geneid | 346288 |
---|---|
ensemblid | ENSG00000154997.9 |
hgncid | 33280 |
symbol | SEPTIN14 |
name | septin 14 |
refseq_nuc | NM_207366.3 |
refseq_prot | NP_997249.2 |
ensembl_nuc | ENST00000388975.4 |
ensembl_prot | ENSP00000373627.3 |
mane_status | MANE Select |
chr | chr7 |
start | 55793540 |
end | 55862752 |
strand | - |
ver | v1.2 |
region | chr7:55793540-55862752 |
region5000 | chr7:55788540-55867752 |
regionname0 | SEPTIN14_chr7_55793540_55862752 |
regionname5000 | SEPTIN14_chr7_55788540_55867752 |
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 | 432 | 373 | 88 | 59 | 167 | 15 | 42 | 126 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0002 | 0/0 | 432 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0003 | 0/0 | 432 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0004 | 0/0 | 432 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0005 | 0/0 | 432 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0006 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0007 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0008 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0009 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0010 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
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 | 1299 | 370 | 87 | 59 | 166 | 15 | 41 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0002 | 0/0 | 1299 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0003 | 0/0 | 1299 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0004 | 0/0 | 1299 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0005 | 0/0 | 1299 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0006 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0007 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0008 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0009 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0011 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0012 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
c0013 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
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 | 2454 | 91 | 14 | 7 | 60 | 2 | 8 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0002 | 0/0 | 2453 | 60 | 4 | 10 | 30 | 5 | 11 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0003 | 0/0 | 2453 | 42 | 9 | 4 | 26 | 3 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0004 | 0/0 | 2454 | 41 | 4 | 15 | 11 | 3 | 8 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0005 | 1/1 | 2454 | 33 | 6 | 11 | 9 | 1 | 4 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0006 | 0/0 | 2454 | 28 | 25 | 3 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0007 | 0/0 | 2454 | 7 | 0 | 2 | 3 | 0 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0008 | 0/0 | 2453 | 6 | 0 | 0 | 5 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0009 | 0/0 | 2455 | 6 | 1 | 0 | 3 | 0 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0010 | 0/0 | 2454 | 6 | 0 | 3 | 2 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0011 | 0/0 | 2452 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0012 | 0/0 | 2455 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0013 | 0/0 | 2454 | 4 | 1 | 0 | 3 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0014 | 0/0 | 2455 | 4 | 0 | 1 | 2 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0015 | 0/0 | 2454 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0016 | 0/0 | 2454 | 4 | 0 | 0 | 3 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0017 | 0/0 | 2454 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0018 | 0/0 | 2453 | 4 | 0 | 0 | 1 | 1 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0019 | 0/0 | 2453 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0020 | 0/0 | 2453 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0021 | 0/0 | 2454 | 3 | 0 | 2 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0022 | 0/0 | 2454 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0023 | 0/0 | 2455 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0024 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0025 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0026 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0027 | 0/0 | 2452 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0028 | 0/0 | 2453 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0029 | 0/0 | 2453 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0030 | 0/0 | 2452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0031 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0032 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0033 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0034 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0035 | 0/0 | 2452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0036 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0037 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0038 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0039 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0040 | 0/0 | 2454 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
t0041 | 0/0 | 2453 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
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 | 1299 | 370 | 87 | 59 | 166 | 15 | 41 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0006 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0011 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0012 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0002c0002 | 0/0 | 1299 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0003c0003 | 0/0 | 1299 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0004c0005 | 0/0 | 1299 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0005c0004 | 0/0 | 1299 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0006c0013 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0007c0008 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0008c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0009c0009 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0010c0007 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3752 | 90 | 14 | 7 | 60 | 2 | 7 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0002 | 0/0 | 3751 | 59 | 4 | 10 | 29 | 5 | 11 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0003 | 0/0 | 3751 | 38 | 9 | 2 | 25 | 2 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0004 | 0/0 | 3752 | 41 | 4 | 15 | 11 | 3 | 8 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0005 | 1/1 | 3752 | 32 | 5 | 11 | 9 | 1 | 4 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0006 | 0/0 | 3752 | 26 | 23 | 3 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0007 | 0/0 | 3752 | 7 | 0 | 2 | 3 | 0 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0008 | 0/0 | 3751 | 6 | 0 | 0 | 5 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0009 | 0/0 | 3753 | 5 | 0 | 0 | 3 | 0 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0010 | 0/0 | 3752 | 4 | 0 | 1 | 2 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0011 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0012 | 0/0 | 3753 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0013 | 0/0 | 3752 | 4 | 1 | 0 | 3 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0014 | 0/0 | 3753 | 4 | 0 | 1 | 2 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0015 | 0/0 | 3752 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0016 | 0/0 | 3752 | 4 | 0 | 0 | 3 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0017 | 0/0 | 3752 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0018 | 0/0 | 3751 | 4 | 0 | 0 | 1 | 1 | 2 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0020 | 0/0 | 3751 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0021 | 0/0 | 3752 | 3 | 0 | 2 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0022 | 0/0 | 3752 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0023 | 0/0 | 3753 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0024 | 0/0 | 3752 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0025 | 0/0 | 3752 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0026 | 0/0 | 3752 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0027 | 0/0 | 3750 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0028 | 0/0 | 3751 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0029 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0030 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0031 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0032 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0033 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0034 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0035 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0036 | 0/0 | 3752 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0037 | 0/0 | 3752 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0038 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0040 | 0/0 | 3752 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0001t0041 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0006t0005 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0011t0001 | 0/0 | 3752 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0001c0012t0002 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0002c0002t0003 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0002c0002t0011 | 0/0 | 3750 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0003c0003t0019 | 0/0 | 3751 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0004c0005t0010 | 0/0 | 3752 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0005c0004t0003 | 0/0 | 3751 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0006c0013t0039 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0007c0008t0006 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0008c0010t0003 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0009c0009t0006 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
a0010c0007t0009 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | copy fasta | chr7 | 55788540 | 55867752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0002g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0004g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0006g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0009g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0009g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0009g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0009g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0010g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0011g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0012g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0012g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0014g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0014g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0014g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0016g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0016g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0018g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0018g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0018g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0018g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0020g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0020g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0020g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0021g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0021g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0021g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0022g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0022g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0023g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0023g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0024g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0024g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0025g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0025g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0026g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0026g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0027g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0028g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0028g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0029g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0030g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0031g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0032g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0033g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0034g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0035g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0036g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0037g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0038g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0040g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0001t0041g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0006t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0011t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0001c0012t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0002c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0002c0002t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0002c0002t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0002c0002t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0002c0002t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0003c0003t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0003c0003t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0003c0003t0019g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0004c0005t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0004c0005t0010g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0005c0004t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0005c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0006c0013t0039g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0007c0008t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0008c0010t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0009c0009t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
a0010c0007t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | GBR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00099 | hp2 | a0005 | c0004 | t0003 | g0070 | EUR | GBR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | GBR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0141 | EUR | GBR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0249 | EUR | FIN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00280 | hp2 | a0001 | c0001 | t0018 | g0325 | EUR | FIN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0166 | EUR | FIN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | FIN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0373 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0381 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00609 | hp2 | a0001 | c0001 | t0023 | g0230 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0277 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00673 | hp2 | a0001 | c0001 | t0031 | g0227 | EAS | CHS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01106 | hp2 | a0001 | c0001 | t0029 | g0026 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01109 | hp1 | a0003 | c0003 | t0019 | g0004 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0327 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0138 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01175 | hp2 | a0001 | c0001 | t0023 | g0195 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01192 | hp1 | a0005 | c0004 | t0003 | g0049 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PUR | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01256 | hp1 | a0001 | c0001 | t0021 | g0123 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01256 | hp2 | a0004 | c0005 | t0010 | g0158 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01258 | hp2 | a0001 | c0001 | t0021 | g0122 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01261 | hp1 | a0004 | c0005 | t0010 | g0157 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0177 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0378 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01358 | hp2 | a0001 | c0001 | t0041 | g0104 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0083 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0169 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01516 | hp2 | a0001 | c0001 | t0040 | g0113 | EUR | IBS | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01891 | hp1 | a0001 | c0001 | t0027 | g0103 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0387 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0389 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01981 | hp1 | a0001 | c0001 | t0036 | g0261 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0385 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01993 | hp1 | a0001 | c0001 | t0028 | g0131 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02040 | hp1 | a0008 | c0010 | t0003 | g0067 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02080 | hp1 | a0001 | c0001 | t0022 | g0031 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02145 | hp1 | a0001 | c0001 | t0024 | g0298 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CDX | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CDX | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CDX | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02257 | hp2 | a0002 | c0002 | t0011 | g0005 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02258 | hp2 | a0007 | c0008 | t0006 | g0088 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0086 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0371 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0093 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0365 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02622 | hp1 | a0003 | c0003 | t0019 | g0002 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0320 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02630 | hp1 | a0001 | c0001 | t0030 | g0076 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02647 | hp1 | a0001 | c0001 | t0017 | g0078 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0302 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02683 | hp1 | a0001 | c0011 | t0001 | g0255 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02683 | hp2 | a0001 | c0001 | t0021 | g0136 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02698 | hp2 | a0001 | c0001 | t0018 | g0253 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02735 | hp2 | a0001 | c0001 | t0018 | g0358 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02738 | hp1 | a0001 | c0001 | t0007 | g0151 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0181 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02809 | hp2 | a0002 | c0002 | t0011 | g0009 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0092 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0368 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0354 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0366 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0340 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02922 | hp1 | a0002 | c0002 | t0011 | g0010 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02922 | hp2 | a0006 | c0013 | t0039 | g0008 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02970 | hp1 | a0001 | c0001 | t0033 | g0251 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0085 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0367 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0376 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03098 | hp1 | a0001 | c0001 | t0025 | g0388 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0362 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0260 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0364 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03209 | hp2 | a0001 | c0001 | t0038 | g0100 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03225 | hp2 | a0002 | c0002 | t0011 | g0006 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03453 | hp1 | a0001 | c0001 | t0026 | g0361 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03486 | hp1 | a0001 | c0001 | t0027 | g0102 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03492 | hp2 | a0001 | c0001 | t0009 | g0363 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03540 | hp2 | a0003 | c0003 | t0019 | g0003 | AFR | GWD | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0268 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0150 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0114 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0198 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0124 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03927 | hp1 | a0001 | c0001 | t0016 | g0193 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0107 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0108 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0197 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0135 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0015 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | STU | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0098 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | CHB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18747 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | CHB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18906 | hp1 | a0001 | c0001 | t0035 | g0101 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18939 | hp1 | a0001 | c0001 | t0020 | g0213 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0384 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18940 | hp1 | a0001 | c0001 | t0016 | g0243 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0380 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18943 | hp1 | a0001 | c0001 | t0016 | g0192 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18944 | hp2 | a0001 | c0001 | t0009 | g0289 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18952 | hp2 | a0001 | c0001 | t0010 | g0012 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18953 | hp2 | a0001 | c0001 | t0018 | g0347 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18954 | hp2 | a0001 | c0001 | t0013 | g0050 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18961 | hp1 | a0001 | c0001 | t0020 | g0190 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18966 | hp1 | a0001 | c0001 | t0007 | g0209 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18966 | hp2 | a0001 | c0001 | t0037 | g0332 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18975 | hp1 | a0001 | c0001 | t0014 | g0370 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18975 | hp2 | a0001 | c0001 | t0034 | g0189 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18984 | hp2 | a0001 | c0001 | t0016 | g0204 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18986 | hp2 | a0001 | c0001 | t0022 | g0041 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18989 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18989 | hp2 | a0001 | c0001 | t0008 | g0183 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19000 | hp1 | a0001 | c0001 | t0014 | g0106 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19000 | hp2 | a0001 | c0001 | t0013 | g0024 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19010 | hp2 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19012 | hp1 | a0001 | c0001 | t0013 | g0028 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0080 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19030 | hp2 | a0010 | c0007 | t0009 | g0271 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0386 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19058 | hp1 | a0001 | c0001 | t0028 | g0379 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0377 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19068 | hp2 | a0001 | c0012 | t0002 | g0203 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19072 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19075 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0383 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19087 | hp1 | a0001 | c0001 | t0020 | g0219 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19240 | hp1 | a0001 | c0001 | t0024 | g0352 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | YRI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | ASW | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | ASW | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0132 | EUR | TSI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | TSI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0321 | EUR | TSI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0127 | EUR | TSI | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | GIH | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0118 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0375 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02486 | hp2 | a0009 | c0009 | t0006 | g0096 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03471 | hp1 | a0001 | c0001 | t0032 | g0356 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG03471 | hp2 | a0001 | c0001 | t0017 | g0094 | AFR | MSL | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0307 | AFR | USA | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | USA | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | USA | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0382 | AFR | USA | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
NA21309 | hp2 | a0001 | c0006 | t0005 | g0121 | AFR | LWK | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0232 | REF | REF | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0134 | REF | REF | SEPTIN14_chr7_55788540_55867752 | SEPTIN14 | chr7 | 55788540 | 55867752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:55805350
|
C | T | 1 | a0008 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1027G>A | p.Asp343Asn | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/10 | 1107/3752 | 1027/1299 | 343/432 | chr7 | 55805350 | ||
chr7:55807118
|
C | T | 1 | a0009 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.958G>A | p.Asp320Asn | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/10 | 1038/3752 | 958/1299 | 320/432 | chr7 | 55807118 | ||
chr7:55843057
|
C | T | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.443G>A | p.Arg148His | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/10 | 523/3752 | 443/1299 | 148/432 | chr7 | 55843057 | ||
chr7:55843082
|
G | T | 1 | a0003 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.418C>A | p.Leu140Ile | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/10 | 498/3752 | 418/1299 | 140/432 | chr7 | 55843082 | ||
chr7:55844615
|
A | C | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.279T>G | p.Ile93Met | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/10 | 359/3752 | 279/1299 | 93/432 | chr7 | 55844615 | ||
chr7:55844652
|
T | C | 1 | a0004 | 2 | HG01256.hp2 HG01261.hp1 |
missense_variant | MODERATE | c.242A>G | p.Lys81Arg | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/10 | 322/3752 | 242/1299 | 81/432 | chr7 | 55844652 | ||
chr7:55846558
|
C | G | 1 | a0005 | 2 | HG00099.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.134G>C | p.Arg45Thr | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/10 | 214/3752 | 134/1299 | 45/432 | chr7 | 55846558 | ||
chr7:55861987
|
T | C | 1 | a0006 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.10A>G | p.Arg4Gly | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/10 | 90/3752 | 10/1299 | 4/432 | chr7 | 55861987 | ||
chr7:55861993
|
C | T | 1 | a0002 | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.4G>A | p.Ala2Thr | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/10 | 84/3752 | 4/1299 | 2/432 | chr7 | 55861993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:55843029
|
G | A | 1 | a0001c0011 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.471C>T | p.Arg157Arg | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/10 | 551/3752 | 471/1299 | 157/432 | chr7 | 55843029 | ||
chr7:55843041
|
G | A | 1 | a0001c0012 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.459C>T | p.Tyr153Tyr | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/10 | 539/3752 | 459/1299 | 153/432 | chr7 | 55843041 | ||
chr7:55844696
|
C | T | 1 | a0001c0006 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.198G>A | p.Ser66Ser | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/10 | 278/3752 | 198/1299 | 66/432 | chr7 | 55844696 | ||
chr7:55844714
|
C | T | 1 | a0006c0013 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.180G>A | p.Glu60Glu | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/10 | 260/3752 | 180/1299 | 60/432 | chr7 | 55844714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:55793553
|
C | T | 1 | a0006c0013t0039 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2360G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 2360 | chr7 | 55793553 | |||||
chr7:55793690
|
G | C | 1 | a0001c0001t0036 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 2223 | chr7 | 55793690 | |||||
chr7:55793742
|
T | C | 1 | a0001c0001t0021 | 3 | HG01256.hp1 HG01258.hp2 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2171A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 2171 | chr7 | 55793742 | |||||
chr7:55793787
|
G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2126C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 2126 | chr7 | 55793787 | |||||
chr7:55793820
|
A | G | 4 | a0001c0001t0004a0001c0001t0014a0001c0001t0021others(1): Show | 50 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2093T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 2093 | chr7 | 55793820 | |||||
chr7:55794043
|
A | G | 1 | a0006c0013t0039 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1870T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1870 | chr7 | 55794043 | |||||
chr7:55794050
|
T | C | 1 | a0001c0001t0037 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1863A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1863 | chr7 | 55794050 | |||||
chr7:55794060
|
A | C | 1 | a0001c0001t0024 | 2 | HG02145.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1853T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1853 | chr7 | 55794060 | |||||
chr7:55794146
|
T | C | 4 | a0001c0001t0006a0001c0001t0017a0007c0008t0006others(1): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1767A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1767 | chr7 | 55794146 | |||||
chr7:55794147
|
G | A | 1 | a0001c0001t0017 | 4 | HG02615.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1766 | chr7 | 55794147 | |||||
chr7:55794546
|
TAG | T | 5 | a0001c0001t0011a0001c0001t0027a0001c0001t0030others(2): Show | 9 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1365_*1366delCT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1365 | chr7 | 55794546 | |||||
chr7:55794622
|
T | C | 2 | a0001c0001t0008a0001c0001t0022 | 8 | HG02056.hp1 HG02080.hp1 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1291A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1291 | chr7 | 55794622 | |||||
chr7:55794624
|
T | C | 2 | a0001c0001t0008a0001c0001t0022 | 8 | HG02056.hp1 HG02080.hp1 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1289A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1289 | chr7 | 55794624 | |||||
chr7:55794652
|
A | G | 3 | a0001c0001t0024a0001c0001t0025a0001c0001t0026 | 6 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1261T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1261 | chr7 | 55794652 | |||||
chr7:55794682
|
G | A | 12 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(9): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1231C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1231 | chr7 | 55794682 | |||||
chr7:55794692
|
C | A | 1 | a0001c0001t0038 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1221G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1221 | chr7 | 55794692 | |||||
chr7:55794701
|
A | C | 1 | a0001c0001t0020 | 3 | NA18939.hp1 NA18961.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1212T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1212 | chr7 | 55794701 | |||||
chr7:55794857
|
G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1056 | chr7 | 55794857 | |||||
chr7:55794873
|
G | A | 4 | a0001c0001t0006a0001c0001t0017a0007c0008t0006others(1): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1040C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 1040 | chr7 | 55794873 | |||||
chr7:55794964
|
C | CT | 1 | a0001c0001t0012 | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*948dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 948 | chr7 | 55794964 | |||||
chr7:55795006
|
T | C | 1 | a0001c0001t0029 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 907 | chr7 | 55795006 | |||||
chr7:55795151
|
C | T | 8 | a0001c0001t0006a0001c0001t0017a0001c0001t0027others(5): Show | 37 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*762G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 762 | chr7 | 55795151 | |||||
chr7:55795268
|
G | T | 5 | a0001c0001t0010a0001c0001t0016a0001c0001t0031others(2): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*645C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 645 | chr7 | 55795268 | |||||
chr7:55795343
|
T | C | 2 | a0001c0001t0016a0001c0001t0034 | 5 | HG03927.hp1 NA18940.hp1 NA18943.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*570A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 570 | chr7 | 55795343 | |||||
chr7:55795381
|
A | C | 7 | a0001c0001t0006a0001c0001t0017a0001c0001t0027others(4): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*532T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 532 | chr7 | 55795381 | |||||
chr7:55795404
|
G | A | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0020others(1): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*509C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 509 | chr7 | 55795404 | |||||
chr7:55795430
|
G | T | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(28): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 483 | chr7 | 55795430 | |||||
chr7:55795441
|
T | A | 1 | a0001c0001t0026 | 2 | HG02486.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 472 | chr7 | 55795441 | |||||
chr7:55795462
|
C | CT | 8 | a0001c0001t0009a0001c0001t0014a0001c0001t0023others(5): Show | 16 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*450dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 450 | chr7 | 55795462 | |||||
chr7:55795462
|
CT | C | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(10): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*450delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 450 | chr7 | 55795462 | |||||
chr7:55795463
|
T | C | 7 | a0001c0001t0006a0001c0001t0017a0001c0001t0027others(4): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 450 | chr7 | 55795463 | |||||
chr7:55795559
|
C | T | 1 | a0001c0001t0030 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 354 | chr7 | 55795559 | |||||
chr7:55795572
|
A | C | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(10): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 341 | chr7 | 55795572 | |||||
chr7:55795615
|
C | T | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0020others(1): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*298G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 298 | chr7 | 55795615 | |||||
chr7:55795795
|
T | C | 2 | a0001c0001t0040a0001c0001t0041 | 2 | HG01358.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*118A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 10/10 | 118 | chr7 | 55795795 | |||||
chr7:55862703
|
G | T | 1 | a0003c0003t0019 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/10 | chr7 | 55862703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:55796325
|
G | A | 3 | a0001c0001t0017g0078a0001c0001t0017g0092a0001c0001t0017g0093 | 3 | HG02615.hp1 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1120-233C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796325 | ||||||
chr7:55796385
|
C | T | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-293G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796385 | ||||||
chr7:55796648
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1120-556G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796648 | ||||||
chr7:55796685
|
C | T | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-593G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796685 | ||||||
chr7:55796686
|
A | G | 188 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1120-594T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796686 | ||||||
chr7:55796695
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1120-603C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796695 | ||||||
chr7:55796704
|
C | T | 1 | a0003c0003t0019g0002 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1120-612G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796704 | ||||||
chr7:55796890
|
C | T | 2 | a0001c0001t0040g0113a0001c0001t0041g0104 | 2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1120-798G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796890 | ||||||
chr7:55796968
|
C | G | 5 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086others(2): Show | 5 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-876G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55796968 | ||||||
chr7:55797054
|
C | T | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1120-962G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797054 | ||||||
chr7:55797067
|
A | G | 188 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1120-975T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797067 | ||||||
chr7:55797071
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1120-979G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797071 | ||||||
chr7:55797077
|
C | T | 116 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1120-985G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797077 | ||||||
chr7:55797114
|
C | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0033a0001c0001t0002g0063 | 3 | HG00544.hp1 HG00609.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1120-1022G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797114 | ||||||
chr7:55797138
|
A | G | 29 | a0001c0001t0004g0001a0001c0001t0004g0105a0001c0001t0004g0109others(26): Show | 30 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.1120-1046T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797138 | ||||||
chr7:55797148
|
G | A | 58 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1120-1056C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797148 | ||||||
chr7:55797490
|
A | C | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-1398T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797490 | ||||||
chr7:55797790
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1120-1698C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797790 | ||||||
chr7:55797854
|
A | G | 188 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1120-1762T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797854 | ||||||
chr7:55797913
|
C | A | 10 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0275others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1120-1821G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797913 | ||||||
chr7:55797916
|
A | C | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1120-1824T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797916 | ||||||
chr7:55797980
|
C | T | 1 | a0001c0001t0016g0192 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1120-1888G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55797980 | ||||||
chr7:55798041
|
C | T | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-1949G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798041 | ||||||
chr7:55798042
|
G | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-1950C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798042 | ||||||
chr7:55798203
|
A | T | 116 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1120-2111T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798203 | ||||||
chr7:55798240
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0047 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1120-2148C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798240 | ||||||
chr7:55798263
|
G | A | 1 | a0001c0001t0007g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1120-2171C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798263 | ||||||
chr7:55798458
|
A | G | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-2366T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798458 | ||||||
chr7:55798459
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1120-2367T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798459 | ||||||
chr7:55798475
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0064 | 2 | NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1120-2383G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798475 | ||||||
chr7:55798510
|
C | T | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1120-2418G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798510 | ||||||
chr7:55798513
|
A | G | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1120-2421T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798513 | ||||||
chr7:55798581
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1120-2489G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798581 | ||||||
chr7:55798604
|
G | A | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1120-2512C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798604 | ||||||
chr7:55798680
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1120-2588A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798680 | ||||||
chr7:55798706
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1120-2614G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798706 | ||||||
chr7:55798750
|
A | G | 29 | a0001c0001t0004g0001a0001c0001t0004g0105a0001c0001t0004g0109others(26): Show | 30 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.1120-2658T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798750 | ||||||
chr7:55798762
|
A | T | 1 | a0001c0001t0006g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1120-2670T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798762 | ||||||
chr7:55798814
|
G | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-2722C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798814 | ||||||
chr7:55798877
|
C | T | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-2785G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798877 | ||||||
chr7:55798924
|
C | T | 9 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(6): Show | 9 | HG00673.hp2 HG03927.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-2832G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55798924 | ||||||
chr7:55799011
|
T | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-2919A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799011 | ||||||
chr7:55799089
|
A | G | 3 | a0003c0003t0019g0002a0003c0003t0019g0003a0003c0003t0019g0004 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1120-2997T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799089 | ||||||
chr7:55799234
|
A | G | 37 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(34): Show | 37 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1120-3142T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799234 | ||||||
chr7:55799273
|
A | G | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1120-3181T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799273 | ||||||
chr7:55799280
|
T | C | 302 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1120-3188A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799280 | ||||||
chr7:55799281
|
G | A | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120-3189C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799281 | ||||||
chr7:55799337
|
C | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-3245G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799337 | ||||||
chr7:55799351
|
C | CA | 9 | a0001c0001t0002g0180a0001c0001t0002g0244a0001c0001t0003g0045others(6): Show | 9 | HG01175.hp2 HG02040.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-3260dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799351 | ||||||
chr7:55799351
|
C | CAAA | 32 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(29): Show | 32 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1120-3262_1120-326 others(7): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799351 | ||||||
chr7:55799351
|
CA | C | 25 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(22): Show | 25 | HG00140.hp2 HG01928.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.1120-3260delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799351 | ||||||
chr7:55799466
|
T | C | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-3374A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799466 | ||||||
chr7:55799518
|
C | A | 1 | a0001c0001t0005g0138 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1120-3426G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
C | CA | 58 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0170others(55): Show | 58 | HG00099.hp1 HG00673.hp2 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.1120-3427dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
C | CAA | 9 | a0001c0001t0002g0244a0001c0001t0005g0187a0001c0001t0006g0011others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-3428_1120-342 others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
CA | C | 10 | a0001c0001t0002g0161a0001c0001t0002g0167a0001c0001t0002g0180others(7): Show | 10 | HG00733.hp1 HG02572.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1120-3427delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
CAAAAAA | C | 6 | a0001c0001t0001g0278a0001c0001t0001g0323a0001c0001t0009g0289others(3): Show | 6 | HG02135.hp2 HG03209.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-3432_1120-342 others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
CAAAAAAA | C | 107 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(104): Show | 107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1120-3433_1120-342 others(11): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799518
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0304 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1120-3439_1120-342 others(17): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799518 | ||||||
chr7:55799565
|
T | C | 304 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1120-3473A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799565 | ||||||
chr7:55799650
|
T | G | 152 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1120-3558A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799650 | ||||||
chr7:55799906
|
A | G | 1 | a0002c0002t0011g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1120-3814T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799906 | ||||||
chr7:55799953
|
G | T | 146 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1120-3861C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55799953 | ||||||
chr7:55800061
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1120-3969C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800061 | ||||||
chr7:55800112
|
A | C | 1 | a0001c0001t0002g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1120-4020T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800112 | ||||||
chr7:55800169
|
A | C | 1 | a0001c0001t0022g0041 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1120-4077T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800169 | ||||||
chr7:55800349
|
C | T | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120-4257G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800349 | ||||||
chr7:55800426
|
C | T | 1 | a0001c0001t0035g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120-4334G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800426 | ||||||
chr7:55800515
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1120-4423A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800515 | ||||||
chr7:55800592
|
C | G | 117 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1120-4500G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800592 | ||||||
chr7:55800610
|
C | T | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120-4518G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800610 | ||||||
chr7:55800623
|
C | CA | 115 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1120-4532dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800623 | ||||||
chr7:55800776
|
A | T | 2 | a0001c0001t0003g0029a0001c0001t0003g0051 | 2 | NA18960.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1119+4482T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800776 | ||||||
chr7:55800890
|
A | C | 118 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(115): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1119+4368T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55800890 | ||||||
chr7:55801114
|
T | C | 117 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1119+4144A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801114 | ||||||
chr7:55801162
|
C | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0299a0002c0002t0011g0005 | 3 | HG00621.hp2 HG02257.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1119+4096G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801162 | ||||||
chr7:55801163
|
G | A | 1 | a0001c0001t0006g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1119+4095C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801163 | ||||||
chr7:55801271
|
G | T | 116 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(113): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1119+3987C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801271 | ||||||
chr7:55801344
|
G | A | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0030g0076others(1): Show | 4 | HG01891.hp1 HG02630.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+3914C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801344 | ||||||
chr7:55801400
|
A | G | 3 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1119+3858T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801400 | ||||||
chr7:55801457
|
G | A | 58 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1119+3801C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801457 | ||||||
chr7:55801783
|
C | T | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+3475G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801783 | ||||||
chr7:55801827
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1119+3431C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801827 | ||||||
chr7:55801877
|
T | C | 117 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1119+3381A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801877 | ||||||
chr7:55801890
|
C | T | 2 | a0001c0001t0006g0083a0001c0001t0006g0097 | 2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1119+3368G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801890 | ||||||
chr7:55801998
|
C | CT | 10 | a0001c0001t0005g0112a0001c0001t0006g0362a0001c0001t0006g0364others(7): Show | 10 | HG01256.hp2 HG01496.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1119+3259dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55801998 | ||||||
chr7:55802031
|
GCT | G | 117 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1119+3225_1119+322 others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802031 | ||||||
chr7:55802067
|
C | T | 1 | a0001c0001t0013g0050 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1119+3191G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802067 | ||||||
chr7:55802068
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1119+3190C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802068 | ||||||
chr7:55802170
|
A | G | 1 | a0001c0001t0032g0356 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1119+3088T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802170 | ||||||
chr7:55802283
|
G | A | 5 | a0001c0001t0002g0152a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+2975C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802283 | ||||||
chr7:55802387
|
A | T | 1 | a0001c0001t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1119+2871T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802387 | ||||||
chr7:55802550
|
G | GA | 151 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1119+2707dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802550 | ||||||
chr7:55802555
|
A | AC | 117 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1119+2702_1119+270 others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802555 | ||||||
chr7:55802620
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1119+2638C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802620 | ||||||
chr7:55802781
|
CA | C | 115 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1119+2476delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802781 | ||||||
chr7:55802788
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1119+2470T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802788 | ||||||
chr7:55802918
|
G | A | 1 | a0001c0001t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1119+2340C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802918 | ||||||
chr7:55802940
|
C | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1119+2318G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802940 | ||||||
chr7:55802940
|
CT | C | 6 | a0001c0001t0002g0179a0001c0001t0004g0384a0001c0001t0008g0046others(3): Show | 6 | HG01256.hp2 HG01261.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119+2317delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55802940 | ||||||
chr7:55803210
|
T | A | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1119+2048A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803210 | ||||||
chr7:55803234
|
G | A | 1 | a0002c0002t0011g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1119+2024C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803234 | ||||||
chr7:55803479
|
A | C | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1119+1779T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803479 | ||||||
chr7:55803569
|
T | C | 1 | a0008c0010t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119+1689A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803569 | ||||||
chr7:55803645
|
C | G | 2 | a0002c0002t0011g0009a0002c0002t0011g0010 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1119+1613G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803645 | ||||||
chr7:55803764
|
G | A | 32 | a0001c0001t0002g0014a0001c0001t0002g0179a0001c0001t0002g0185others(29): Show | 32 | HG00597.hp2 HG02015.hp2 HG02083.hp1 others(29): Show |
intron_variant | MODIFIER | c.1119+1494C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803764 | ||||||
chr7:55803962
|
A | C | 1 | a0001c0001t0017g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1119+1296T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803962 | ||||||
chr7:55803968
|
C | CA | 10 | a0001c0001t0001g0242a0001c0001t0001g0317a0001c0001t0004g0116others(7): Show | 10 | HG02080.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1119+1289dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803968 | ||||||
chr7:55803968
|
CA | C | 142 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1119+1289delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55803968 | ||||||
chr7:55804053
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1119+1205C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804053 | ||||||
chr7:55804092
|
C | T | 1 | a0001c0001t0004g0263 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1119+1166G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804092 | ||||||
chr7:55804107
|
A | G | 387 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(384): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1119+1151T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804107 | ||||||
chr7:55804134
|
T | TA | 53 | a0001c0001t0002g0152a0001c0001t0002g0160a0001c0001t0002g0170others(50): Show | 53 | HG00597.hp1 HG00597.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.1119+1123dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804134 | ||||||
chr7:55804134
|
T | TAA | 97 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1119+1122_1119+112 others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804134 | ||||||
chr7:55804134
|
T | TAAA | 40 | a0001c0001t0001g0242a0001c0001t0001g0250a0001c0001t0001g0256others(37): Show | 40 | HG00673.hp1 HG00673.hp2 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.1119+1121_1119+112 others(7): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804134 | ||||||
chr7:55804134
|
TA | T | 8 | a0001c0001t0002g0216a0001c0001t0003g0066a0001c0001t0005g0112others(5): Show | 8 | HG01496.hp2 HG01993.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1119+1123delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804134 | ||||||
chr7:55804165
|
C | T | 1 | a0002c0002t0011g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1119+1093G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804165 | ||||||
chr7:55804258
|
G | T | 1 | a0001c0001t0001g0353 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1119+1000C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804258 | ||||||
chr7:55804267
|
G | GT | 7 | a0001c0001t0001g0311a0001c0001t0002g0179a0001c0001t0002g0206others(4): Show | 7 | HG00738.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+990dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804267 | ||||||
chr7:55804339
|
A | G | 4 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0199others(1): Show | 4 | HG00609.hp2 HG02145.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+919T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804339 | ||||||
chr7:55804359
|
A | G | 7 | a0001c0001t0004g0001a0001c0001t0004g0110a0001c0001t0004g0125others(4): Show | 8 | HG00639.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1119+899T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804359 | ||||||
chr7:55804479
|
G | A | 2 | a0001c0001t0006g0364a0001c0001t0006g0365 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1119+779C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804479 | ||||||
chr7:55804493
|
A | C | 1 | a0001c0001t0021g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1119+765T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804493 | ||||||
chr7:55804503
|
C | T | 30 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(27): Show | 30 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1119+755G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804503 | ||||||
chr7:55804536
|
G | A | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1119+722C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804536 | ||||||
chr7:55804757
|
G | T | 5 | a0001c0001t0006g0073a0001c0001t0006g0074a0001c0001t0006g0143others(2): Show | 5 | HG01993.hp2 HG02257.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+501C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804757 | ||||||
chr7:55804882
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1119+376T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804882 | ||||||
chr7:55804947
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1119+311G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55804947 | ||||||
chr7:55805046
|
G | T | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+212C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55805046 | ||||||
chr7:55805071
|
C | A | 2 | a0001c0001t0006g0364a0001c0001t0006g0365 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1119+187G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55805071 | ||||||
chr7:55805250
|
G | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.1119+8C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 9/9 | chr7 | 55805250 | ||||||
chr7:55805455
|
G | A | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.987-65C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805455 | ||||||
chr7:55805462
|
T | G | 306 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.987-72A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805462 | ||||||
chr7:55805493
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.987-103C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805493 | ||||||
chr7:55805603
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.987-213T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805603 | ||||||
chr7:55805622
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.987-232G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805622 | ||||||
chr7:55805647
|
AATGGAAA others(15): Show |
A | 1 | a0001c0001t0001g0275 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.987-279_987-258del others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55805647 | ||||||
chr7:55806029
|
C | G | 3 | a0001c0001t0006g0075a0001c0001t0006g0083a0001c0001t0006g0097 | 3 | HG01433.hp1 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.987-639G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806029 | ||||||
chr7:55806122
|
G | C | 1 | a0001c0001t0003g0025 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.987-732C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806122 | ||||||
chr7:55806400
|
C | A | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.986+690G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806400 | ||||||
chr7:55806463
|
T | A | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.986+627A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806463 | ||||||
chr7:55806469
|
C | CT | 152 | a0001c0001t0001g0077a0001c0001t0001g0266a0001c0001t0001g0267others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.986+620dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806469 | ||||||
chr7:55806493
|
T | C | 1 | a0001c0001t0016g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.986+597A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806493 | ||||||
chr7:55806503
|
G | A | 1 | a0001c0001t0023g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.986+587C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806503 | ||||||
chr7:55806758
|
C | T | 1 | a0001c0001t0038g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.986+332G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806758 | ||||||
chr7:55806787
|
A | G | 1 | a0001c0001t0001g0355 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.986+303T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806787 | ||||||
chr7:55806901
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.986+189C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806901 | ||||||
chr7:55806916
|
T | C | 9 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(6): Show | 9 | HG00673.hp2 HG03927.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.986+174A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806916 | ||||||
chr7:55806931
|
C | T | 2 | a0001c0001t0012g0270a0001c0001t0012g0302 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.986+159G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55806931 | ||||||
chr7:55807033
|
T | G | 9 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(6): Show | 9 | HG00673.hp2 HG03927.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.986+57A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 8/9 | chr7 | 55807033 | ||||||
chr7:55807530
|
T | C | 193 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(190): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.818-272A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55807530 | ||||||
chr7:55807645
|
G | C | 1 | a0001c0001t0006g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.818-387C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55807645 | ||||||
chr7:55807739
|
A | G | 1 | a0001c0001t0004g0381 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.818-481T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55807739 | ||||||
chr7:55808065
|
T | G | 24 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(21): Show | 24 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.818-807A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808065 | ||||||
chr7:55808485
|
A | G | 305 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.818-1227T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808485 | ||||||
chr7:55808532
|
T | C | 58 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.818-1274A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808532 | ||||||
chr7:55808615
|
G | A | 1 | a0001c0001t0022g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.818-1357C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808615 | ||||||
chr7:55808772
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0003g0051 | 2 | NA18960.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.818-1514C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808772 | ||||||
chr7:55808843
|
C | T | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.818-1585G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808843 | ||||||
chr7:55808844
|
G | A | 2 | a0001c0001t0006g0364a0001c0001t0006g0365 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.818-1586C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808844 | ||||||
chr7:55808885
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | NA18945.hp1 NA18960.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.818-1627G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55808885 | ||||||
chr7:55809033
|
A | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.818-1775T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809033 | ||||||
chr7:55809038
|
A | T | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.818-1780T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809038 | ||||||
chr7:55809108
|
G | A | 1 | a0001c0001t0024g0352 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.818-1850C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809108 | ||||||
chr7:55809112
|
C | G | 36 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.818-1854G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809112 | ||||||
chr7:55809158
|
G | A | 1 | a0001c0001t0032g0356 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.818-1900C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809158 | ||||||
chr7:55809309
|
C | CT | 29 | a0001c0001t0004g0128a0001c0001t0005g0200a0001c0001t0006g0011others(26): Show | 29 | HG01175.hp2 HG01243.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.818-2052dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809309 | ||||||
chr7:55809309
|
CT | C | 124 | a0001c0001t0001g0256a0001c0001t0001g0314a0001c0001t0001g0318others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.818-2052delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809309 | ||||||
chr7:55809309
|
CTT | C | 6 | a0001c0001t0002g0159a0001c0001t0002g0180a0001c0001t0002g0194others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.818-2053_818-2052d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809309 | ||||||
chr7:55809309
|
CTTT | C | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.818-2054_818-2052d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809309 | ||||||
chr7:55809603
|
T | C | 247 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(244): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.818-2345A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809603 | ||||||
chr7:55809660
|
C | T | 1 | a0001c0001t0030g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.818-2402G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809660 | ||||||
chr7:55809726
|
A | G | 5 | a0001c0001t0011g0376a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.818-2468T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809726 | ||||||
chr7:55809770
|
T | TA | 34 | a0001c0001t0001g0323a0001c0001t0001g0337a0001c0001t0005g0196others(31): Show | 34 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.818-2513dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809770 | ||||||
chr7:55809770
|
TA | T | 77 | a0001c0001t0002g0154a0001c0001t0002g0167a0001c0001t0003g0019others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.818-2513delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809770 | ||||||
chr7:55809786
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-2528T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809786 | ||||||
chr7:55809833
|
CT | C | 192 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.818-2576delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809833 | ||||||
chr7:55809833
|
CTT | C | 110 | a0001c0001t0002g0021a0001c0001t0003g0019a0001c0001t0003g0020others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.818-2577_818-2576d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809833 | ||||||
chr7:55809893
|
C | T | 2 | a0001c0001t0011g0376a0002c0002t0011g0006 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.818-2635G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809893 | ||||||
chr7:55809977
|
C | T | 3 | a0001c0001t0006g0075a0001c0001t0006g0083a0001c0001t0006g0097 | 3 | HG01433.hp1 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.818-2719G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809977 | ||||||
chr7:55809982
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-2724C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55809982 | ||||||
chr7:55810221
|
A | AT | 191 | a0001c0001t0001g0077a0001c0001t0001g0237a0001c0001t0001g0242others(188): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.818-2964dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810221 | ||||||
chr7:55810271
|
C | A | 10 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0275others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.818-3013G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810271 | ||||||
chr7:55810475
|
C | CT | 293 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.818-3218dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810475 | ||||||
chr7:55810475
|
C | CTT | 8 | a0001c0001t0001g0286a0001c0001t0001g0294a0001c0001t0006g0082others(5): Show | 8 | HG01192.hp1 HG01358.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.818-3219_818-3218d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810475 | ||||||
chr7:55810511
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.818-3253C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810511 | ||||||
chr7:55810817
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.818-3559T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55810817 | ||||||
chr7:55811030
|
T | TTTCTTC | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.818-3778_818-3773d others(8): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811030 | ||||||
chr7:55811075
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.818-3817G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811075 | ||||||
chr7:55811081
|
G | A | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.818-3823C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811081 | ||||||
chr7:55811083
|
GT | G | 5 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086others(2): Show | 5 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-3826delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811083 | ||||||
chr7:55811086
|
T | C | 5 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086others(2): Show | 5 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-3828A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811086 | ||||||
chr7:55811100
|
G | C | 1 | a0001c0001t0005g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.818-3842C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811100 | ||||||
chr7:55811264
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0154 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.818-4006G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811264 | ||||||
chr7:55811371
|
T | G | 1 | a0001c0001t0004g0304 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.818-4113A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811371 | ||||||
chr7:55811496
|
C | CT | 72 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0281others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.818-4239dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811496 | ||||||
chr7:55811496
|
CT | C | 86 | a0001c0001t0001g0250a0001c0001t0001g0317a0001c0001t0001g0345others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.818-4239delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811496 | ||||||
chr7:55811496
|
CTT | C | 17 | a0001c0001t0001g0336a0001c0001t0002g0153a0001c0001t0002g0179others(14): Show | 17 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.818-4240_818-4239d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811496 | ||||||
chr7:55811588
|
G | A | 4 | a0001c0001t0001g0280a0001c0001t0004g0127a0001c0001t0004g0132others(1): Show | 4 | HG01099.hp1 HG03669.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-4330C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811588 | ||||||
chr7:55811601
|
A | T | 1 | a0001c0001t0003g0058 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.818-4343T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811601 | ||||||
chr7:55811688
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-4430C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811688 | ||||||
chr7:55811764
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-4506T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811764 | ||||||
chr7:55811847
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-4589C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55811847 | ||||||
chr7:55812275
|
T | C | 2 | a0001c0001t0006g0090a0001c0001t0006g0099 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.818-5017A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812275 | ||||||
chr7:55812431
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.818-5173C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812431 | ||||||
chr7:55812518
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.818-5260C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812518 | ||||||
chr7:55812588
|
G | A | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.818-5330C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812588 | ||||||
chr7:55812731
|
T | C | 1 | a0001c0001t0005g0202 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.818-5473A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812731 | ||||||
chr7:55812750
|
C | T | 1 | a0001c0001t0006g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.818-5492G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812750 | ||||||
chr7:55812756
|
T | C | 193 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(190): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.818-5498A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812756 | ||||||
chr7:55812799
|
C | A | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.818-5541G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812799 | ||||||
chr7:55812886
|
T | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.818-5628A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812886 | ||||||
chr7:55812901
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-5643G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812901 | ||||||
chr7:55812919
|
T | A | 1 | a0001c0001t0005g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.818-5661A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55812919 | ||||||
chr7:55813112
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-5854C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813112 | ||||||
chr7:55813113
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818-5855G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813113 | ||||||
chr7:55813197
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0166 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.817+5930C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813197 | ||||||
chr7:55813232
|
A | G | 244 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(241): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.817+5895T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813232 | ||||||
chr7:55813257
|
G | A | 1 | a0001c0001t0006g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.817+5870C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813257 | ||||||
chr7:55813290
|
C | T | 1 | a0001c0001t0017g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.817+5837G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813290 | ||||||
chr7:55813310
|
G | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.817+5817C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813310 | ||||||
chr7:55813373
|
C | T | 305 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.817+5754G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813373 | ||||||
chr7:55813477
|
C | T | 1 | a0001c0001t0005g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.817+5650G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813477 | ||||||
chr7:55813487
|
G | A | 1 | a0001c0001t0020g0219 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.817+5640C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813487 | ||||||
chr7:55813523
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+5604G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813523 | ||||||
chr7:55813537
|
C | T | 1 | a0001c0001t0005g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817+5590G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813537 | ||||||
chr7:55813538
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.817+5589C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813538 | ||||||
chr7:55813547
|
C | CTCCTTCC others(87): Show |
5 | a0001c0001t0011g0376a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+5486_817+5579d others(96): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813547 | ||||||
chr7:55813691
|
T | G | 5 | a0001c0001t0004g0135a0001c0001t0004g0139a0001c0001t0004g0238others(2): Show | 5 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+5436A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813691 | ||||||
chr7:55813790
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.817+5337T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813790 | ||||||
chr7:55813793
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+5334G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813793 | ||||||
chr7:55813829
|
G | C | 1 | a0001c0001t0013g0050 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.817+5298C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813829 | ||||||
chr7:55813856
|
G | T | 4 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0001g0337others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+5271C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813856 | ||||||
chr7:55813973
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+5154G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813973 | ||||||
chr7:55813994
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+5133A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813994 | ||||||
chr7:55813998
|
G | A | 5 | a0001c0001t0011g0376a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+5129C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55813998 | ||||||
chr7:55814050
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.817+5077A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814050 | ||||||
chr7:55814178
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+4949C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814178 | ||||||
chr7:55814219
|
C | A | 5 | a0001c0001t0011g0376a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+4908G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814219 | ||||||
chr7:55814224
|
A | G | 174 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(171): Show | 174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.817+4903T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814224 | ||||||
chr7:55814225
|
T | A | 174 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(171): Show | 174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.817+4902A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814225 | ||||||
chr7:55814506
|
C | T | 5 | a0001c0001t0006g0073a0001c0001t0006g0074a0001c0001t0006g0143others(2): Show | 5 | HG01993.hp2 HG02257.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+4621G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814506 | ||||||
chr7:55814749
|
A | G | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.817+4378T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814749 | ||||||
chr7:55814845
|
C | T | 3 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.817+4282G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814845 | ||||||
chr7:55814927
|
A | AC | 3 | a0001c0001t0002g0152a0001c0001t0022g0031a0001c0001t0037g0332 | 3 | HG02080.hp1 HG03654.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.817+4199dupG | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55814927 | ||||||
chr7:55815334
|
C | T | 1 | a0001c0001t0009g0289 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.817+3793G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815334 | ||||||
chr7:55815339
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+3788G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815339 | ||||||
chr7:55815391
|
C | T | 1 | a0001c0001t0003g0057 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.817+3736G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815391 | ||||||
chr7:55815468
|
G | A | 5 | a0001c0001t0011g0376a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+3659C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815468 | ||||||
chr7:55815594
|
AG | A | 32 | a0001c0001t0006g0011a0001c0001t0006g0073a0001c0001t0006g0074others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.817+3532delC | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815594 | ||||||
chr7:55815821
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+3306T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815821 | ||||||
chr7:55815888
|
A | G | 70 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0030others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.817+3239T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55815888 | ||||||
chr7:55816125
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+3002A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816125 | ||||||
chr7:55816218
|
G | A | 4 | a0001c0001t0006g0075a0001c0001t0006g0083a0001c0001t0006g0097others(1): Show | 4 | HG01433.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+2909C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816218 | ||||||
chr7:55816254
|
T | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.817+2873A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816254 | ||||||
chr7:55816352
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+2775C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816352 | ||||||
chr7:55816521
|
G | T | 1 | a0001c0001t0009g0268 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.817+2606C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816521 | ||||||
chr7:55816580
|
T | A | 5 | a0001c0001t0004g0304a0001c0001t0004g0305a0001c0001t0004g0306others(2): Show | 5 | HG00733.hp2 HG01255.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+2547A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816580 | ||||||
chr7:55816602
|
T | G | 232 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(229): Show | 232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.817+2525A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816602 | ||||||
chr7:55816633
|
C | T | 23 | a0001c0001t0001g0229a0001c0001t0005g0186a0001c0001t0005g0187others(20): Show | 23 | HG00609.hp2 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.817+2494G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816633 | ||||||
chr7:55816642
|
C | CA | 8 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0002g0184others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.817+2484dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816642 | ||||||
chr7:55816660
|
A | G | 2 | a0001c0001t0010g0012a0001c0001t0010g0016 | 2 | NA18952.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.817+2467T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816660 | ||||||
chr7:55816681
|
C | T | 1 | a0001c0001t0041g0104 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.817+2446G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816681 | ||||||
chr7:55816696
|
A | G | 1 | a0001c0001t0028g0379 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.817+2431T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816696 | ||||||
chr7:55816737
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+2390C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816737 | ||||||
chr7:55816821
|
C | T | 305 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.817+2306G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55816821 | ||||||
chr7:55817076
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.817+2051T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817076 | ||||||
chr7:55817098
|
T | C | 1 | a0001c0001t0005g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817+2029A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817098 | ||||||
chr7:55817142
|
A | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+1985T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817142 | ||||||
chr7:55817151
|
T | C | 31 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.817+1976A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817151 | ||||||
chr7:55817244
|
C | T | 2 | a0001c0001t0003g0055a0001c0001t0003g0072 | 2 | HG01515.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.817+1883G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817244 | ||||||
chr7:55817383
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.817+1744T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817383 | ||||||
chr7:55817386
|
C | A | 1 | a0001c0001t0014g0370 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.817+1741G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817386 | ||||||
chr7:55817460
|
T | TTA | 11 | a0001c0001t0001g0275a0001c0001t0001g0334a0001c0001t0001g0353others(8): Show | 11 | HG00408.hp1 HG02257.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.817+1665_817+1666d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817460 | ||||||
chr7:55817475
|
TA | T | 3 | a0001c0001t0002g0171a0001c0001t0006g0087a0001c0001t0006g0089 | 3 | HG03139.hp1 NA19240.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.817+1651delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817475 | ||||||
chr7:55817476
|
A | AT | 28 | a0001c0001t0001g0250a0001c0001t0001g0256a0001c0001t0001g0258others(25): Show | 28 | HG02015.hp1 HG02027.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.817+1650dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817476 | ||||||
chr7:55817476
|
A | T | 18 | a0001c0001t0002g0147a0001c0001t0002g0165a0001c0001t0002g0175others(15): Show | 18 | HG00140.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.817+1651T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817476 | ||||||
chr7:55817477
|
T | TA | 94 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.817+1649_817+1650i others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817477 | ||||||
chr7:55817478
|
T | A | 78 | a0001c0001t0001g0334a0001c0001t0001g0351a0001c0001t0001g0353others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.817+1649A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817478 | ||||||
chr7:55817479
|
T | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0264a0001c0001t0001g0319others(2): Show | 5 | HG01928.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.817+1648A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817479 | ||||||
chr7:55817480
|
T | A | 1 | a0001c0001t0003g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.817+1647A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817480 | ||||||
chr7:55817606
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+1521T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817606 | ||||||
chr7:55817765
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+1362G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817765 | ||||||
chr7:55817917
|
A | C | 305 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.817+1210T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817917 | ||||||
chr7:55817981
|
G | A | 302 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.817+1146C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55817981 | ||||||
chr7:55818046
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+1081C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818046 | ||||||
chr7:55818131
|
A | G | 16 | a0001c0001t0006g0011a0001c0001t0006g0075a0001c0001t0006g0079others(13): Show | 16 | HG01243.hp2 HG01433.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.817+996T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818131 | ||||||
chr7:55818143
|
A | G | 1 | a0001c0001t0003g0044 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.817+984T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818143 | ||||||
chr7:55818188
|
G | A | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.817+939C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818188 | ||||||
chr7:55818209
|
T | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(3): Show | 6 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+918A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818209 | ||||||
chr7:55818254
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+873G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818254 | ||||||
chr7:55818330
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+797C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818330 | ||||||
chr7:55818341
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+786T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818341 | ||||||
chr7:55818403
|
CAG | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+722_817+723del others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818403 | ||||||
chr7:55818430
|
C | G | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.817+697G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818430 | ||||||
chr7:55818431
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.817+696G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818431 | ||||||
chr7:55818472
|
C | CA | 241 | a0001c0001t0001g0013a0001c0001t0001g0242a0001c0001t0001g0250others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.817+654dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818472 | ||||||
chr7:55818472
|
C | CAA | 45 | a0001c0001t0001g0077a0001c0001t0001g0237a0001c0001t0001g0259others(42): Show | 45 | HG01243.hp1 HG01433.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.817+653_817+654dup others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818472 | ||||||
chr7:55818472
|
C | CAAA | 6 | a0001c0001t0001g0266a0001c0001t0011g0376a0002c0002t0011g0005others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+652_817+654dup others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818472 | ||||||
chr7:55818472
|
CA | C | 9 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0378others(6): Show | 9 | HG00673.hp2 HG01256.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.817+654delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818472 | ||||||
chr7:55818567
|
G | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.817+560C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818567 | ||||||
chr7:55818612
|
C | T | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.817+515G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818612 | ||||||
chr7:55818863
|
T | C | 1 | a0001c0006t0005g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817+264A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55818863 | ||||||
chr7:55819101
|
C | A | 57 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.817+26G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55819101 | ||||||
chr7:55819112
|
C | T | 1 | a0003c0003t0019g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817+15G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 7/9 | chr7 | 55819112 | ||||||
chr7:55819242
|
ATGAAT | A | 4 | a0001c0001t0003g0032a0001c0001t0003g0038a0001c0001t0003g0156others(1): Show | 4 | HG01081.hp2 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-24_721-20delAT others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819242 | ||||||
chr7:55819316
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0047 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.721-93C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819316 | ||||||
chr7:55819445
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0242others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.721-222G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819445 | ||||||
chr7:55819514
|
G | A | 26 | a0001c0001t0001g0242a0001c0001t0001g0262a0001c0001t0001g0264others(23): Show | 26 | HG00408.hp1 HG00621.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.721-291C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819514 | ||||||
chr7:55819583
|
C | T | 6 | a0001c0001t0004g0135a0001c0001t0004g0139a0001c0001t0004g0238others(3): Show | 6 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-360G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819583 | ||||||
chr7:55819584
|
G | A | 1 | a0001c0001t0001g0338 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.721-361C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819584 | ||||||
chr7:55819744
|
GC | G | 302 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.721-522delG | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819744 | ||||||
chr7:55819969
|
T | A | 387 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(384): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.721-746A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819969 | ||||||
chr7:55819988
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0007g0224 | 2 | NA18953.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.721-765A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819988 | ||||||
chr7:55819993
|
C | T | 1 | a0001c0001t0005g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.721-770G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819993 | ||||||
chr7:55819995
|
C | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0009a0002c0002t0011g0010 | 3 | HG02257.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-772G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55819995 | ||||||
chr7:55820131
|
C | T | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.721-908G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820131 | ||||||
chr7:55820153
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.721-930G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820153 | ||||||
chr7:55820243
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-1020A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820243 | ||||||
chr7:55820247
|
C | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-1024G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820247 | ||||||
chr7:55820281
|
G | A | 1 | a0001c0001t0005g0199 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.721-1058C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820281 | ||||||
chr7:55820283
|
G | A | 12 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(9): Show | 12 | HG00673.hp2 HG01256.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.721-1060C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820283 | ||||||
chr7:55820445
|
C | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0009a0002c0002t0011g0010 | 3 | HG02257.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-1222G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820445 | ||||||
chr7:55820631
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-1408C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820631 | ||||||
chr7:55820705
|
C | T | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1482G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820705 | ||||||
chr7:55820944
|
A | G | 17 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0075others(14): Show | 17 | HG01243.hp2 HG01433.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.721-1721T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820944 | ||||||
chr7:55820967
|
C | A | 1 | a0001c0001t0005g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.721-1744G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55820967 | ||||||
chr7:55821101
|
T | C | 1 | a0001c0001t0001g0338 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.721-1878A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821101 | ||||||
chr7:55821124
|
C | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0336 | 2 | HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.721-1901G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821124 | ||||||
chr7:55821174
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-1951G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821174 | ||||||
chr7:55821213
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0242others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.721-1990G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821213 | ||||||
chr7:55821323
|
T | C | 2 | a0001c0001t0004g0128a0001c0001t0004g0141 | 2 | HG00140.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.721-2100A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821323 | ||||||
chr7:55821392
|
C | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0009a0002c0002t0011g0010 | 3 | HG02257.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-2169G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821392 | ||||||
chr7:55821403
|
C | T | 19 | a0001c0001t0004g0124a0001c0001t0004g0135a0001c0001t0004g0139others(16): Show | 19 | HG00544.hp2 HG01123.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.721-2180G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821403 | ||||||
chr7:55821416
|
A | G | 193 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(190): Show | 193 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.721-2193T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821416 | ||||||
chr7:55821587
|
G | T | 1 | a0001c0001t0005g0327 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.721-2364C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821587 | ||||||
chr7:55821631
|
C | CAG | 122 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0242others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.721-2410_721-2409d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821631 | ||||||
chr7:55821641
|
G | A | 184 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.721-2418C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821641 | ||||||
chr7:55821740
|
A | G | 48 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.721-2517T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821740 | ||||||
chr7:55821916
|
C | T | 8 | a0001c0001t0006g0079a0001c0001t0006g0091a0001c0001t0006g0095others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-2693G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55821916 | ||||||
chr7:55822035
|
G | A | 6 | a0001c0001t0001g0266a0001c0001t0001g0284a0001c0001t0001g0286others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-2812C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822035 | ||||||
chr7:55822089
|
T | C | 2 | a0002c0002t0011g0009a0002c0002t0011g0010 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-2866A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822089 | ||||||
chr7:55822309
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-3086A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822309 | ||||||
chr7:55822328
|
C | T | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-3105G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822328 | ||||||
chr7:55822372
|
A | C | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-3149T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822372 | ||||||
chr7:55822469
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0250others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.721-3246T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822469 | ||||||
chr7:55822496
|
GATTCACT others(70): Show |
G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-3350_721-3274d others(79): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822496 | ||||||
chr7:55822830
|
G | A | 1 | a0002c0002t0011g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.721-3607C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822830 | ||||||
chr7:55822836
|
C | G | 9 | a0001c0001t0001g0279a0001c0001t0001g0311a0001c0001t0001g0314others(6): Show | 9 | HG01981.hp1 HG02015.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-3613G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822836 | ||||||
chr7:55822856
|
C | CA | 25 | a0001c0001t0002g0060a0001c0001t0002g0176a0001c0001t0002g0184others(22): Show | 25 | HG00639.hp2 HG00738.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.721-3634dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822856 | ||||||
chr7:55822856
|
C | CAA | 23 | a0001c0001t0001g0229a0001c0001t0004g0238a0001c0001t0004g0239others(20): Show | 23 | HG00609.hp2 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.721-3635_721-3634d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822856 | ||||||
chr7:55822856
|
CA | C | 135 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0250others(132): Show | 135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.721-3634delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55822856 | ||||||
chr7:55823033
|
G | A | 124 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0250others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.721-3810C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823033 | ||||||
chr7:55823129
|
T | A | 1 | a0001c0001t0001g0326 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.721-3906A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823129 | ||||||
chr7:55823154
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.721-3931G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823154 | ||||||
chr7:55823201
|
G | A | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-3978C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823201 | ||||||
chr7:55823278
|
C | A | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-4055G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823278 | ||||||
chr7:55823404
|
C | T | 2 | a0001c0001t0025g0098a0001c0001t0025g0388 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.721-4181G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823404 | ||||||
chr7:55823497
|
T | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | NA18970.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4274A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823497 | ||||||
chr7:55823521
|
G | A | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-4298C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823521 | ||||||
chr7:55823614
|
C | T | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0009others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-4391G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823614 | ||||||
chr7:55823828
|
C | A | 1 | a0001c0001t0018g0358 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.721-4605G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823828 | ||||||
chr7:55823888
|
CT | C | 210 | a0001c0001t0001g0077a0001c0001t0001g0229a0001c0001t0001g0242others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.721-4666delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55823888 | ||||||
chr7:55824073
|
T | G | 26 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(23): Show | 26 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.721-4850A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824073 | ||||||
chr7:55824208
|
C | G | 180 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(177): Show | 180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.721-4985G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824208 | ||||||
chr7:55824209
|
G | A | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.721-4986C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824209 | ||||||
chr7:55824244
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.721-5021A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824244 | ||||||
chr7:55824295
|
A | C | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-5072T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824295 | ||||||
chr7:55824580
|
C | G | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.721-5357G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824580 | ||||||
chr7:55824586
|
T | C | 278 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(275): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.721-5363A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824586 | ||||||
chr7:55824607
|
A | T | 36 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(33): Show | 36 | HG01123.hp2 HG01243.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.721-5384T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824607 | ||||||
chr7:55824610
|
C | T | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-5387G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824610 | ||||||
chr7:55824628
|
C | CA | 213 | a0001c0001t0001g0077a0001c0001t0001g0229a0001c0001t0001g0242others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.721-5406dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824628 | ||||||
chr7:55824628
|
C | CAA | 127 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0250others(124): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.721-5407_721-5406d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824628 | ||||||
chr7:55824703
|
C | T | 36 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(33): Show | 36 | HG01123.hp2 HG01243.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.721-5480G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824703 | ||||||
chr7:55824807
|
A | AT | 73 | a0001c0001t0001g0242a0001c0001t0001g0331a0001c0001t0002g0014others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.721-5585dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824807 | ||||||
chr7:55824915
|
AGTAACCA others(4): Show |
A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-5703_721-5693d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824915 | ||||||
chr7:55824937
|
T | A | 1 | a0001c0001t0005g0138 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.721-5714A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55824937 | ||||||
chr7:55825023
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-5800C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825023 | ||||||
chr7:55825054
|
T | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-5831A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825054 | ||||||
chr7:55825235
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.721-6012C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825235 | ||||||
chr7:55825301
|
G | A | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-6078C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825301 | ||||||
chr7:55825377
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-6154A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825377 | ||||||
chr7:55825417
|
T | C | 2 | a0001c0001t0005g0327a0001c0001t0033g0251 | 2 | HG01168.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.721-6194A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825417 | ||||||
chr7:55825449
|
C | T | 2 | a0002c0002t0011g0009a0002c0002t0011g0010 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.721-6226G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825449 | ||||||
chr7:55825689
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.721-6466C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825689 | ||||||
chr7:55825737
|
C | A | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-6514G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825737 | ||||||
chr7:55825782
|
C | T | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-6559G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825782 | ||||||
chr7:55825884
|
C | T | 36 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(33): Show | 36 | HG01123.hp2 HG01243.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.721-6661G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825884 | ||||||
chr7:55825929
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-6706G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825929 | ||||||
chr7:55825937
|
A | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-6714T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825937 | ||||||
chr7:55825960
|
G | A | 1 | a0001c0001t0015g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.721-6737C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55825960 | ||||||
chr7:55826017
|
G | A | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-6794C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826017 | ||||||
chr7:55826018
|
C | T | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-6795G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826018 | ||||||
chr7:55826033
|
C | T | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.721-6810G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826033 | ||||||
chr7:55826051
|
G | A | 7 | a0001c0001t0004g0124a0001c0001t0004g0135a0001c0001t0004g0139others(4): Show | 7 | HG01123.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-6828C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826051 | ||||||
chr7:55826057
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.721-6834C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826057 | ||||||
chr7:55826057
|
G | GAGCCACT others(2820): Show |
1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-6835_721-6834i others(2829): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826057 | ||||||
chr7:55826352
|
A | G | 1 | a0001c0001t0006g0367 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.721-7129T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826352 | ||||||
chr7:55826380
|
G | A | 2 | a0001c0001t0005g0112a0001c0001t0005g0115 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.721-7157C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826380 | ||||||
chr7:55826380
|
G | T | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-7157C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826380 | ||||||
chr7:55826435
|
T | C | 1 | a0010c0007t0009g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.721-7212A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826435 | ||||||
chr7:55826535
|
C | T | 1 | a0001c0001t0005g0200 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.721-7312G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826535 | ||||||
chr7:55826626
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721-7403A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826626 | ||||||
chr7:55826684
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.721-7461G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826684 | ||||||
chr7:55826799
|
G | GA | 147 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0250others(144): Show | 147 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.721-7577dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826799 | ||||||
chr7:55826799
|
GA | G | 66 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.721-7577delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826799 | ||||||
chr7:55826908
|
C | T | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.720+7517G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55826908 | ||||||
chr7:55827255
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.720+7170G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827255 | ||||||
chr7:55827335
|
G | T | 1 | a0001c0001t0005g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.720+7090C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827335 | ||||||
chr7:55827453
|
A | G | 1 | a0001c0001t0025g0388 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+6972T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827453 | ||||||
chr7:55827483
|
C | G | 278 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(275): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.720+6942G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827483 | ||||||
chr7:55827502
|
C | G | 5 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0275others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+6923G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827502 | ||||||
chr7:55827543
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+6882G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827543 | ||||||
chr7:55827574
|
C | T | 2 | a0001c0001t0004g0127a0001c0001t0004g0132 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.720+6851G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827574 | ||||||
chr7:55827596
|
C | G | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.720+6829G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827596 | ||||||
chr7:55827778
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+6647G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55827778 | ||||||
chr7:55828004
|
T | TAAGAAGT others(2242): Show |
1 | a0001c0001t0018g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.720+6420_720+6421i others(2251): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828004 | ||||||
chr7:55828128
|
T | C | 1 | a0001c0001t0023g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.720+6297A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828128 | ||||||
chr7:55828299
|
C | CT | 146 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0242others(143): Show | 146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.720+6125dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828299 | ||||||
chr7:55828299
|
C | CTT | 7 | a0001c0001t0001g0273a0001c0001t0001g0310a0001c0001t0001g0323others(4): Show | 7 | HG01433.hp1 HG01952.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+6124_720+6125d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828299 | ||||||
chr7:55828299
|
CT | C | 31 | a0001c0001t0001g0229a0001c0001t0002g0147a0001c0001t0002g0155others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.720+6125delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828299 | ||||||
chr7:55828317
|
C | T | 1 | a0001c0001t0006g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.720+6108G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828317 | ||||||
chr7:55828605
|
G | A | 1 | a0001c0001t0023g0195 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.720+5820C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828605 | ||||||
chr7:55828650
|
A | C | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+5775T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828650 | ||||||
chr7:55828702
|
C | T | 5 | a0001c0001t0002g0152a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+5723G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828702 | ||||||
chr7:55828718
|
A | G | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720+5707T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828718 | ||||||
chr7:55828850
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+5575C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828850 | ||||||
chr7:55828851
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.720+5574C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55828851 | ||||||
chr7:55829004
|
ATTAT | A | 38 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0185others(35): Show | 38 | HG00597.hp2 HG02015.hp2 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.720+5417_720+5420d others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829004 | ||||||
chr7:55829085
|
G | C | 1 | a0001c0001t0001g0353 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.720+5340C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829085 | ||||||
chr7:55829156
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+5269T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829156 | ||||||
chr7:55829274
|
G | A | 1 | a0001c0001t0005g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.720+5151C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829274 | ||||||
chr7:55829334
|
G | A | 2 | a0001c0001t0024g0298a0001c0001t0024g0352 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.720+5091C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829334 | ||||||
chr7:55829378
|
C | CA | 71 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.720+5046dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829378 | ||||||
chr7:55829378
|
CA | C | 16 | a0001c0001t0003g0035a0001c0001t0003g0071a0001c0001t0004g0377others(13): Show | 16 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.720+5046delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829378 | ||||||
chr7:55829422
|
T | C | 13 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0079others(10): Show | 13 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.720+5003A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829422 | ||||||
chr7:55829511
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+4914G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829511 | ||||||
chr7:55829631
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+4794A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829631 | ||||||
chr7:55829661
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+4764G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829661 | ||||||
chr7:55829690
|
ACAGCTCT others(82): Show |
A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | NA18970.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4646_720+4734d others(91): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829690 | ||||||
chr7:55829820
|
C | CA | 135 | a0001c0001t0001g0242a0001c0001t0001g0267a0001c0001t0001g0275others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.720+4604dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829820
|
C | CAA | 64 | a0001c0001t0001g0229a0001c0001t0001g0266a0001c0001t0001g0272others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.720+4603_720+4604d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829820
|
C | CAAA | 77 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(74): Show | 77 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.720+4602_720+4604d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829820
|
C | CAAAA | 15 | a0001c0001t0001g0237a0001c0001t0001g0273a0001c0001t0001g0276others(12): Show | 15 | HG01106.hp1 HG02135.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+4601_720+4604d others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829820
|
C | CAAAAA | 6 | a0001c0001t0001g0274a0001c0001t0001g0296a0001c0001t0001g0300others(3): Show | 6 | HG01123.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4600_720+4604d others(7): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829820
|
CA | C | 15 | a0001c0001t0003g0037a0001c0001t0004g0129a0001c0001t0004g0377others(12): Show | 15 | HG01256.hp2 HG01257.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4604delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829820 | ||||||
chr7:55829994
|
C | T | 1 | a0001c0001t0003g0027 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.720+4431G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55829994 | ||||||
chr7:55830005
|
C | G | 1 | a0001c0001t0008g0046 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.720+4420G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830005 | ||||||
chr7:55830033
|
C | T | 5 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0343others(2): Show | 5 | NA18947.hp1 NA18990.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+4392G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830033 | ||||||
chr7:55830038
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+4387G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830038 | ||||||
chr7:55830048
|
G | A | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.720+4377C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830048 | ||||||
chr7:55830063
|
A | C | 32 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(29): Show | 32 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.720+4362T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830063 | ||||||
chr7:55830126
|
A | G | 71 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.720+4299T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830126 | ||||||
chr7:55830156
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4269G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830156 | ||||||
chr7:55830177
|
C | CA | 38 | a0001c0001t0001g0077a0001c0001t0001g0323a0001c0001t0002g0188others(35): Show | 38 | HG00544.hp2 HG01243.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.720+4247dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830177 | ||||||
chr7:55830194
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4231G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830194 | ||||||
chr7:55830195
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4230A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830195 | ||||||
chr7:55830202
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4223A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830202 | ||||||
chr7:55830204
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4221A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830204 | ||||||
chr7:55830207
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4218A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830207 | ||||||
chr7:55830209
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4216G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830209 | ||||||
chr7:55830211
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4214A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830211 | ||||||
chr7:55830216
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4209G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830216 | ||||||
chr7:55830217
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4208G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830217 | ||||||
chr7:55830219
|
A | T | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4206T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830219 | ||||||
chr7:55830220
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4205G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830220 | ||||||
chr7:55830221
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4204A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830221 | ||||||
chr7:55830230
|
A | T | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4195T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830230 | ||||||
chr7:55830231
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4194G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830231 | ||||||
chr7:55830243
|
A | C | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4182T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830243 | ||||||
chr7:55830244
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4181A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830244 | ||||||
chr7:55830245
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4180G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830245 | ||||||
chr7:55830246
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4179A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830246 | ||||||
chr7:55830247
|
T | G | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4178A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830247 | ||||||
chr7:55830267
|
G | C | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4158C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830267 | ||||||
chr7:55830269
|
T | G | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4156A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830269 | ||||||
chr7:55830270
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.720+4155G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830270 | ||||||
chr7:55830283
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.720+4142C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830283 | ||||||
chr7:55830321
|
GTA | G | 12 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0381others(9): Show | 12 | HG00544.hp2 HG00639.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+4102_720+4103d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830321 | ||||||
chr7:55830321
|
GTATA | G | 12 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0382others(9): Show | 12 | HG01256.hp2 HG01261.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+4100_720+4103d others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830321 | ||||||
chr7:55830321
|
GTATATAT others(3): Show |
G | 7 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(4): Show | 7 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+4094_720+4103d others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830321 | ||||||
chr7:55830323
|
A | G | 1 | a0002c0002t0003g0007 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.720+4102T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830323 | ||||||
chr7:55830329
|
A | G | 1 | a0001c0011t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.720+4096T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830329 | ||||||
chr7:55830336
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+4078_720+4088d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830336 | ||||||
chr7:55830338
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+4087A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830338 | ||||||
chr7:55830338
|
TATATATA others(4): Show |
T | 15 | a0001c0001t0001g0252a0001c0001t0001g0257a0001c0001t0001g0272others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4076_720+4086d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830338 | ||||||
chr7:55830339
|
ATATATAT others(4): Show |
A | 69 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0256others(66): Show | 69 | HG00621.hp2 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.720+4075_720+4085d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830339 | ||||||
chr7:55830339
|
ATATATAT others(5): Show |
A | 9 | a0001c0001t0001g0013a0001c0001t0001g0294a0001c0001t0001g0329others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+4074_720+4085d others(14): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830339 | ||||||
chr7:55830340
|
TATA | T | 4 | a0001c0001t0001g0237a0001c0001t0005g0186a0001c0001t0005g0196others(1): Show | 4 | HG00609.hp2 HG02602.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4082_720+4084d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830340 | ||||||
chr7:55830341
|
A | T | 1 | a0001c0001t0005g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.720+4084T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830341 | ||||||
chr7:55830341
|
ATATATAT others(3): Show |
A | 11 | a0001c0001t0001g0279a0001c0001t0001g0311a0001c0001t0001g0312others(8): Show | 11 | HG00408.hp1 HG01981.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+4074_720+4083d others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830341 | ||||||
chr7:55830341
|
ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0278a0001c0001t0001g0285a0001c0001t0001g0295others(4): Show | 7 | HG02135.hp2 HG02717.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+4073_720+4083d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830341 | ||||||
chr7:55830342
|
TATA | T | 13 | a0001c0001t0001g0229a0001c0001t0005g0197a0001c0001t0005g0198others(10): Show | 13 | HG01099.hp2 HG01109.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+4080_720+4082d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830342 | ||||||
chr7:55830343
|
A | T | 8 | a0001c0001t0002g0184a0001c0001t0004g0117a0001c0001t0005g0187others(5): Show | 8 | HG00597.hp1 HG01175.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+4082T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830343 | ||||||
chr7:55830344
|
TA | T | 7 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0035others(4): Show | 7 | HG00280.hp1 HG01106.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+4080delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830344 | ||||||
chr7:55830345
|
A | AT | 5 | a0001c0001t0003g0036a0001c0001t0004g0305a0001c0001t0004g0306others(2): Show | 5 | HG02683.hp2 HG06807.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+4079dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830345 | ||||||
chr7:55830345
|
A | ATTT | 23 | a0001c0001t0002g0147a0001c0001t0002g0149a0001c0001t0002g0152others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.720+4079_720+4080i others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830345 | ||||||
chr7:55830345
|
A | ATTTT | 4 | a0001c0001t0001g0242a0001c0001t0002g0175a0001c0001t0002g0218others(1): Show | 4 | HG01515.hp1 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+4079_720+4080i others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830345 | ||||||
chr7:55830345
|
A | T | 26 | a0001c0001t0001g0237a0001c0001t0002g0184a0001c0001t0003g0052others(23): Show | 26 | HG00597.hp1 HG00609.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.720+4080T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830345 | ||||||
chr7:55830346
|
TA | T | 14 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0032others(11): Show | 14 | HG00099.hp2 HG01081.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+4078delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830346 | ||||||
chr7:55830346
|
TATA | T | 3 | a0002c0002t0003g0007a0002c0002t0011g0009a0002c0002t0011g0010 | 3 | HG01123.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.720+4076_720+4078d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830346 | ||||||
chr7:55830347
|
A | ATT | 6 | a0001c0001t0004g0127a0001c0001t0004g0132a0001c0001t0004g0140others(3): Show | 6 | HG00140.hp2 HG02080.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4077_720+4078i others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | ATTTT | 4 | a0001c0001t0002g0171a0001c0001t0003g0044a0001c0001t0003g0054others(1): Show | 4 | NA18969.hp1 NA18987.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4077_720+4078i others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | ATTTTT | 8 | a0001c0001t0002g0014a0001c0001t0002g0201a0001c0001t0002g0206others(5): Show | 8 | HG01261.hp2 HG02083.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+4077_720+4078i others(7): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0017g0092a0001c0001t0017g0093a0001c0001t0017g0094 | 3 | HG02615.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.720+4077_720+4078i others(19): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0017g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+4077_720+4078i others(20): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0006g0074a0001c0001t0006g0145 | 2 | HG01993.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.720+4077_720+4078i others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830347
|
A | T | 95 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0242others(92): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.720+4078T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830347 | ||||||
chr7:55830349
|
A | AT | 7 | a0001c0001t0003g0034a0001c0001t0003g0040a0001c0001t0003g0047others(4): Show | 7 | HG01074.hp2 HG01928.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+4075dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(42): Show |
1 | a0001c0001t0030g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(51): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0038g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(43): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0006g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(46): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0027g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(41): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0006g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(42): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0027g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(32): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0006g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(41): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0007g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(20): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(16): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0035g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(37): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0006g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(26): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0006g0073a0001c0001t0006g0081 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.720+4075_720+4076i others(26): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(3): Show |
1 | a0001c0001t0034g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(14): Show |
1 | a0001c0001t0006g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(23): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(15): Show |
1 | a0001c0001t0006g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(24): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(16): Show |
1 | a0007c0008t0006g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(25): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(17): Show |
1 | a0001c0001t0006g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(26): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATATTT others(19): Show |
1 | a0001c0001t0001g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(28): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0002g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0006g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(17): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATTTTT others(12): Show |
2 | a0001c0001t0006g0090a0001c0001t0006g0099 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.720+4075_720+4076i others(21): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATTTTT others(13): Show |
1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATATTTTT others(14): Show |
2 | a0001c0001t0006g0079a0001c0001t0006g0091 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+4075_720+4076i others(23): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATTTTT | 16 | a0001c0001t0002g0191a0001c0001t0002g0210a0001c0001t0002g0211others(13): Show | 16 | HG00597.hp2 HG03927.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.720+4071_720+4075d others(7): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0006g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(21): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0006g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.720+4075_720+4076i others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATTTTTTT others(14): Show |
1 | a0009c0009t0006g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(23): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0006g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.720+4075_720+4076i others(24): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830349
|
A | T | 152 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0242others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.720+4076T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830349 | ||||||
chr7:55830409
|
C | T | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720+4016G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830409 | ||||||
chr7:55830417
|
G | A | 1 | a0001c0001t0007g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.720+4008C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830417 | ||||||
chr7:55830423
|
T | G | 1 | a0001c0001t0003g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.720+4002A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830423 | ||||||
chr7:55830438
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+3987A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830438 | ||||||
chr7:55830447
|
C | A | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+3978G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830447 | ||||||
chr7:55830559
|
A | G | 1 | a0001c0001t0003g0044 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.720+3866T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830559 | ||||||
chr7:55830638
|
A | C | 147 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.720+3787T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830638 | ||||||
chr7:55830879
|
T | G | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.720+3546A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830879 | ||||||
chr7:55830890
|
A | G | 3 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.720+3535T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830890 | ||||||
chr7:55830942
|
AT | A | 4 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+3482delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55830942 | ||||||
chr7:55831074
|
A | T | 5 | a0001c0001t0002g0152a0001c0001t0002g0162a0001c0001t0002g0163others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+3351T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831074 | ||||||
chr7:55831091
|
C | T | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.720+3334G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831091 | ||||||
chr7:55831124
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+3301C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831124 | ||||||
chr7:55831149
|
C | A | 1 | a0001c0001t0002g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.720+3276G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831149 | ||||||
chr7:55831256
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.720+3169A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831256 | ||||||
chr7:55831308
|
A | G | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.720+3117T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831308 | ||||||
chr7:55831351
|
G | A | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+3074C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831351 | ||||||
chr7:55831378
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+3047T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831378 | ||||||
chr7:55831481
|
G | A | 120 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(117): Show | 120 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.720+2944C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831481 | ||||||
chr7:55831520
|
TC | T | 3 | a0001c0001t0029g0026a0005c0004t0003g0049a0005c0004t0003g0070 | 3 | HG00099.hp2 HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.720+2904delG | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831520 | ||||||
chr7:55831803
|
T | C | 341 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.720+2622A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831803 | ||||||
chr7:55831913
|
C | A | 1 | a0001c0001t0028g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.720+2512G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831913 | ||||||
chr7:55831927
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.720+2498G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55831927 | ||||||
chr7:55832095
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+2330C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832095 | ||||||
chr7:55832120
|
G | A | 1 | a0001c0001t0016g0192 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.720+2305C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832120 | ||||||
chr7:55832202
|
A | AAC | 3 | a0001c0001t0005g0111a0002c0002t0011g0009a0002c0002t0011g0010 | 3 | HG01978.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.720+2221_720+2222d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AAC | A | 52 | a0001c0001t0001g0237a0001c0001t0001g0250a0001c0001t0001g0258others(49): Show | 52 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.720+2221_720+2222d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AACAC | A | 145 | a0001c0001t0001g0013a0001c0001t0001g0252a0001c0001t0001g0254others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.720+2219_720+2222d others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AACACAC | A | 52 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0173others(49): Show | 52 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(49): Show |
intron_variant | MODIFIER | c.720+2217_720+2222d others(8): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AACACACA others(1): Show |
A | 106 | a0001c0001t0001g0077a0001c0001t0002g0021a0001c0001t0002g0030others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.720+2215_720+2222d others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AACACACA others(3): Show |
A | 6 | a0001c0001t0001g0317a0001c0001t0006g0073a0001c0001t0006g0081others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+2213_720+2222d others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832202
|
AACACACA others(7): Show |
A | 5 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(2): Show | 5 | HG03041.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+2209_720+2222d others(16): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832202 | ||||||
chr7:55832246
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+2179T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832246 | ||||||
chr7:55832349
|
A | G | 4 | a0001c0001t0011g0376a0001c0001t0015g0260a0001c0001t0032g0356others(1): Show | 4 | HG03041.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2076T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832349 | ||||||
chr7:55832379
|
C | T | 1 | a0001c0001t0032g0356 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+2046G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832379 | ||||||
chr7:55832387
|
C | T | 3 | a0001c0001t0010g0378a0004c0005t0010g0157a0004c0005t0010g0158 | 3 | HG01256.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.720+2038G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832387 | ||||||
chr7:55832541
|
GTATATAT others(16): Show |
G | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.720+1861_720+1883d others(25): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832541 | ||||||
chr7:55832621
|
C | T | 1 | a0001c0006t0005g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+1804G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832621 | ||||||
chr7:55832628
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+1797G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832628 | ||||||
chr7:55832770
|
G | A | 2 | a0001c0001t0005g0112a0001c0001t0005g0115 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.720+1655C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832770 | ||||||
chr7:55832803
|
T | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+1622A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55832803 | ||||||
chr7:55833048
|
C | G | 1 | a0001c0001t0002g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.720+1377G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833048 | ||||||
chr7:55833113
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.720+1312C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833113 | ||||||
chr7:55833162
|
C | A | 147 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.720+1263G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833162 | ||||||
chr7:55833171
|
C | T | 1 | a0001c0001t0018g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.720+1254G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833171 | ||||||
chr7:55833183
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.720+1242G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833183 | ||||||
chr7:55833184
|
G | A | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.720+1241C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833184 | ||||||
chr7:55833195
|
G | T | 1 | a0001c0001t0009g0363 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.720+1230C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833195 | ||||||
chr7:55833261
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+1164C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833261 | ||||||
chr7:55833301
|
A | G | 147 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.720+1124T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833301 | ||||||
chr7:55833309
|
C | A | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+1116G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833309 | ||||||
chr7:55833314
|
C | CA | 8 | a0001c0001t0006g0079a0001c0001t0006g0091a0001c0001t0006g0095others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+1110dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833314 | ||||||
chr7:55833394
|
TAAC | T | 4 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0001g0337others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1028_720+1030d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833394 | ||||||
chr7:55833457
|
C | T | 1 | a0001c0001t0010g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720+968G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833457 | ||||||
chr7:55833458
|
G | A | 3 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0015g0086 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.720+967C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833458 | ||||||
chr7:55833525
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+900A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833525 | ||||||
chr7:55833754
|
A | T | 153 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0250others(150): Show | 153 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.720+671T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833754 | ||||||
chr7:55833761
|
G | GA | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.720+663dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833761 | ||||||
chr7:55833775
|
A | T | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.720+650T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833775 | ||||||
chr7:55833776
|
T | C | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.720+649A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833776 | ||||||
chr7:55833777
|
C | A | 1 | a0001c0001t0002g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.720+648G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55833777 | ||||||
chr7:55834001
|
T | C | 1 | a0010c0007t0009g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.720+424A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834001 | ||||||
chr7:55834020
|
A | G | 4 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0009others(1): Show | 4 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+405T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834020 | ||||||
chr7:55834022
|
T | C | 1 | a0001c0001t0009g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.720+403A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834022 | ||||||
chr7:55834040
|
A | C | 1 | a0001c0001t0002g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.720+385T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834040 | ||||||
chr7:55834160
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.720+265C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834160 | ||||||
chr7:55834303
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+122A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834303 | ||||||
chr7:55834335
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.720+90T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834335 | ||||||
chr7:55834351
|
T | A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.720+74A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 6/9 | chr7 | 55834351 | ||||||
chr7:55834649
|
G | C | 1 | a0001c0001t0006g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.559-63C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834649 | ||||||
chr7:55834692
|
G | C | 4 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0009others(1): Show | 4 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-106C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834692 | ||||||
chr7:55834693
|
A | T | 2 | a0001c0001t0012g0270a0001c0001t0012g0302 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.559-107T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834693 | ||||||
chr7:55834700
|
G | C | 4 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0009others(1): Show | 4 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-114C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834700 | ||||||
chr7:55834701
|
G | A | 4 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0009others(1): Show | 4 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-115C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834701 | ||||||
chr7:55834705
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0329 | 2 | NA18945.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.559-119G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834705 | ||||||
chr7:55834706
|
G | A | 1 | a0001c0001t0001g0342 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.559-120C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834706 | ||||||
chr7:55834748
|
C | T | 3 | a0001c0001t0017g0078a0001c0001t0017g0092a0001c0001t0017g0093 | 3 | HG02615.hp1 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.559-162G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834748 | ||||||
chr7:55834784
|
A | C | 1 | a0001c0001t0007g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.559-198T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55834784 | ||||||
chr7:55835036
|
T | A | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.559-450A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835036 | ||||||
chr7:55835185
|
T | TTTTA | 18 | a0001c0001t0001g0355a0001c0001t0002g0165a0001c0001t0002g0173others(15): Show | 18 | HG00673.hp2 HG01123.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.559-603_559-600dup others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835185 | ||||||
chr7:55835185
|
T | TTTTATTT others(13): Show |
1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-619_559-600dup others(20): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835185 | ||||||
chr7:55835231
|
G | C | 343 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.559-645C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835231 | ||||||
chr7:55835235
|
C | T | 1 | a0002c0002t0003g0007 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.559-649G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835235 | ||||||
chr7:55835271
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-685A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835271 | ||||||
chr7:55835301
|
C | G | 1 | a0001c0001t0005g0200 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.559-715G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835301 | ||||||
chr7:55835393
|
G | A | 1 | a0001c0001t0015g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.559-807C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835393 | ||||||
chr7:55835449
|
G | A | 60 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.559-863C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835449 | ||||||
chr7:55835693
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.559-1107G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835693 | ||||||
chr7:55835804
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-1218C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835804 | ||||||
chr7:55835891
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.559-1305G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55835891 | ||||||
chr7:55836340
|
T | C | 1 | a0002c0002t0003g0007 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.559-1754A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836340 | ||||||
chr7:55836346
|
C | T | 107 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(104): Show | 107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.559-1760G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836346 | ||||||
chr7:55836465
|
G | C | 1 | a0001c0001t0001g0341 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.559-1879C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836465 | ||||||
chr7:55836476
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.559-1890G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836476 | ||||||
chr7:55836558
|
A | G | 341 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.559-1972T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836558 | ||||||
chr7:55836568
|
G | A | 120 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(117): Show | 120 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.559-1982C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836568 | ||||||
chr7:55836734
|
G | A | 9 | a0001c0001t0001g0279a0001c0001t0001g0311a0001c0001t0001g0314others(6): Show | 9 | HG01981.hp1 HG02015.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.559-2148C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836734 | ||||||
chr7:55836737
|
T | TCAA | 61 | a0001c0001t0001g0250a0001c0001t0002g0021a0001c0001t0002g0030others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.559-2154_559-2152d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836737 | ||||||
chr7:55836890
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-2304C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836890 | ||||||
chr7:55836992
|
AAGTTGAA others(139): Show |
A | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559-2552_559-2407d others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836992 | ||||||
chr7:55836993
|
A | G | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.559-2407T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836993 | ||||||
chr7:55836999
|
A | G | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.559-2413T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55836999 | ||||||
chr7:55837034
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-2448C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837034 | ||||||
chr7:55837109
|
C | CT | 63 | a0001c0001t0001g0273a0001c0001t0001g0341a0001c0001t0002g0021others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.559-2524dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837109 | ||||||
chr7:55837123
|
TGAG | T | 3 | a0003c0003t0019g0002a0003c0003t0019g0003a0003c0003t0019g0004 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-2540_559-2538d others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837123 | ||||||
chr7:55837124
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.559-2538C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837124 | ||||||
chr7:55837125
|
A | T | 1 | a0001c0001t0002g0160 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.559-2539T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837125 | ||||||
chr7:55837127
|
A | T | 3 | a0003c0003t0019g0002a0003c0003t0019g0003a0003c0003t0019g0004 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-2541T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837127 | ||||||
chr7:55837140
|
G | A | 1 | a0001c0001t0004g0384 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.559-2554C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837140 | ||||||
chr7:55837263
|
G | A | 341 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.559-2677C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837263 | ||||||
chr7:55837575
|
T | C | 2 | a0001c0001t0005g0241a0001c0001t0005g0247 | 2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.559-2989A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837575 | ||||||
chr7:55837661
|
G | A | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.559-3075C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837661 | ||||||
chr7:55837708
|
G | A | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.559-3122C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837708 | ||||||
chr7:55837738
|
A | G | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.559-3152T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837738 | ||||||
chr7:55837832
|
C | G | 2 | a0001c0001t0003g0052a0001c0001t0003g0071 | 2 | NA19003.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.559-3246G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837832 | ||||||
chr7:55837891
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-3305A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55837891 | ||||||
chr7:55838129
|
G | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0168 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.559-3543C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838129 | ||||||
chr7:55838132
|
CAG | C | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.559-3548_559-3547d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838132 | ||||||
chr7:55838141
|
A | C | 26 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0002g0234others(23): Show | 26 | HG00609.hp2 HG00639.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.559-3555T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838141 | ||||||
chr7:55838203
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.559-3617G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838203 | ||||||
chr7:55838437
|
CCA | C | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-3853_559-3852d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838437 | ||||||
chr7:55838453
|
T | C | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-3867A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838453 | ||||||
chr7:55838481
|
C | T | 26 | a0001c0001t0002g0147a0001c0001t0002g0149a0001c0001t0002g0152others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.559-3895G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838481 | ||||||
chr7:55838523
|
T | TC | 32 | a0001c0001t0001g0262a0001c0001t0001g0280a0001c0001t0001g0288others(29): Show | 32 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.559-3938dupG | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838523 | ||||||
chr7:55838545
|
C | T | 4 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0146others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-3959G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838545 | ||||||
chr7:55838705
|
G | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.559-4119C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838705 | ||||||
chr7:55838715
|
T | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559-4129A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838715 | ||||||
chr7:55838751
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.559-4165T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838751 | ||||||
chr7:55838860
|
T | C | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.558+4082A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55838860 | ||||||
chr7:55839020
|
T | G | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.558+3922A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839020 | ||||||
chr7:55839076
|
G | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.558+3866C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839076 | ||||||
chr7:55839092
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.558+3850T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839092 | ||||||
chr7:55839157
|
G | T | 35 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(32): Show | 35 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.558+3785C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839157 | ||||||
chr7:55839215
|
C | T | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.558+3727G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839215 | ||||||
chr7:55839237
|
A | T | 7 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(4): Show | 7 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.558+3705T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839237 | ||||||
chr7:55839391
|
G | GA | 64 | a0001c0001t0001g0256a0001c0001t0001g0355a0001c0001t0002g0021others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.558+3550dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839391 | ||||||
chr7:55839391
|
GA | G | 25 | a0001c0001t0001g0343a0001c0001t0002g0179a0001c0001t0002g0205others(22): Show | 25 | HG00544.hp2 HG00673.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.558+3550delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839391 | ||||||
chr7:55839574
|
A | G | 70 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.558+3368T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55839574 | ||||||
chr7:55840126
|
T | TA | 7 | a0001c0001t0002g0248a0001c0001t0003g0035a0001c0001t0003g0036others(4): Show | 7 | HG02257.hp1 HG03516.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.558+2815dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840126 | ||||||
chr7:55840126
|
TA | T | 12 | a0001c0001t0001g0318a0001c0001t0001g0333a0001c0001t0002g0162others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+2815delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840126 | ||||||
chr7:55840212
|
G | A | 1 | a0001c0001t0006g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.558+2730C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840212 | ||||||
chr7:55840299
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.558+2643C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840299 | ||||||
chr7:55840305
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.558+2637T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840305 | ||||||
chr7:55840347
|
G | A | 1 | a0001c0001t0008g0046 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.558+2595C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840347 | ||||||
chr7:55840394
|
T | C | 2 | a0001c0001t0006g0083a0001c0001t0006g0097 | 2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.558+2548A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840394 | ||||||
chr7:55840518
|
C | A | 147 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.558+2424G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840518 | ||||||
chr7:55840575
|
G | C | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.558+2367C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840575 | ||||||
chr7:55840617
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.558+2325G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840617 | ||||||
chr7:55840697
|
A | C | 149 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.558+2245T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840697 | ||||||
chr7:55840888
|
GTTATTAT others(4): Show |
G | 70 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.558+2043_558+2053d others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840888 | ||||||
chr7:55840960
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.558+1982G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55840960 | ||||||
chr7:55841003
|
G | A | 10 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0275others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+1939C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841003 | ||||||
chr7:55841151
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+1791A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841151 | ||||||
chr7:55841199
|
G | A | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+1743C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841199 | ||||||
chr7:55841224
|
T | A | 1 | a0001c0001t0005g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.558+1718A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841224 | ||||||
chr7:55841228
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+1714C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841228 | ||||||
chr7:55841258
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+1684C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841258 | ||||||
chr7:55841342
|
T | C | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.558+1600A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841342 | ||||||
chr7:55841578
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.558+1364C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841578 | ||||||
chr7:55841701
|
C | T | 35 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(32): Show | 35 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.558+1241G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841701 | ||||||
chr7:55841802
|
C | T | 1 | a0001c0006t0005g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.558+1140G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841802 | ||||||
chr7:55841812
|
G | A | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.558+1130C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841812 | ||||||
chr7:55841853
|
C | CA | 70 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0250others(67): Show | 70 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.558+1088dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841853 | ||||||
chr7:55841853
|
C | CAA | 7 | a0001c0001t0001g0319a0001c0001t0001g0342a0001c0001t0005g0199others(4): Show | 7 | HG01109.hp2 HG01255.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.558+1087_558+1088d others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841853 | ||||||
chr7:55841853
|
CA | C | 12 | a0001c0001t0001g0262a0001c0001t0001g0273a0001c0001t0001g0274others(9): Show | 12 | HG00621.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+1088delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841853 | ||||||
chr7:55841901
|
C | A | 1 | a0001c0001t0016g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.558+1041G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841901 | ||||||
chr7:55841926
|
T | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+1016A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841926 | ||||||
chr7:55841927
|
T | A | 1 | a0001c0001t0005g0221 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.558+1015A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841927 | ||||||
chr7:55841938
|
G | A | 1 | a0001c0001t0003g0045 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.558+1004C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841938 | ||||||
chr7:55841960
|
A | G | 147 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.558+982T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55841960 | ||||||
chr7:55842170
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.558+772C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842170 | ||||||
chr7:55842269
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+673C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842269 | ||||||
chr7:55842558
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.558+384T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842558 | ||||||
chr7:55842567
|
C | A | 4 | a0001c0001t0006g0073a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+375G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842567 | ||||||
chr7:55842608
|
CA | C | 120 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(117): Show | 120 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.558+333delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842608 | ||||||
chr7:55842616
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.558+326T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842616 | ||||||
chr7:55842641
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.558+301C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842641 | ||||||
chr7:55842774
|
G | A | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.558+168C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842774 | ||||||
chr7:55842854
|
G | A | 5 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0008g0046others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+88C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842854 | ||||||
chr7:55842863
|
G | A | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+79C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842863 | ||||||
chr7:55842907
|
CA | C | 7 | a0001c0001t0001g0333a0001c0001t0006g0087a0001c0001t0006g0089others(4): Show | 7 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.558+34delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 5/9 | chr7 | 55842907 | ||||||
chr7:55843203
|
A | C | 1 | a0001c0001t0001g0301 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.372-75T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843203 | ||||||
chr7:55843310
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.372-182A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843310 | ||||||
chr7:55843338
|
G | A | 1 | a0001c0001t0006g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.372-210C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843338 | ||||||
chr7:55843394
|
C | G | 1 | a0001c0001t0001g0294 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.372-266G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843394 | ||||||
chr7:55843572
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372-444C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843572 | ||||||
chr7:55843618
|
G | C | 70 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.372-490C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843618 | ||||||
chr7:55843789
|
G | A | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-661C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843789 | ||||||
chr7:55843797
|
G | A | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-669C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843797 | ||||||
chr7:55843986
|
A | G | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.371+537T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55843986 | ||||||
chr7:55844030
|
A | G | 3 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145 | 3 | HG02257.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.371+493T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844030 | ||||||
chr7:55844126
|
A | G | 1 | a0001c0001t0010g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.371+397T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844126 | ||||||
chr7:55844249
|
T | C | 1 | a0001c0001t0006g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.371+274A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844249 | ||||||
chr7:55844305
|
C | T | 1 | a0001c0001t0018g0358 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.371+218G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844305 | ||||||
chr7:55844457
|
T | C | 1 | a0001c0001t0001g0360 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.371+66A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844457 | ||||||
chr7:55844492
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.371+31G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 4/9 | chr7 | 55844492 | ||||||
chr7:55844912
|
C | CT | 312 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0242others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.176-195dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55844912 | ||||||
chr7:55844965
|
G | A | 342 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(339): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.176-247C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55844965 | ||||||
chr7:55845171
|
A | G | 2 | a0001c0001t0015g0085a0001c0001t0015g0086 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.176-453T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845171 | ||||||
chr7:55845263
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.176-545G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845263 | ||||||
chr7:55845271
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.176-553G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845271 | ||||||
chr7:55845272
|
G | A | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-554C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845272 | ||||||
chr7:55845324
|
G | C | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-606C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845324 | ||||||
chr7:55845332
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.176-614T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845332 | ||||||
chr7:55845342
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.176-624A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845342 | ||||||
chr7:55845427
|
C | T | 26 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0002g0234others(23): Show | 26 | HG00609.hp2 HG00639.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.176-709G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845427 | ||||||
chr7:55845508
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.176-790A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845508 | ||||||
chr7:55845581
|
G | A | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-863C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845581 | ||||||
chr7:55845756
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+761T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845756 | ||||||
chr7:55845771
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+746G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845771 | ||||||
chr7:55845788
|
G | A | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+729C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845788 | ||||||
chr7:55845821
|
G | A | 1 | a0001c0001t0021g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+696C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845821 | ||||||
chr7:55845958
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.175+559T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845958 | ||||||
chr7:55845973
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+544A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845973 | ||||||
chr7:55845974
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+543C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845974 | ||||||
chr7:55845980
|
C | T | 5 | a0001c0001t0004g0304a0001c0001t0004g0305a0001c0001t0004g0306others(2): Show | 5 | HG00733.hp2 HG01255.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+537G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845980 | ||||||
chr7:55845998
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+519C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55845998 | ||||||
chr7:55846006
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+511T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846006 | ||||||
chr7:55846022
|
A | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+495T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846022 | ||||||
chr7:55846043
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+474G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846043 | ||||||
chr7:55846050
|
G | A | 144 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.175+467C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846050 | ||||||
chr7:55846064
|
A | AAGTATAT others(4): Show |
2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.175+452_175+453ins others(11): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846064 | ||||||
chr7:55846064
|
A | AAGTATAT others(6): Show |
1 | a0001c0001t0037g0332 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.175+452_175+453ins others(13): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846064 | ||||||
chr7:55846064
|
A | AAGTATAT others(8): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0265 | 2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.175+452_175+453ins others(15): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846064 | ||||||
chr7:55846064
|
A | AAGTATAT others(10): Show |
1 | a0001c0001t0002g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.175+452_175+453ins others(17): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846064 | ||||||
chr7:55846064
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+453T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846064 | ||||||
chr7:55846065
|
G | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0265a0001c0001t0002g0184others(4): Show | 7 | HG00738.hp2 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+452C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTA | 16 | a0001c0001t0003g0025a0001c0001t0003g0034a0001c0001t0003g0064others(13): Show | 16 | HG00280.hp1 HG01109.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.175+450_175+451dup others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATA | 13 | a0001c0001t0001g0267a0001c0001t0003g0020a0001c0001t0003g0027others(10): Show | 13 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+448_175+451dup others(4): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATA | 11 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0001g0285others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+446_175+451dup others(6): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(1): Show |
13 | a0001c0001t0001g0266a0001c0001t0001g0286a0001c0001t0001g0287others(10): Show | 13 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+444_175+451dup others(8): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(3): Show |
8 | a0001c0001t0001g0284a0001c0001t0005g0197a0001c0001t0012g0320others(5): Show | 8 | HG01123.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+442_175+451dup others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(5): Show |
62 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0257others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.175+440_175+451dup others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(7): Show |
57 | a0001c0001t0001g0242a0001c0001t0001g0258a0001c0001t0001g0262others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.175+438_175+451dup others(14): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(9): Show |
50 | a0001c0001t0001g0256a0001c0001t0001g0281a0001c0001t0001g0282others(47): Show | 50 | HG00323.hp1 HG00408.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.175+436_175+451dup others(16): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(11): Show |
53 | a0001c0001t0001g0229a0001c0001t0001g0259a0001c0001t0001g0301others(50): Show | 53 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.175+434_175+451dup others(18): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(13): Show |
11 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0225others(8): Show | 12 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+432_175+451dup others(20): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(15): Show |
8 | a0001c0001t0001g0250a0001c0001t0001g0295a0001c0001t0001g0338others(5): Show | 8 | HG01175.hp1 HG01261.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+430_175+451dup others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0252a0001c0001t0002g0155 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.175+428_175+451dup others(24): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(19): Show |
9 | a0001c0001t0001g0237a0001c0001t0002g0147a0001c0001t0002g0178others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+426_175+451dup others(26): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(21): Show |
4 | a0001c0001t0002g0387a0001c0001t0004g0128a0001c0001t0004g0132others(1): Show | 4 | HG01255.hp2 HG01943.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+451_175+452ins others(28): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0002g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175+451_175+452ins others(30): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0001g0288 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.175+451_175+452ins others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846065
|
GTATATAT others(3): Show |
G | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+442_175+451del others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846065 | ||||||
chr7:55846071
|
ATATATAT others(15): Show |
A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+424_175+445del others(22): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846071 | ||||||
chr7:55846081
|
ATATATAT others(5): Show |
A | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+424_175+435del others(12): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846081 | ||||||
chr7:55846214
|
C | T | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+303G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846214 | ||||||
chr7:55846286
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.175+231G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846286 | ||||||
chr7:55846308
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+209A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 3/9 | chr7 | 55846308 | ||||||
chr7:55846676
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-39T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846676 | ||||||
chr7:55846916
|
G | A | 1 | a0001c0001t0001g0374 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.55-279C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846916 | ||||||
chr7:55846918
|
T | A | 1 | a0001c0006t0005g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-281A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846918 | ||||||
chr7:55846943
|
T | C | 3 | a0003c0003t0019g0002a0003c0003t0019g0003a0003c0003t0019g0004 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.55-306A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846943 | ||||||
chr7:55846959
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-322T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846959 | ||||||
chr7:55846991
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-354C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55846991 | ||||||
chr7:55847022
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-385G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847022 | ||||||
chr7:55847095
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-458A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847095 | ||||||
chr7:55847127
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-490G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847127 | ||||||
chr7:55847228
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-591T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847228 | ||||||
chr7:55847345
|
G | A | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-708C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847345 | ||||||
chr7:55847434
|
T | C | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.55-797A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847434 | ||||||
chr7:55847443
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-806A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847443 | ||||||
chr7:55847512
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-875C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847512 | ||||||
chr7:55847614
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-977G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847614 | ||||||
chr7:55847700
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55-1063T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847700 | ||||||
chr7:55847849
|
A | ACCAACTG others(307): Show |
1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1213_55-1212ins others(314): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847849 | ||||||
chr7:55847902
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1265A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847902 | ||||||
chr7:55847963
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1326G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55847963 | ||||||
chr7:55848030
|
C | T | 7 | a0001c0001t0004g0105a0001c0001t0004g0119a0001c0001t0004g0120others(4): Show | 7 | HG00738.hp1 HG01071.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-1393G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848030 | ||||||
chr7:55848085
|
G | C | 35 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(32): Show | 35 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.55-1448C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848085 | ||||||
chr7:55848124
|
A | C | 1 | a0001c0001t0001g0342 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.55-1487T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848124 | ||||||
chr7:55848148
|
T | A | 1 | a0001c0001t0016g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.55-1511A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848148 | ||||||
chr7:55848231
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1594C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848231 | ||||||
chr7:55848279
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1642C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848279 | ||||||
chr7:55848405
|
G | A | 2 | a0001c0001t0002g0220a0006c0013t0039g0008 | 2 | HG02922.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.55-1768C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848405 | ||||||
chr7:55848505
|
T | C | 343 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(340): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.55-1868A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848505 | ||||||
chr7:55848576
|
T | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1939A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848576 | ||||||
chr7:55848607
|
A | AT | 6 | a0001c0001t0004g0105a0001c0001t0004g0124a0001c0001t0004g0304others(3): Show | 6 | HG00733.hp2 HG00738.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1971dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848607 | ||||||
chr7:55848607
|
AT | A | 223 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0237others(220): Show | 223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.55-1971delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848607 | ||||||
chr7:55848607
|
ATT | A | 42 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.55-1972_55-1971del others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848607 | ||||||
chr7:55848607
|
ATTT | A | 40 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0179others(37): Show | 40 | HG00597.hp2 HG01358.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.55-1973_55-1971del others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848607 | ||||||
chr7:55848621
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1984A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848621 | ||||||
chr7:55848623
|
T | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-1986A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848623 | ||||||
chr7:55848642
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2005C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848642 | ||||||
chr7:55848650
|
G | T | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.55-2013C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848650 | ||||||
chr7:55848674
|
G | A | 10 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(7): Show | 10 | HG00544.hp2 HG01981.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-2037C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848674 | ||||||
chr7:55848701
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55-2064C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848701 | ||||||
chr7:55848733
|
G | A | 2 | a0001c0001t0026g0361a0001c0001t0026g0375 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.55-2096C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848733 | ||||||
chr7:55848764
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2127G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848764 | ||||||
chr7:55848781
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2144C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848781 | ||||||
chr7:55848884
|
G | A | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-2247C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55848884 | ||||||
chr7:55849057
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55-2420C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849057 | ||||||
chr7:55849062
|
C | T | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-2425G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849062 | ||||||
chr7:55849098
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2461T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849098 | ||||||
chr7:55849144
|
G | A | 97 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.55-2507C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849144 | ||||||
chr7:55849154
|
G | A | 5 | a0001c0001t0002g0188a0001c0001t0002g0194a0001c0001t0002g0222others(2): Show | 5 | HG02523.hp2 NA18992.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-2517C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849154 | ||||||
chr7:55849237
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.55-2600T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849237 | ||||||
chr7:55849332
|
A | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2695T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849332 | ||||||
chr7:55849415
|
T | C | 4 | a0001c0001t0006g0075a0001c0001t0006g0083a0001c0001t0006g0097others(1): Show | 4 | HG01433.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-2778A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849415 | ||||||
chr7:55849543
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-2906A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849543 | ||||||
chr7:55849672
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3035C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849672 | ||||||
chr7:55849686
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3049G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849686 | ||||||
chr7:55849737
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3100G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849737 | ||||||
chr7:55849915
|
T | G | 8 | a0001c0001t0001g0266a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-3278A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849915 | ||||||
chr7:55849934
|
T | C | 6 | a0001c0001t0006g0362a0001c0001t0006g0364a0001c0001t0006g0365others(3): Show | 6 | HG02615.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-3297A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55849934 | ||||||
chr7:55850056
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3419T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850056 | ||||||
chr7:55850078
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3441T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850078 | ||||||
chr7:55850132
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3495A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850132 | ||||||
chr7:55850144
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3507T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850144 | ||||||
chr7:55850166
|
T | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3529A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850166 | ||||||
chr7:55850166
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0007g0224 | 2 | NA18953.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.55-3529A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850166 | ||||||
chr7:55850204
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3567C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850204 | ||||||
chr7:55850207
|
C | T | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55-3570G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850207 | ||||||
chr7:55850236
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-3599A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850236 | ||||||
chr7:55850664
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4027T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850664 | ||||||
chr7:55850755
|
A | C | 63 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.55-4118T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850755 | ||||||
chr7:55850773
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4136A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850773 | ||||||
chr7:55850825
|
C | T | 3 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006 | 3 | HG01123.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.55-4188G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850825 | ||||||
chr7:55850953
|
T | C | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-4316A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55850953 | ||||||
chr7:55851015
|
T | C | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.55-4378A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851015 | ||||||
chr7:55851099
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4462G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851099 | ||||||
chr7:55851233
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4596A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851233 | ||||||
chr7:55851351
|
G | A | 2 | a0001c0001t0006g0083a0001c0001t0006g0097 | 2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.55-4714C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851351 | ||||||
chr7:55851406
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.55-4769G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851406 | ||||||
chr7:55851415
|
G | GTT | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.55-4780_55-4779dup others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851415 | ||||||
chr7:55851415
|
GT | G | 6 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(3): Show | 6 | HG00099.hp2 HG01123.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-4779delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851415 | ||||||
chr7:55851473
|
T | C | 121 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(118): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.55-4836A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851473 | ||||||
chr7:55851518
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4881T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851518 | ||||||
chr7:55851607
|
C | T | 3 | a0001c0001t0016g0204a0001c0001t0016g0243a0001c0001t0034g0189 | 3 | NA18940.hp1 NA18975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.55-4970G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851607 | ||||||
chr7:55851634
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-4997T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851634 | ||||||
chr7:55851667
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5030T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851667 | ||||||
chr7:55851677
|
C | T | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-5040G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851677 | ||||||
chr7:55851681
|
C | T | 1 | a0001c0001t0011g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.55-5044G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851681 | ||||||
chr7:55851734
|
C | T | 12 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0001g0273others(9): Show | 12 | HG00621.hp2 HG02040.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.55-5097G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851734 | ||||||
chr7:55851805
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5168T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851805 | ||||||
chr7:55851824
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5187G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851824 | ||||||
chr7:55851825
|
G | A | 1 | a0001c0001t0004g0385 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.55-5188C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851825 | ||||||
chr7:55851913
|
C | A | 1 | a0001c0001t0004g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.55-5276G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851913 | ||||||
chr7:55851970
|
G | A | 60 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.55-5333C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851970 | ||||||
chr7:55851978
|
T | C | 1 | a0001c0001t0041g0104 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.55-5341A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851978 | ||||||
chr7:55851999
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5362T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55851999 | ||||||
chr7:55852125
|
G | C | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-5488C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852125 | ||||||
chr7:55852139
|
C | CA | 30 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0002g0185others(27): Show | 30 | HG00609.hp2 HG00639.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.55-5503dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852139 | ||||||
chr7:55852139
|
CA | C | 140 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(137): Show | 140 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.55-5503delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852139 | ||||||
chr7:55852142
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5505T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852142 | ||||||
chr7:55852185
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.55-5548A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852185 | ||||||
chr7:55852203
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5566C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852203 | ||||||
chr7:55852226
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5589A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852226 | ||||||
chr7:55852245
|
C | T | 253 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0242others(250): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.55-5608G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852245 | ||||||
chr7:55852341
|
T | C | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-5704A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852341 | ||||||
chr7:55852348
|
C | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5711G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852348 | ||||||
chr7:55852486
|
T | C | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0369 | 3 | NA18968.hp1 NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.55-5849A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852486 | ||||||
chr7:55852526
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-5889A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852526 | ||||||
chr7:55852710
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6073G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852710 | ||||||
chr7:55852721
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6084G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852721 | ||||||
chr7:55852740
|
A | G | 13 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-6103T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852740 | ||||||
chr7:55852791
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.55-6154C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852791 | ||||||
chr7:55852912
|
A | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.55-6275T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852912 | ||||||
chr7:55852971
|
A | G | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.55-6334T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55852971 | ||||||
chr7:55853091
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6454G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853091 | ||||||
chr7:55853092
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6455T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853092 | ||||||
chr7:55853114
|
C | T | 5 | a0001c0001t0006g0073a0001c0001t0006g0074a0001c0001t0006g0143others(2): Show | 5 | HG01993.hp2 HG02257.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-6477G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853114 | ||||||
chr7:55853115
|
G | A | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-6478C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853115 | ||||||
chr7:55853227
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.55-6590G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853227 | ||||||
chr7:55853288
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6651G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853288 | ||||||
chr7:55853335
|
A | T | 124 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.55-6698T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853335 | ||||||
chr7:55853390
|
A | G | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.55-6753T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853390 | ||||||
chr7:55853413
|
A | ATAAGCAA others(36): Show |
1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.55-6819_55-6777dup others(43): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853413 | ||||||
chr7:55853425
|
T | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-6788A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853425 | ||||||
chr7:55853428
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.55-6791T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853428 | ||||||
chr7:55853466
|
C | A | 1 | a0001c0001t0001g0374 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.55-6829G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853466 | ||||||
chr7:55853808
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.55-7171C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853808 | ||||||
chr7:55853841
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-7204C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853841 | ||||||
chr7:55853926
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55-7289C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853926 | ||||||
chr7:55853977
|
A | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-7340T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853977 | ||||||
chr7:55853979
|
A | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-7342T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853979 | ||||||
chr7:55853997
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-7360G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55853997 | ||||||
chr7:55854135
|
T | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-7498A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854135 | ||||||
chr7:55854392
|
CAG | C | 4 | a0001c0001t0010g0012a0001c0001t0010g0015a0001c0001t0010g0016others(1): Show | 4 | HG00673.hp2 HG04228.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+7549_54+7550del others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854392 | ||||||
chr7:55854436
|
CT | C | 77 | a0001c0001t0001g0077a0001c0001t0002g0021a0001c0001t0002g0030others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.54+7506delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854436 | ||||||
chr7:55854452
|
C | G | 1 | a0001c0001t0035g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.54+7491G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854452 | ||||||
chr7:55854460
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+7483G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854460 | ||||||
chr7:55854495
|
T | C | 1 | a0001c0001t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+7448A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854495 | ||||||
chr7:55854522
|
C | T | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.54+7421G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854522 | ||||||
chr7:55854605
|
A | G | 70 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.54+7338T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854605 | ||||||
chr7:55854630
|
A | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.54+7313T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854630 | ||||||
chr7:55854675
|
A | G | 342 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(339): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.54+7268T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854675 | ||||||
chr7:55854714
|
T | C | 1 | a0001c0001t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+7229A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854714 | ||||||
chr7:55854725
|
G | T | 7 | a0001c0001t0004g0001a0001c0001t0004g0110a0001c0001t0004g0125others(4): Show | 8 | HG00639.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+7218C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854725 | ||||||
chr7:55854893
|
T | C | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+7050A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854893 | ||||||
chr7:55854908
|
T | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+7035A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55854908 | ||||||
chr7:55855007
|
C | CT | 34 | a0001c0001t0002g0180a0001c0001t0002g0188a0001c0001t0002g0244others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.54+6935dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855007 | ||||||
chr7:55855007
|
CT | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0269others(34): Show | 37 | HG01981.hp1 HG02056.hp2 HG02132.hp2 others(34): Show |
intron_variant | MODIFIER | c.54+6935delA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855007 | ||||||
chr7:55855007
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0015g0260a0001c0001t0032g0356 | 2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.54+6926_54+6935del others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855007 | ||||||
chr7:55855008
|
T | TTTTTTTT others(571): Show |
72 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0256others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.54+6934_54+6935ins others(578): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855008 | ||||||
chr7:55855008
|
T | TTTTTTTT others(572): Show |
12 | a0001c0001t0001g0250a0001c0001t0001g0266a0001c0001t0001g0299others(9): Show | 12 | HG00408.hp1 HG02027.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+6934_54+6935ins others(579): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855008 | ||||||
chr7:55855009
|
T | TTTTTTTT others(571): Show |
1 | a0001c0001t0001g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.54+6933_54+6934ins others(578): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855009 | ||||||
chr7:55855056
|
C | T | 17 | a0001c0001t0004g0377a0001c0001t0004g0380a0001c0001t0004g0381others(14): Show | 17 | HG00544.hp2 HG00673.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+6887G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855056 | ||||||
chr7:55855057
|
G | A | 2 | a0001c0001t0006g0075a0001c0001t0030g0076 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.54+6886C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855057 | ||||||
chr7:55855077
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6866G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855077 | ||||||
chr7:55855154
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6789C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855154 | ||||||
chr7:55855197
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6746C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855197 | ||||||
chr7:55855355
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6588C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855355 | ||||||
chr7:55855379
|
A | G | 72 | a0001c0001t0001g0242a0001c0001t0002g0014a0001c0001t0002g0147others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.54+6564T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855379 | ||||||
chr7:55855440
|
C | T | 1 | a0001c0001t0005g0371 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.54+6503G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855440 | ||||||
chr7:55855493
|
C | G | 1 | a0001c0001t0006g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.54+6450G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855493 | ||||||
chr7:55855527
|
G | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6416C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855527 | ||||||
chr7:55855584
|
G | C | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+6359C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855584 | ||||||
chr7:55855657
|
G | A | 27 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0002g0234others(24): Show | 27 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.54+6286C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855657 | ||||||
chr7:55855683
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.54+6260C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855683 | ||||||
chr7:55855850
|
G | A | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+6093C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855850 | ||||||
chr7:55855936
|
A | T | 15 | a0001c0001t0002g0014a0001c0001t0004g0377a0001c0001t0004g0380others(12): Show | 15 | HG00544.hp2 HG01358.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.54+6007T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55855936 | ||||||
chr7:55856035
|
T | A | 1 | a0001c0001t0004g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.54+5908A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856035 | ||||||
chr7:55856035
|
T | G | 284 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(281): Show | 284 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.54+5908A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856035 | ||||||
chr7:55856144
|
C | T | 2 | a0001c0001t0012g0270a0001c0001t0012g0302 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.54+5799G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856144 | ||||||
chr7:55856389
|
C | T | 62 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.54+5554G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856389 | ||||||
chr7:55856398
|
C | T | 3 | a0001c0001t0003g0020a0001c0001t0003g0035a0001c0001t0003g0036 | 3 | NA18968.hp2 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.54+5545G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856398 | ||||||
chr7:55856399
|
G | GT | 30 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0269others(27): Show | 30 | HG00609.hp1 HG01175.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.54+5543dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856399 | ||||||
chr7:55856410
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.54+5533C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856410 | ||||||
chr7:55856494
|
C | T | 2 | a0001c0001t0021g0122a0001c0001t0021g0123 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.54+5449G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856494 | ||||||
chr7:55856517
|
G | A | 1 | a0001c0001t0006g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+5426C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856517 | ||||||
chr7:55856526
|
A | G | 348 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(345): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.54+5417T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856526 | ||||||
chr7:55856547
|
A | G | 1 | a0001c0001t0001g0357 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.54+5396T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856547 | ||||||
chr7:55856621
|
G | A | 125 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.54+5322C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856621 | ||||||
chr7:55856684
|
C | T | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+5259G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856684 | ||||||
chr7:55856733
|
C | T | 3 | a0001c0001t0004g0105a0001c0001t0004g0119a0001c0001t0004g0120 | 3 | HG00738.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.54+5210G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856733 | ||||||
chr7:55856740
|
T | G | 64 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0242others(61): Show | 64 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.54+5203A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856740 | ||||||
chr7:55856792
|
G | A | 2 | a0001c0001t0015g0085a0001c0001t0015g0086 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.54+5151C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856792 | ||||||
chr7:55856915
|
T | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+5028A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856915 | ||||||
chr7:55856922
|
C | T | 3 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145 | 3 | HG02257.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.54+5021G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55856922 | ||||||
chr7:55857014
|
A | G | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+4929T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857014 | ||||||
chr7:55857040
|
C | T | 1 | a0001c0001t0014g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.54+4903G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857040 | ||||||
chr7:55857098
|
C | A | 1 | a0001c0001t0003g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.54+4845G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857098 | ||||||
chr7:55857201
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+4742G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857201 | ||||||
chr7:55857202
|
G | A | 12 | a0001c0001t0002g0387a0001c0001t0004g0377a0001c0001t0004g0380others(9): Show | 12 | HG00544.hp2 HG01358.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+4741C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857202 | ||||||
chr7:55857251
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4692T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857251 | ||||||
chr7:55857295
|
C | A | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4648G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857295 | ||||||
chr7:55857297
|
A | G | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4646T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857297 | ||||||
chr7:55857298
|
G | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4645C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857298 | ||||||
chr7:55857302
|
G | C | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4641C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857302 | ||||||
chr7:55857305
|
G | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4638C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857305 | ||||||
chr7:55857340
|
C | A | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4603G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857340 | ||||||
chr7:55857361
|
A | C | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4582T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857361 | ||||||
chr7:55857364
|
C | A | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4579G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857364 | ||||||
chr7:55857393
|
A | AAAGAG | 56 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.54+4545_54+4549dup others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857393 | ||||||
chr7:55857393
|
A | AAAGAGAA others(3): Show |
3 | a0003c0003t0019g0002a0003c0003t0019g0003a0003c0003t0019g0004 | 3 | HG01109.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.54+4540_54+4549dup others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857393 | ||||||
chr7:55857394
|
A | AAGAGAAG others(21): Show |
36 | a0001c0001t0001g0242a0001c0001t0002g0185a0001c0001t0002g0188others(33): Show | 36 | HG00597.hp2 HG02015.hp2 HG02080.hp2 others(33): Show |
intron_variant | MODIFIER | c.54+4521_54+4548dup others(28): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857394 | ||||||
chr7:55857399
|
A | AAGAGAAG others(16): Show |
1 | a0001c0001t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.54+4521_54+4543dup others(23): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857399 | ||||||
chr7:55857403
|
G | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4540C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857403 | ||||||
chr7:55857430
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4513T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857430 | ||||||
chr7:55857431
|
G | A | 12 | a0001c0001t0002g0387a0001c0001t0004g0377a0001c0001t0004g0380others(9): Show | 12 | HG00544.hp2 HG01358.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+4512C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857431 | ||||||
chr7:55857438
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54+4505C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857438 | ||||||
chr7:55857446
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4497T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857446 | ||||||
chr7:55857456
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4487T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857456 | ||||||
chr7:55857460
|
G | A | 344 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(341): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.54+4483C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857460 | ||||||
chr7:55857476
|
A | G | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4467T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857476 | ||||||
chr7:55857485
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4458C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857485 | ||||||
chr7:55857490
|
G | GAGGGA | 100 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0229others(97): Show | 100 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.54+4448_54+4452dup others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857490 | ||||||
chr7:55857490
|
G | GAGGGAAG others(3): Show |
118 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0256others(115): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.54+4443_54+4452dup others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857490 | ||||||
chr7:55857490
|
G | GAGGGAAG others(8): Show |
14 | a0001c0001t0001g0254a0001c0001t0001g0297a0001c0001t0001g0350others(11): Show | 14 | HG02040.hp2 HG02145.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.54+4438_54+4452dup others(15): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857490 | ||||||
chr7:55857490
|
GAGGGA | G | 11 | a0001c0001t0002g0030a0001c0001t0002g0148a0001c0001t0002g0153others(8): Show | 11 | HG00099.hp1 HG00544.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.54+4448_54+4452del others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857490 | ||||||
chr7:55857490
|
GAGGGAAG others(3): Show |
G | 6 | a0001c0001t0006g0087a0001c0001t0006g0089a0001c0001t0006g0090others(3): Show | 6 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+4443_54+4452del others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857490 | ||||||
chr7:55857496
|
A | C | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4447T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857496 | ||||||
chr7:55857505
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4438T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857505 | ||||||
chr7:55857507
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4436C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857507 | ||||||
chr7:55857510
|
A | G | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4433T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857510 | ||||||
chr7:55857517
|
G | GGGAAGGG others(3): Show |
1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54+4425_54+4426ins others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857517 | ||||||
chr7:55857522
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0015g0260a0006c0013t0039g0008 | 3 | HG02922.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.54+4421T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857522 | ||||||
chr7:55857536
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4407T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857536 | ||||||
chr7:55857537
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4406T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857537 | ||||||
chr7:55857541
|
A | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4402T>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857541 | ||||||
chr7:55857545
|
AGGAGG | A | 6 | a0001c0001t0006g0099a0002c0002t0003g0007a0002c0002t0011g0005others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+4393_54+4397del others(5): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857545 | ||||||
chr7:55857545
|
AGGAGGGG others(3): Show |
A | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+4388_54+4397del others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857545 | ||||||
chr7:55857556
|
G | T | 1 | a0001c0001t0003g0029 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54+4387C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857556 | ||||||
chr7:55857569
|
GGGGAGCC others(311): Show |
G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+4056_54+4373del | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857569 | ||||||
chr7:55857582
|
C | CT | 131 | a0001c0001t0001g0077a0001c0001t0001g0229a0001c0001t0001g0237others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.54+4360dupA | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857582
|
C | CTT | 105 | a0001c0001t0001g0242a0001c0001t0001g0250a0001c0001t0001g0252others(102): Show | 105 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.54+4359_54+4360dup others(2): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857582
|
C | CTTT | 54 | a0001c0001t0001g0013a0001c0001t0001g0262a0001c0001t0001g0264others(51): Show | 54 | HG00621.hp2 HG00673.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.54+4358_54+4360dup others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857582
|
CTTT | C | 31 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0153others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.54+4358_54+4360del others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857582
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0357 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.54+4351_54+4360del others(10): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857582
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0018g0358 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.54+4350_54+4360del others(11): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857582 | ||||||
chr7:55857657
|
G | C | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0369 | 3 | NA18968.hp1 NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.54+4286C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857657 | ||||||
chr7:55857814
|
C | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | NA18970.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4129G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857814 | ||||||
chr7:55857831
|
C | G | 2 | a0001c0001t0006g0075a0001c0001t0030g0076 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.54+4112G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857831 | ||||||
chr7:55857867
|
G | A | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+4076C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857867 | ||||||
chr7:55857868
|
C | A | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+4075G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55857868 | ||||||
chr7:55858003
|
C | G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+3940G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858003 | ||||||
chr7:55858435
|
GAAATCAT others(8): Show |
G | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+3493_54+3507del others(15): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858435 | ||||||
chr7:55858642
|
T | TAAA | 6 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+3298_54+3300dup others(3): Show |
SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858642 | ||||||
chr7:55858659
|
T | C | 6 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+3284A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858659 | ||||||
chr7:55858824
|
G | A | 125 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.54+3119C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858824 | ||||||
chr7:55858826
|
G | C | 2 | a0001c0001t0026g0361a0001c0001t0026g0375 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.54+3117C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858826 | ||||||
chr7:55858831
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.54+3112T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858831 | ||||||
chr7:55858895
|
G | A | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.54+3048C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858895 | ||||||
chr7:55858899
|
T | C | 4 | a0001c0001t0027g0102a0001c0001t0027g0103a0001c0001t0035g0101others(1): Show | 4 | HG01891.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+3044A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55858899 | ||||||
chr7:55859017
|
G | C | 1 | a0001c0001t0006g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.54+2926C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859017 | ||||||
chr7:55859108
|
G | A | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+2835C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859108 | ||||||
chr7:55859123
|
C | T | 3 | a0001c0001t0005g0371a0001c0001t0033g0251a0001c0011t0001g0255 | 3 | HG02572.hp2 HG02683.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.54+2820G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859123 | ||||||
chr7:55859151
|
CA | C | 6 | a0001c0001t0001g0254a0001c0001t0002g0148a0001c0001t0002g0185others(3): Show | 6 | HG02040.hp2 HG02698.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+2791delT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859151 | ||||||
chr7:55859210
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.54+2733G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859210 | ||||||
chr7:55859590
|
G | C | 1 | a0001c0001t0005g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54+2353C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859590 | ||||||
chr7:55859628
|
C | G | 125 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.54+2315G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859628 | ||||||
chr7:55859800
|
T | A | 150 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.54+2143A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859800 | ||||||
chr7:55859858
|
A | C | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+2085T>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859858 | ||||||
chr7:55859950
|
C | T | 5 | a0001c0001t0006g0073a0001c0001t0006g0074a0001c0001t0006g0143others(2): Show | 5 | HG01993.hp2 HG02257.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1993G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859950 | ||||||
chr7:55859951
|
G | A | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+1992C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55859951 | ||||||
chr7:55860113
|
AG | A | 35 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.54+1829delC | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860113 | ||||||
chr7:55860179
|
C | CA | 71 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0242others(68): Show | 71 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.54+1763dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860179 | ||||||
chr7:55860302
|
T | C | 12 | a0001c0001t0002g0387a0001c0001t0004g0377a0001c0001t0004g0380others(9): Show | 12 | HG00544.hp2 HG01358.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.54+1641A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860302 | ||||||
chr7:55860314
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+1629C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860314 | ||||||
chr7:55860315
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+1628G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860315 | ||||||
chr7:55860393
|
G | C | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+1550C>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860393 | ||||||
chr7:55860409
|
G | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+1534C>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860409 | ||||||
chr7:55860553
|
T | C | 36 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.54+1390A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860553 | ||||||
chr7:55860669
|
A | G | 8 | a0001c0001t0005g0371a0001c0001t0033g0251a0002c0002t0003g0007others(5): Show | 8 | HG01123.hp2 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+1274T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860669 | ||||||
chr7:55860673
|
C | T | 1 | a0006c0013t0039g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54+1270G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860673 | ||||||
chr7:55860795
|
T | C | 2 | a0001c0001t0005g0371a0001c0001t0033g0251 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.54+1148A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860795 | ||||||
chr7:55860844
|
C | A | 1 | a0001c0001t0002g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.54+1099G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860844 | ||||||
chr7:55860847
|
C | T | 36 | a0001c0001t0001g0077a0001c0001t0006g0011a0001c0001t0006g0073others(33): Show | 36 | HG01243.hp2 HG01433.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.54+1096G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860847 | ||||||
chr7:55860973
|
C | A | 3 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145 | 3 | HG02257.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.54+970G>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55860973 | ||||||
chr7:55861073
|
T | C | 1 | a0001c0001t0006g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.54+870A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861073 | ||||||
chr7:55861238
|
C | T | 62 | a0001c0001t0002g0021a0001c0001t0002g0030a0001c0001t0002g0033others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.54+705G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861238 | ||||||
chr7:55861268
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.54+675G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861268 | ||||||
chr7:55861359
|
A | G | 5 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+584T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861359 | ||||||
chr7:55861439
|
T | C | 35 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.54+504A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861439 | ||||||
chr7:55861501
|
C | CA | 29 | a0001c0001t0001g0242a0001c0001t0001g0372a0001c0001t0001g0374others(26): Show | 29 | HG00408.hp1 HG00544.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.54+441dupT | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861501 | ||||||
chr7:55861556
|
C | G | 1 | a0001c0001t0033g0251 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54+387G>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861556 | ||||||
chr7:55861700
|
G | A | 64 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0242others(61): Show | 64 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.54+243C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861700 | ||||||
chr7:55861731
|
C | T | 1 | a0001c0001t0005g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.54+212G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861731 | ||||||
chr7:55861796
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.54+147T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861796 | ||||||
chr7:55861810
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.54+133A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861810 | ||||||
chr7:55861841
|
T | C | 1 | a0001c0001t0025g0388 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54+102A>G | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861841 | ||||||
chr7:55861846
|
T | A | 150 | a0001c0001t0001g0013a0001c0001t0001g0250a0001c0001t0001g0252others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.54+97A>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 2/9 | chr7 | 55861846 | ||||||
chr7:55862054
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0002g0014a0001c0001t0010g0012others(2): Show | 5 | HG04228.hp1 NA18944.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-43T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/9 | chr7 | 55862054 | ||||||
chr7:55862144
|
C | T | 1 | a0001c0001t0006g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15-133G>A | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/9 | chr7 | 55862144 | ||||||
chr7:55862218
|
T | G | 2 | a0002c0002t0011g0009a0002c0002t0011g0010 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-15-207A>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/9 | chr7 | 55862218 | ||||||
chr7:55862434
|
A | G | 6 | a0002c0002t0003g0007a0002c0002t0011g0005a0002c0002t0011g0006others(3): Show | 6 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+254T>C | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/9 | chr7 | 55862434 | ||||||
chr7:55862459
|
G | A | 1 | a0001c0001t0004g0389 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-16+229C>T | SEPTIN14 | ENSG00000154997.9 | transcript | ENST00000388975.4 | protein_coding | 1/9 | chr7 | 55862459 |