586
|
T | C | 7 | a0001c0001t0003g0043a0001c0001t0003g0219a0001c0001t0003g0237others(4): Show | 8 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+2473T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328586 | ||||||
chr2:241328657
|
A | C | 1 | a0001c0001t0004g0284 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.130+2544A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328657 | ||||||
chr2:241328785
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130+2672G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328785 | ||||||
chr2:241328849
|
C | T | 68 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(65): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.130+2736C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328849 | ||||||
chr2:241328862
|
A | G | 10 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0053others(7): Show | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+2749A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328862 | ||||||
chr2:241328866
|
C | CA | 1 | a0001c0001t0001g0010 | 3 | HG03491.hp1 HG03492.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130+2757dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241328866 | |||||
chr2:241328944
|
C | T | 4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+2831C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328944 | ||||||
chr2:241328960
|
C | T | 2 | a0001c0001t0003g0229a0001c0001t0003g0230 | 2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.130+2847C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328960 | ||||||
chr2:241328976
|
C | T | 4 | a0001c0001t0002g0047a0001c0001t0002g0252a0001c0001t0002g0258others(1): Show | 5 | HG02132.hp2 NA18994.hp2 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+2863C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328976 | ||||||
chr2:241329007
|
T | A | 18 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0048others(15): Show | 21 | HG00609.hp1 HG01106.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+2894T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329007 | ||||||
chr2:241329021
|
T | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(147): Show | 192 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.130+2908T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329021 | ||||||
chr2:241329095
|
TTTG | T | 4 | a0001c0001t0002g0063a0001c0001t0003g0215a0001c0001t0006g0313others(1): Show | 4 | HG00099.hp1 HG01069.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+2997_130+2999d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241329095 | |||||
chr2:241329321
|
G | T | 53 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.130+3208G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329321 | ||||||
chr2:241329339
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.130+3226A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329339 | ||||||
chr2:241329363
|
C | G | 1 | a0001c0005t0004g0291 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.130+3250C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329363 | ||||||
chr2:241329413
|
TACAC | T | 4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+3302_130+3305d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241329413 | |||||
chr2:241329415
|
C | A | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18982.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.130+3302C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329415 | ||||||
chr2:241329416
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.130+3303A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329416 | ||||||
chr2:241329579
|
T | C | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.130+3466T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329579 | ||||||
chr2:241329581
|
C | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130+3468C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329581 | ||||||
chr2:241329593
|
C | T | 42 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(39): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+3480C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329593 | ||||||
chr2:241329609
|
A | G | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.130+3496A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329609 | ||||||
chr2:241329719
|
G | C | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+3606G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329719 | ||||||
chr2:241329888
|
T | A | 72 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(69): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.130+3775T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329888 | ||||||
chr2:241329939
|
C | T | 1 | a0001c0001t0006g0037 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.130+3826C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329939 | ||||||
chr2:241330060
|
C | T | 7 | a0001c0001t0005g0006a0001c0001t0005g0040a0001c0001t0005g0201others(4): Show | 11 | HG00423.hp1 HG02056.hp1 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+3947C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330060 | ||||||
chr2:241330086
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130+3973C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330086 | ||||||
chr2:241330224
|
A | G | 5 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(2): Show | 6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+4111A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330224 | ||||||
chr2:241330373
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.130+4260C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330373 | ||||||
chr2:241330941
|
T | G | 1 | a0001c0001t0005g0208 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.131-4185T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330941 | ||||||
chr2:241330981
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-4145C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330981 | ||||||
chr2:241331018
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(71): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.131-4108A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331018 | ||||||
chr2:241331085
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.131-4041G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331085 | ||||||
chr2:241331175
|
T | A | 1 | a0001c0001t0002g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.131-3951T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331175 | ||||||
chr2:241331657
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-3469C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331657 | ||||||
chr2:241331844
|
G | A | 1 | a0001c0001t0005g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.131-3282G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331844 | ||||||
chr2:241331920
|
A | C | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.131-3206A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331920 | ||||||
chr2:241332129
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.131-2997T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332129 | ||||||
chr2:241332151
|
TTTC | T | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-2972_131-2970d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241332151 | |||||
chr2:241332212
|
T | G | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.131-2914T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332212 | ||||||
chr2:241332275
|
A | G | 5 | a0001c0001t0003g0203a0001c0001t0003g0226a0001c0001t0003g0227others(2): Show | 5 | HG00558.hp1 NA18941.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2851A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332275 | ||||||
chr2:241332652
|
A | G | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.131-2474A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332652 | ||||||
chr2:241332709
|
A | T | 4 | a0001c0001t0013g0147a0001c0001t0013g0150a0001c0001t0013g0151others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-2417A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332709 | ||||||
chr2:241332751
|
TG | T | 13 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0001t0004g0284others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-2374delG | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332751 | ||||||
chr2:241332952
|
G | A | 1 | a0001c0001t0013g0150 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.131-2174G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332952 | ||||||
chr2:241332973
|
A | G | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-2153A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332973 | ||||||
chr2:241333071
|
A | G | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-2055A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333071 | ||||||
chr2:241333073
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.131-2053A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333073 | ||||||
chr2:241333107
|
G | A | 1 | a0001c0001t0007g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-2019G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333107 | ||||||
chr2:241333200
|
A | G | 51 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(48): Show | 58 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.131-1926A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333200 | ||||||
chr2:241333226
|
A | C | 1 | a0001c0001t0002g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.131-1900A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333226 | ||||||
chr2:241333307
|
T | C | 13 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0001t0004g0284others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-1819T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333307 | ||||||
chr2:241333351
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-1775G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333351 | ||||||
chr2:241333407
|
C | G | 1 | a0001c0001t0006g0304 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.131-1719C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333407 | ||||||
chr2:241333480
|
C | G | 1 | a0001c0001t0005g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.131-1646C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333480 | ||||||
chr2:241333578
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0029g0135 | 3 | HG00140.hp1 HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.131-1548C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333578 | ||||||
chr2:241333621
|
T | TGCCTCA | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(149): Show | 194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.131-1500_131-1499i others(8): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241333621 | |||||
chr2:241333648
|
C | T | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1478C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333648 | ||||||
chr2:241333649
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.131-1477G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333649 | ||||||
chr2:241333661
|
G | A | 3 | a0001c0001t0003g0226a0001c0001t0003g0227a0001c0001t0003g0236 | 3 | NA19006.hp1 NA19065.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.131-1465G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333661 | ||||||
chr2:241333664
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.131-1462C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333664 | ||||||
chr2:241333743
|
T | A | 1 | a0001c0001t0004g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.131-1383T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333743 | ||||||
chr2:241333799
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0014g0172 | 2 | HG03098.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.131-1327G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333799 | ||||||
chr2:241333931
|
ATCTCTAA others(9): Show |
A | 1 | a0001c0001t0006g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.131-1192_131-1177d others(18): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241333931 | |||||
chr2:241333979
|
T | C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.131-1147T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333979 | ||||||
chr2:241334027
|
G | GT | 25 | a0001c0001t0001g0123a0001c0001t0006g0189a0001c0001t0007g0004others(22): Show | 31 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.131-1091dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241334027 | |||||
chr2:241334143
|
G | A | 2 | a0001c0001t0003g0211a0001c0001t0003g0221 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.131-983G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334143 | ||||||
chr2:241334169
|
C | G | 1 | a0001c0001t0003g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.131-957C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334169 | ||||||
chr2:241334204
|
C | A | 3 | a0001c0001t0002g0044a0001c0001t0002g0250a0001c0001t0002g0251 | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-922C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334204 | ||||||
chr2:241334218
|
T | A | 2 | a0001c0001t0010g0021a0001c0001t0010g0079 | 3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.131-908T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334218 | ||||||
chr2:241334412
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-714A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334412 | ||||||
chr2:241334456
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.131-670C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334456 | ||||||
chr2:241334497
|
T | A | 2 | a0001c0001t0017g0077a0001c0001t0017g0319 | 2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.131-629T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334497 | ||||||
chr2:241334725
|
C | A | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-401C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334725 | ||||||
chr2:241334727
|
G | A | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-399G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334727 | ||||||
chr2:241334738
|
A | G | 1 | a0001c0001t0007g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-388A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334738 | ||||||
chr2:241334895
|
C | G | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-231C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334895 | ||||||
chr2:241335074
|
G | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.131-52G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241335074 | ||||||
chr2:241335356
|
G | A | 2 | a0001c0001t0010g0021a0001c0001t0010g0079 | 3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.217+144G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335356 | ||||||
chr2:241335367
|
C | T | 4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+155C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335367 | ||||||
chr2:241335406
|
G | A | 2 | a0001c0001t0004g0158a0001c0001t0004g0160 | 2 | NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.217+194G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335406 | ||||||
chr2:241335577
|
C | T | 1 | a0001c0001t0006g0308 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.217+365C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335577 | ||||||
chr2:241335583
|
C | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(71): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.217+371C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335583 | ||||||
chr2:241335652
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218-323C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335652 | ||||||
chr2:241335653
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218-322T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335653 | ||||||
chr2:241335847
|
C | A | 20 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0142others(17): Show | 25 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.218-128C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335847 | ||||||
chr2:241336136
|
C | G | 14 | a0001c0001t0010g0021a0001c0001t0010g0072a0001c0001t0010g0079others(11): Show | 17 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.341+38C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336136 | ||||||
chr2:241336164
|
G | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.341+66G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336164 | ||||||
chr2:241336376
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0250 | 3 | HG00642.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.341+278G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336376 | ||||||
chr2:241336529
|
C | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.341+431C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336529 | ||||||
chr2:241336746
|
A | G | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.342-636A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336746 | ||||||
chr2:241336747
|
T | C | 1 | a0001c0001t0007g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.342-635T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336747 | ||||||
chr2:241336748
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0134 | 2 | HG00438.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.342-634G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336748 | ||||||
chr2:241336829
|
C | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.342-553C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336829 | ||||||
chr2:241336834
|
G | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.342-548G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336834 | ||||||
chr2:241336957
|
G | A | 1 | a0001c0001t0006g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.342-425G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336957 | ||||||
chr2:241337026
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(151): Show | 197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.342-356A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337026 | ||||||
chr2:241337051
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.342-331G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337051 | ||||||
chr2:241337060
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.342-322C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337060 | ||||||
chr2:241337093
|
C | CA | 30 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(27): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-278dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 241337093 | |||||
chr2:241337093
|
CA | C | 25 | a0001c0001t0002g0251a0001c0001t0006g0189a0001c0001t0007g0004others(22): Show | 31 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.342-278delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 241337093 | |||||
chr2:241337108
|
C | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.342-274C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337108 | ||||||
chr2:241337614
|
A | G | 10 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0053others(7): Show | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.477-59A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 6/12 | chr2 | 241337614 | ||||||
chr2:241338029
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+239C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338029 | ||||||
chr2:241338246
|
G | A | 1 | a0001c0001t0004g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.594+456G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338246 | ||||||
chr2:241338300
|
G | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+510G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338300 | ||||||
chr2:241338402
|
C | T | 1 | a0001c0001t0029g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.594+612C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338402 | ||||||
chr2:241338417
|
C | T | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+627C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338417 | ||||||
chr2:241338418
|
C | T | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+628C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338418 | ||||||
chr2:241338459
|
G | T | 1 | a0001c0001t0009g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.594+669G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338459 | ||||||
chr2:241338590
|
AAT | A | 42 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(39): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+813_594+814del others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338590 | |||||
chr2:241338592
|
T | A | 25 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(22): Show | 31 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.594+802T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338592 | ||||||
chr2:241338594
|
T | A | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+804T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338594 | ||||||
chr2:241338597
|
A | G | 1 | a0001c0001t0005g0245 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.594+807A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338597 | ||||||
chr2:241338603
|
A | T | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+813A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338603 | ||||||
chr2:241338624
|
A | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | NA18992.hp2 NA18998.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+834A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338624 | ||||||
chr2:241338649
|
T | C | 4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+859T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338649 | ||||||
chr2:241338668
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.594+878T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338668 | ||||||
chr2:241338687
|
G | A | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+897G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338687 | ||||||
chr2:241338702
|
T | TTTATATT others(23): Show |
1 | a0001c0001t0001g0026 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.594+928_594+957dup others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338702 | |||||
chr2:241338713
|
TATATA | T | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+929_594+933del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338713 | |||||
chr2:241338719
|
ATATAT | A | 21 | a0001c0001t0003g0043a0001c0001t0003g0219a0001c0001t0003g0237others(18): Show | 22 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.594+935_594+939del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338719 | |||||
chr2:241338721
|
ATAT | A | 29 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(26): Show | 35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.594+935_594+937del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338721 | |||||
chr2:241338728
|
A | G | 1 | a0001c0001t0009g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.594+938A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338728 | ||||||
chr2:241338767
|
T | TATATATA others(24): Show |
1 | a0001c0001t0016g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.594+981_594+1011du others(32): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338767 | |||||
chr2:241338767
|
T | TATATATA others(110): Show |
2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.594+1011_594+1012i others(119): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338767 | |||||
chr2:241338771
|
T | TATATATA others(23): Show |
1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.594+985_594+986ins others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TATATATT others(21): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0087others(5): Show | 13 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.594+985_594+986ins others(28): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TATATTAT others(20): Show |
2 | a0001c0001t0016g0049a0001c0001t0016g0299 | 3 | HG01884.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.594+999_594+1000in others(28): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TATATTAT others(24): Show |
91 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.594+1012_594+1042d others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TATATTTA others(19): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0090 | 2 | NA18955.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.594+986_594+987ins others(26): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TATTATAT others(22): Show |
1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.594+983_594+984ins others(29): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | |||||
chr2:241338771
|
T | TTATATTT others(20): Show |
1 | a0001c0001t0001g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.594+981_594+982ins others(27): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338771 | ||||||
chr2:241338772
|
ATATT | A | 2 | a0001c0001t0010g0021a0001c0001t0010g0079 | 3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+983_594+986del others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338772 | ||||||
chr2:241338802
|
C | CATATATT others(52): Show |
42 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(39): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+1016_594+1017i others(61): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | |||||
chr2:241338802
|
C | CATATATT others(83): Show |
1 | a0001c0001t0004g0166 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.594+1016_594+1017i others(92): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | |||||
chr2:241338802
|
C | CATATTAT others(24): Show |
76 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(73): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.594+1017_594+1047d others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | |||||
chr2:241338802
|
C | T | 5 | a0001c0001t0016g0049a0001c0001t0016g0299a0001c0001t0016g0301others(2): Show | 6 | HG01884.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1012C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338802 | ||||||
chr2:241338806
|
T | TTATATTT others(21): Show |
1 | a0001c0001t0001g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.594+1042_594+1043i others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338806 | |||||
chr2:241338820
|
T | TTTATATA others(20): Show |
4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1047_594+1048i others(29): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338820 | |||||
chr2:241338821
|
TTATATAT others(76): Show |
T | 8 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0146others(5): Show | 10 | HG01496.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+1038_594+1120d others(85): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338821 | |||||
chr2:241338830
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+1047_594+1048i others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338830 | |||||
chr2:241338838
|
A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1048A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338838 | ||||||
chr2:241338840
|
T | TATTTATA others(13): Show |
1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1051_594+1052i others(22): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338840 | |||||
chr2:241338842
|
A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1052A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338842 | ||||||
chr2:241338853
|
T | C | 1 | a0002c0003t0002g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.594+1063T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338853 | ||||||
chr2:241338854
|
A | G | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1064A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338854 | ||||||
chr2:241338857
|
TAA | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0258 | 3 | NA19075.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.594+1071_594+1072d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338857 | |||||
chr2:241338859
|
A | T | 2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.594+1069A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338859 | ||||||
chr2:241338861
|
AAT | A | 5 | a0001c0001t0001g0088a0001c0001t0006g0037a0001c0001t0006g0194others(2): Show | 6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1080_594+1081d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338861 | |||||
chr2:241338866
|
A | AT | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+1077dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338866 | |||||
chr2:241338881
|
C | CTATAATA others(118): Show |
1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.594+1128_594+1129i others(127): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338881 | |||||
chr2:241338889
|
T | C | 1 | a0001c0001t0005g0205 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.594+1099T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338889 | ||||||
chr2:241338890
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.594+1100A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338890 | ||||||
chr2:241338910
|
AAT | A | 30 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0016others(27): Show | 36 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.594+1128_594+1129d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338910 | |||||
chr2:241338921
|
TTG | T | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+1133_594+1134d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338921 | |||||
chr2:241338944
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.594+1154A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338944 | ||||||
chr2:241338945
|
TTA | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0006g0295others(2): Show | 5 | HG02257.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+1164_594+1165d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338945 | |||||
chr2:241338951
|
A | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.594+1161A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338951 | ||||||
chr2:241338954
|
T | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+1164T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338954 | ||||||
chr2:241338955
|
A | T | 26 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(23): Show | 32 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.594+1165A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338955 | ||||||
chr2:241338961
|
TA | T | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+1172delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338961 | ||||||
chr2:241338962
|
A | ATTATAAA others(18): Show |
1 | a0001c0001t0027g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.594+1184_594+1208d others(27): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338962 | |||||
chr2:241338967
|
AAATAT | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+1184_594+1188d others(7): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338967 | |||||
chr2:241338971
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+1181A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338971 | ||||||
chr2:241338984
|
ATATT | A | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1198_594+1201d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338984 | |||||
chr2:241338991
|
TA | T | 6 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(3): Show | 7 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1204delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338991 | |||||
chr2:241338992
|
AAAT | A | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+1204_594+1206d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338992 | |||||
chr2:241339034
|
ATAT | A | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.594+1248_594+1250d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339034 | |||||
chr2:241339132
|
G | A | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+1342G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339132 | ||||||
chr2:241339144
|
T | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(279): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.594+1354T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339144 | ||||||
chr2:241339156
|
G | C | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.594+1366G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339156 | ||||||
chr2:241339192
|
G | A | 1 | a0001c0001t0007g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.594+1402G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339192 | ||||||
chr2:241339264
|
G | T | 10 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0053others(7): Show | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.594+1474G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339264 | ||||||
chr2:241339291
|
G | C | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.594+1501G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339291 | ||||||
chr2:241339357
|
A | AG | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+1568dupG | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339357 | |||||
chr2:241339370
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.594+1580C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339370 | ||||||
chr2:241339375
|
G | GA | 25 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(22): Show | 31 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.594+1597dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339375 | |||||
chr2:241339703
|
G | A | 30 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(27): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.594+1913G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339703 | ||||||
chr2:241339898
|
G | C | 1 | a0001c0001t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.594+2108G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339898 | ||||||
chr2:241339942
|
G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.594+2152G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339942 | ||||||
chr2:241340027
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0122 | 2 | HG00733.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.594+2237G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340027 | ||||||
chr2:241340150
|
C | T | 1 | a0001c0001t0021g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.594+2360C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340150 | ||||||
chr2:241340324
|
C | T | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.594+2534C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340324 | ||||||
chr2:241340338
|
T | C | 1 | a0001c0001t0016g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.594+2548T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340338 | ||||||
chr2:241340565
|
T | G | 15 | a0001c0001t0002g0016a0001c0001t0006g0296a0001c0001t0006g0303others(12): Show | 17 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.595-2427T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340565 | ||||||
chr2:241340568
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(240): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.595-2424T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340568 | ||||||
chr2:241340656
|
T | C | 2 | a0001c0001t0002g0261a0001c0001t0002g0262 | 2 | NA18949.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.595-2336T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340656 | ||||||
chr2:241340696
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.595-2296A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340696 | ||||||
chr2:241340735
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-2257C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340735 | ||||||
chr2:241340937
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.595-2055T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340937 | ||||||
chr2:241341111
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.595-1881T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341111 | ||||||
chr2:241341134
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.595-1858C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341134 | ||||||
chr2:241341393
|
T | G | 2 | a0001c0001t0007g0181a0001c0001t0007g0182 | 2 | HG03927.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.595-1599T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341393 | ||||||
chr2:241341394
|
TACTA | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.595-1594_595-1591d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241341394 | |||||
chr2:241341410
|
A | G | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.595-1582A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341410 | ||||||
chr2:241341420
|
C | T | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.595-1572C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341420 | ||||||
chr2:241341508
|
C | T | 4 | a0001c0001t0004g0034a0001c0001t0004g0082a0001c0001t0004g0157others(1): Show | 5 | HG00639.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-1484C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341508 | ||||||
chr2:241341509
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.595-1483G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341509 | ||||||
chr2:241341569
|
A | T | 1 | a0001c0001t0006g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.595-1423A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341569 | ||||||
chr2:241341688
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.595-1304T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341688 | ||||||
chr2:241342000
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.595-992C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342000 | ||||||
chr2:241342023
|
T | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.595-969T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342023 | ||||||
chr2:241342028
|
T | C | 1 | a0001c0002t0008g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.595-964T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342028 | ||||||
chr2:241342185
|
T | C | 30 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(27): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.595-807T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342185 | ||||||
chr2:241342225
|
C | T | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.595-767C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342225 | ||||||
chr2:241342314
|
C | G | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-678C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342314 | ||||||
chr2:241342319
|
G | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.595-673G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342319 | ||||||
chr2:241342373
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.595-619T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342373 | ||||||
chr2:241342534
|
A | AT | 44 | a0001c0001t0002g0061a0001c0001t0002g0066a0001c0001t0002g0253others(41): Show | 54 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.595-434dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | |||||
chr2:241342534
|
A | ATT | 30 | a0001c0001t0002g0016a0001c0001t0003g0203a0001c0001t0003g0227others(27): Show | 36 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.595-435_595-434dup others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | |||||
chr2:241342534
|
AT | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(110): Show | 148 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.595-434delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | |||||
chr2:241342564
|
G | A | 1 | a0001c0001t0002g0261 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.595-428G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342564 | ||||||
chr2:241342577
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.595-415G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342577 | ||||||
chr2:241342788
|
G | A | 10 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0053others(7): Show | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-204G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342788 | ||||||
chr2:241342832
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.595-160G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342832 | ||||||
chr2:241342947
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.595-45A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342947 | ||||||
chr2:241342950
|
C | A | 1 | a0001c0001t0003g0217 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.595-42C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342950 | ||||||
chr2:241343167
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.696+74G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343167 | ||||||
chr2:241343207
|
T | A | 1 | a0001c0001t0005g0209 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.696+114T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343207 | ||||||
chr2:241343308
|
G | A | 1 | a0001c0001t0007g0035 | 2 | HG00423.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.696+215G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343308 | ||||||
chr2:241343431
|
A | G | 1 | a0001c0001t0011g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697-321A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343431 | ||||||
chr2:241343497
|
CA | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0118a0001c0001t0008g0030others(9): Show | 14 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-241delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 241343497 | |||||
chr2:241343542
|
A | T | 69 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(66): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.697-210A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343542 | ||||||
chr2:241343656
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(251): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.697-96C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343656 | ||||||
chr2:241343679
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(240): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.697-73A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343679 | ||||||
chr2:241343708
|
G | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.697-44G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343708 | ||||||
chr2:241343730
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.697-22T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343730 | ||||||
chr2:241343936
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.842+39G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241343936 | ||||||
chr2:241343937
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.842+40T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241343937 | ||||||
chr2:241344007
|
C | T | 1 | a0001c0001t0007g0187 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.842+110C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344007 | ||||||
chr2:241344008
|
G | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | NA18939.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+111G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344008 | ||||||
chr2:241344139
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.842+242C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344139 | ||||||
chr2:241344158
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.842+261C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344158 | ||||||
chr2:241344264
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.842+367T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344264 | ||||||
chr2:241344381
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.842+484A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344381 | ||||||
chr2:241344391
|
T | C | 1 | a0001c0001t0028g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.842+494T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344391 | ||||||
chr2:241344411
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.842+514T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344411 | ||||||
chr2:241344507
|
A | C | 1 | a0001c0001t0006g0254 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.842+610A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344507 | ||||||
chr2:241344518
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.842+621G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344518 | ||||||
chr2:241344562
|
C | T | 2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.842+665C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344562 | ||||||
chr2:241344576
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.842+679C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344576 | ||||||
chr2:241344600
|
G | C | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.842+703G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344600 | ||||||
chr2:241344633
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.842+736G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344633 | ||||||
chr2:241344751
|
T | C | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.842+854T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344751 | ||||||
chr2:241344811
|
C | T | 1 | a0001c0001t0012g0013 | 3 | HG00741.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.842+914C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344811 | ||||||
chr2:241344878
|
T | TGACATGG others(16): Show |
2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.842+1005_842+1027d others(25): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 241344878 | |||||
chr2:241344882
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.842+985A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344882 | ||||||
chr2:241344989
|
C | T | 2 | a0001c0001t0010g0021a0001c0001t0010g0079 | 3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1092C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344989 | ||||||
chr2:241344990
|
G | A | 24 | a0001c0001t0006g0189a0001c0001t0007g0004a0001c0001t0007g0035others(21): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.842+1093G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344990 | ||||||
chr2:241345077
|
C | T | 1 | a0001c0001t0010g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1089C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345077 | ||||||
chr2:241345230
|
C | T | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.843-936C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345230 | ||||||
chr2:241345231
|
G | A | 10 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0053others(7): Show | 12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.843-935G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345231 | ||||||
chr2:241345365
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.843-801A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345365 | ||||||
chr2:241345409
|
G | A | 73 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(70): Show | 86 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.843-757G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345409 | ||||||
chr2:241345437
|
GACTTT | G | 26 | a0001c0001t0002g0016a0001c0001t0006g0050a0001c0001t0006g0051others(23): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.843-722_843-718del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 241345437 | |||||
chr2:241345606
|
A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843-560A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345606 | ||||||
chr2:241345607
|
T | A | 3 | a0001c0001t0003g0211a0001c0001t0003g0221a0001c0001t0028g0212 | 3 | HG01891.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.843-559T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345607 | ||||||
chr2:241345735
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.843-431A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345735 | ||||||
chr2:241345736
|
T | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01515.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.843-430T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345736 | ||||||
chr2:241345769
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.843-397G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345769 | ||||||
chr2:241345836
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.843-330T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345836 | ||||||
chr2:241345873
|
T | C | 4 | a0001c0001t0002g0081a0001c0001t0002g0253a0001c0001t0002g0265others(1): Show | 4 | HG01106.hp2 HG01192.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-293T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345873 | ||||||
chr2:241345958
|
C | T | 1 | a0001c0001t0007g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843-208C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345958 | ||||||
chr2:241346007
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.843-159G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346007 | ||||||
chr2:241346086
|
T | C | 43 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(40): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.843-80T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346086 | ||||||
chr2:241346102
|
T | C | 7 | a0001c0001t0003g0043a0001c0001t0003g0219a0001c0001t0003g0237others(4): Show | 8 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-64T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346102 | ||||||
chr2:241346125
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.843-41T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346125 | ||||||
chr2:241346130
|
A | G | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.843-36A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346130 | ||||||
chr2:241346528
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.926+279T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346528 | ||||||
chr2:241346592
|
T | A | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.926+343T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346592 | ||||||
chr2:241346592
|
TA | T | 25 | a0001c0001t0004g0164a0001c0001t0005g0207a0001c0001t0006g0189others(22): Show | 30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.926+356delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241346592 | |||||
chr2:241346725
|
C | T | 2 | a0001c0001t0002g0253a0001c0001t0006g0254 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.926+476C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346725 | ||||||
chr2:241346829
|
G | T | 1 | a0001c0001t0006g0312 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.926+580G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346829 | ||||||
chr2:241346933
|
C | T | 1 | a0001c0001t0006g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.926+684C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346933 | ||||||
chr2:241346934
|
G | A | 2 | a0001c0001t0004g0283a0001c0001t0004g0286 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.926+685G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346934 | ||||||
chr2:241346959
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.926+710C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346959 | ||||||
chr2:241346967
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.926+718A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346967 | ||||||
chr2:241346982
|
C | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.926+733C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346982 | ||||||
chr2:241347028
|
G | A | 2 | a0001c0001t0003g0213a0001c0001t0003g0223 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.926+779G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347028 | ||||||
chr2:241347053
|
G | C | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926+804G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347053 | ||||||
chr2:241347082
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.926+833T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347082 | ||||||
chr2:241347176
|
G | A | 1 | a0001c0001t0006g0306 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.926+927G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347176 | ||||||
chr2:241347253
|
A | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.927-881A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347253 | ||||||
chr2:241347332
|
A | G | 64 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(61): Show | 73 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.927-802A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347332 | ||||||
chr2:241347419
|
G | C | 1 | a0001c0001t0003g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.927-715G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347419 | ||||||
chr2:241347459
|
C | T | 3 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0024g0193 | 4 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-675C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347459 | ||||||
chr2:241347560
|
A | G | 1 | a0002c0003t0002g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927-574A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347560 | ||||||
chr2:241347612
|
A | G | 2 | a0001c0001t0004g0162a0001c0001t0004g0169 | 2 | NA18952.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.927-522A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347612 | ||||||
chr2:241347625
|
G | A | 2 | a0001c0001t0012g0013a0001c0001t0012g0029 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-509G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347625 | ||||||
chr2:241347668
|
A | G | 6 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0249others(3): Show | 8 | HG00609.hp1 HG02129.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.927-466A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347668 | ||||||
chr2:241347697
|
G | T | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.927-437G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347697 | ||||||
chr2:241347778
|
T | C | 1 | a0001c0001t0028g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927-356T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347778 | ||||||
chr2:241347885
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.927-249C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347885 | ||||||
chr2:241347920
|
T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.927-214T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347920 | ||||||
chr2:241348072
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(146): Show | 191 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.927-62T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241348072 | ||||||
chr2:241348475
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(70): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.984+284C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241348475 | ||||||
chr2:241348626
|
TGAG | T | 2 | a0001c0001t0016g0049a0001c0001t0016g0299 | 3 | HG01884.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.984+441_984+443del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241348626 | |||||
chr2:241348745
|
CAATTT | C | 5 | a0001c0001t0010g0072a0001c0001t0011g0019a0001c0001t0011g0071others(2): Show | 6 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+556_984+560del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241348745 | |||||
chr2:241349020
|
C | G | 2 | a0001c0001t0014g0242a0001c0001t0022g0243 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.984+829C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349020 | ||||||
chr2:241349049
|
A | G | 1 | a0001c0001t0003g0222 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.984+858A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349049 | ||||||
chr2:241349235
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0277 | 2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.985-838G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349235 | ||||||
chr2:241349368
|
C | CT | 3 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0278 | 3 | HG00438.hp2 HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.985-702dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241349368 | |||||
chr2:241349371
|
T | TA | 6 | a0001c0001t0001g0125a0001c0001t0007g0035a0001c0001t0007g0179others(3): Show | 7 | HG00140.hp1 HG00423.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-689dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241349371 | |||||
chr2:241349381
|
A | AT | 34 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0024others(31): Show | 42 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-692_985-691ins others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349381 | ||||||
chr2:241349381
|
A | T | 54 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(51): Show | 63 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.985-692A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349381 | ||||||
chr2:241349383
|
A | AT | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(72): Show | 103 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.985-690_985-689ins others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349383 | ||||||
chr2:241349383
|
A | T | 143 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0024others(140): Show | 169 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.985-690A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349383 | ||||||
chr2:241349385
|
T | A | 1 | a0001c0001t0003g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.985-688T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349385 | ||||||
chr2:241349604
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0129 | 2 | NA18943.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.985-469C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349604 | ||||||
chr2:241349636
|
T | C | 23 | a0001c0001t0007g0004a0001c0001t0007g0035a0001c0001t0007g0036others(20): Show | 29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.985-437T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349636 | ||||||
chr2:241349649
|
C | T | 1 | a0001c0001t0002g0016 | 3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.985-424C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349649 | ||||||
chr2:241349650
|
G | A | 8 | a0001c0001t0010g0021a0001c0001t0010g0072a0001c0001t0010g0079others(5): Show | 10 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.985-423G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349650 | ||||||
chr2:241349736
|
G | A | 4 | a0001c0001t0006g0037a0001c0001t0006g0194a0001c0001t0006g0195others(1): Show | 5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-337G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349736 | ||||||
chr2:241350004
|
A | G | 44 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0033others(41): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.985-69A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241350004 | ||||||
chr2:241350248
|
C | CATT | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(252): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.*29+46_*29+48dupAT others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 241350248 | |||||
chr2:241350410
|
G | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 45 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.*29+207G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350410 | ||||||
chr2:241350428
|
A | T | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0044others(49): Show | 59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.*29+225A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350428 | ||||||
chr2:241350476
|
C | CTAAGCTT others(3): Show |
1 | a0001c0001t0002g0277 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.*29+274_*29+283dup others(10): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 241350476 | |||||
chr2:241350632
|
C | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.*29+429C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350632 | ||||||
chr2:241350632
|
C | T | 3 | a0001c0001t0009g0153a0001c0001t0009g0167a0001c0001t0009g0170 | 3 | HG00597.hp1 NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.*29+429C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350632 | ||||||
chr2:241350633
|
A | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.*29+430A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350633 | ||||||
chr2:241350723
|
G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*29+520G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350723 | ||||||
chr2:241350913
|
A | C | 1 | a0001c0001t0002g0069 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.*29+710A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350913 | ||||||
chr2:241350970
|
G | C | 1 | a0001c0001t0005g0196 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*29+767G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350970 | ||||||
chr2:241351059
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*29+856C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351059 | ||||||
chr2:241351339
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.*30-628A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351339 | ||||||
chr2:241351342
|
C | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.*30-625C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351342 | ||||||
chr2:241351752
|
A | C | 4 | a0001c0001t0004g0282a0001c0001t0004g0285a0001c0001t0004g0292others(1): Show | 4 | HG00621.hp1 HG01192.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.*30-215A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351752 |